Coordination of cell cycle and morphogenesis during organ formation

Organ formation requires precise regulation of cell cycle and morphogenetic events. Using the Drosophila embryonic salivary gland (SG) as a model, we uncover the role of the SP1/KLF transcription factor Huckebein (Hkb) in coordinating cell cycle regulation and morphogenesis. The hkb mutant SG exhibits defects in invagination positioning and organ size due to the abnormal death of SG cells. Normal SG development involves distal-to-proximal progression of endoreplication (endocycle), whereas hkb mutant SG cells undergo abnormal cell division, leading to cell death. Hkb represses the expression of key cell cycle and pro-apoptotic genes in the SG. Knockdown of cyclin E or cyclin-dependent kinase 1, or overexpression of fizzy-related rescues most of the morphogenetic defects observed in the hkb mutant SG. These results indicate that Hkb plays a critical role in controlling endoreplication by regulating the transcription of key cell cycle effectors to ensure proper organ formation.


Introduction
The formation of tubular organs, such as the lungs and kidneys, begins with the folding of flat epithelial tissues into functional three-dimensional (3D) tubular structures.In humans, errors in tube formation can result in congenital defects such as spina bifida and lung hypoplasia (Wilde et al., 2014).Studies in both vertebrates and invertebrates have revealed key morphogenetic mechanisms underlying epithelial tube formation during development (Andrew and Ewald, 2010;Chung et al., 2014;Herriges and Morrisey, 2014;Girdler and Röper, 2014;Nikolopoulou et al., 2017;Spina and Cowin, 2021;Pradhan et al., 2023).While proper cell shape changes and cell rearrangement are critical, precise regulation of cell division and cell death is also essential for tissue morphogenesis (Huh et al., 2004;Mao et al., 2013;LeGoff and Lecuit, 2015;Godard and Heisenberg, 2019).Notably, the interplay between cell division and cell death provides a homeostatic control system necessary for proper organ formation.Perturbations at any stage of the cell cycle can have detrimental effects on cell viability, leading to cell death, and activation of apoptosis can trigger compensatory proliferation in surrounding cells (Ryoo et al., 2004).In addition to their role in establishing and maintaining the correct number of cells in tissues and organs, cell division and cell death generate biophysical forces through actomyosin reorganization that help shape the final tissue morphology.For example, during Drosophila tracheal invagination, mitotic cell rounding drives the internalization of the tracheal primordium (Kondo and Hayashi, 2013).During dorsal closure and leg folding in Drosophila (Toyama et al., 2008;Monier et al., 2015) and neural closure in mammals (Massa et al., 2009;Yamaguchi et al., 2011), apoptotic cells generate forces at both local and tissue scales that affect tissue remodeling.Therefore, to fully understand the mechanisms of organ formation, it is critical to know how the cell cycle, cell death, and morphogenesis are coordinated during epithelial tube formation.
The Drosophila embryonic SG is a premier model for studying the mechanisms of tube formation from a flat epithelial sheet (Chung et al., 2014;Sidor and Röper, 2016).The Drosophila embryo contains two SGs, each consisting of 140-150 cells, which initially reside on the embryo surface and invaginate to form single-layered, elongated tubes (Figure 1A).Once SG cells are specified, they do not divide or die.Cell death is actively inhibited during SG morphogenesis.The SG-upregulated transcription factors Fork head (Fkh), Senseless, and Sage inhibit apoptosis by downregulating proapoptotic genes, such as head involution defective (hid) and reaper (rpr) (Myat and Andrew, 2000a;Chandrasekaran and Beckendorf, 2003;Fox et al., 2013).Instead of cell division, SG cells undergo endoreplication (endocycle), a variant of the cell cycle that involves DNA replication without subsequent cell division forming polyploid cells, upon invagination at stage 11 (Follette et al., 1998).SG cells that have completed one round of endoreplication arrest the cell cycle in G2 until the larval stage (Smith and Orr-Weaver, 1991;Chandrasekaran and Beckendorf, 2005).Endoreplication, which is more common in invertebrates and plants, was thought to be a rare cell cycle variation in mammals.However, recent studies have revealed endoreplication in various mammalian tissues, including humans, and endoreplication is emerging as a potential developmental timer (Gandarillas et al., 2018).Like the conventional cell cycle, endoreplication is regulated by key cell cycle genes such as cyclins and cyclin-dependent kinases (CDKs).In Drosophila embryogenesis, re-entry into S phase during endoreplication is regulated by the cyclin E-Cdk2 complex through the E2F proteins (Duronio et al., 1995;Follette et al., 1998).Because SG morphogenesis occurs in the absence of cell division and cell death, studies of SG morphogenesis have primarily focused on the mechanisms underlying cell shape changes, cell intercalation, and collective cell migration (Pirraglia et al., 2010;Xu et al., 2011;Röper, 2012;Ismat et al., 2013;Booth et al., 2014;Chung et al., 2014;Chung et al., 2017;Sanchez-Corrales et al., 2018;Sánchez-Corrales et al., 2021;Le and Chung, 2021;Vishwakarma et al., 2022).Little is known about the potential impact of regulating endoreplication and cell death during SG morphogenesis.
Invagination is the first step in SG morphogenesis that is critical for organ architecture, and studies in recent years have revealed key underlying molecular and cellular mechanisms (Chung et al., 2017;Sanchez-Corrales et al., 2018;Sidor et al., 2020;Sánchez-Corrales et al., 2021;Le and Chung, 2021;Vishwakarma et al., 2022).SG invagination occurs in a stereotypical manner, with two predominant cell behaviors occurring in distinct spatial domains within the placode relative to the invagination pit forming in the dorsal/posterior region: clustered apical constriction near the pit (Figure 1A) and cell intercalation far from the pit.Two early-expressed SG-upregulated transcription factors, Fkh and Hkb, play critical roles in SG invagination.Fkh, a winged-helix transcription factor that regulates more than two-thirds of the known SG genes, is essential for SG invagination; SG cells fail to invaginate in fkh mutants in which apoptosis is inhibited (Myat and Andrew, 2000a;Maruyama et al., 2011).Hkb, an SP1/KLF transcription factor, is crucial for invagination positioning; SG cells invaginate in the central region of the placode in hkb mutants (Myat and Andrew, 2000b).A recent study proposed that the early patterning of Fkh and Hkb and their downstream effectors ensures positionally fixed cell behaviors with respect to invagination position (Sánchez-Corrales et al., 2021).For example, a key downstream target of Fkh, Folded gastrulation (Fog), signals through its G protein-coupled receptor to activate Rho kinase and myosin to regulate apical constriction in the dorsal/posterior region of the SG placode (Chung et al., 2017;Vishwakarma et al., 2022).Despite the intriguing phenotype of hkb mutants, the mechanism of how Hkb regulates SG invagination positioning remains largely unknown.Only two potential downstream targets of Hkb involved in SG formation have been identified: crumbs (crb), encoding a key apical membrane protein, and klarsicht (klar), encoding a Nesprin family protein that mediates dynein-dependent organelle trafficking (Myat and Andrew, 2002).To fully understand the mechanism of how Hkb regulates invagination position, it is critical to reveal the precise cellular mechanisms underlying the centered invagination phenotype and identify Hkb downstream targets regulating the process.In this study, we reveal the distal-to-proximal progression of endoreplication during SG morphogenesis and show that Hkb plays a critical role in this process.Loss of hkb results in abnormal cell division in the SG leading to cell death.Subsequently, abnormal cell death leads to malposition of the SG invagination and the formation of a smaller organ.Using modENCODE Hkb ChIP-Seq targets and genetic interaction analyses, we show that Hkb represses the transcription of key cell cycle genes in the SG to control cell cycle progression and ensure cell survival and proper SG morphogenesis.

Creation of the molecularly defined hkb mutant alleles and fluorescent knock-in lines
To fully characterize the role of Hkb during SG morphogenesis, we generated two nulls (hkb 351 , hkb 391 ) and two hypomorphic alleles (hkb 121 , hkb 131 ) using CRISPR/Cas9 (Figure 1B; Details of indels and expected protein sequences were described in Figure 1-figure supplement 1).All alleles were embryonic lethal in homozygous embryos and transheterozygotes with a deficiency line deleting the hkb locus, suggesting that all three zinc-finger (ZnF) domains are required for embryonic development and survival.Immunostaining with CrebA, a nuclear marker for secretory cells of the SG, and E-Cadherin (Ecad), an adherens junction marker, showed that wild-type (WT) embryos exhibited SG invagination in the dorsal-posterior region of the placode (Figure 1C).However, new hkb alleles exhibited a broad, central SG invagination phenotype (Figure 1D and E), similar to previous studies with an EMS allele hkb 2 and a P-element excision allele hkb A321R1 (Weigel et al., 1990;Gaul and Weigel, 1990;Myat and Andrew, 2002;De Iaco et al., 2006;Sánchez-Corrales et al., 2021).hkb 121 also exhibited the centered invagination phenotype, albeit with only 50% penetrance (Figure 1D; n=20), indicating that all three ZnF domains are required for the positioning of the SG invagination.
We also generated two mCherry-tagged transgenic lines, Hkb WT -mCh (a functional fusion protein line) and Hkb mut -mCh (a mutant knock-in line) using CRISPR-mediated homology-directed repair (Figure 1B).The Hkb WT -mCh line exhibited nuclear mCh signals in several tissues known to express Hkb, including the anterior and posterior termini of the early embryo, SGs, and a subset of neuroblasts (Figure 1F and F' and Figure 1-figure supplement 2).In the SG, strong Hkb WT -mCh signals were detected at stages 10 and 11, with higher levels in the posterior region of the placode at stage 10 (Figure 1-figure supplement 2C-F"), consistent with a previous study (Sánchez-Corrales et al., green and gRNAs used for hkb alleles and mCh knock-in lines.Bottom: Hkb protein structures produced in each allele and knock-in lines.In hkb 121 , two amino acids (N237 and E238) are substituted with K237 (asterisk).In hkb 351 and hkb 391 , a short N-terminal region of the Hkb protein (green) is followed by random amino acid sequences (blue) due to a frameshift.hkb mRNA with the premature stop codon in hkb 351       To investigate the effect of hkb loss on SG cell behavior during invagination at stage 11, we analyzed the distribution of SG cells undergoing apical constriction in WT and hkb mutants using cell segmentation analysis (Figure 1H-K' and Figure 1-figure supplement 3).Before invagination, WT SG cells with small apical areas clustered in the dorsal-posterior region of the placode, whereas hkb mutants exhibited a scattered distribution (Figure 1-figure supplement 3D-F').As invagination progressed, more cells with small apical areas were observed near the invagination pit in WT, whereas these cells were distributed around the wide central pit in hkb mutant SGs (Figure 1H-J').This is consistent with a previous study using hkb 2 (Sánchez-Corrales et al., 2021), although we observed that only about 30% of the hkb 2 embryos showed the central SG invagination phenotype (n=11).The frequency distribution of cells based on their apical areas showed a significantly lower percentage of SG cells with smaller apical areas in hkb mutants compared to WT (Figure 1K and K' and Figure 1figure supplement 3G, G'), indicating a defect in apical constriction.
Using CrebA signals, we analyzed SG morphology in late-stage WT and homozygous hkb mutant embryos, as well as hkb transheterozygous embryos over a deficiency line deleting the hkb locus.At stage 12, while the WT SGs turned and migrated toward the posterior of the embryo upon reaching the visceral mesoderm, SGs in hkb mutant embryos migrated only slightly posteriorly (Figure 1L-N and Figure 1-figure supplement 4A-E).Consistent with the role of Hkb in endoderm specification (Brönner et al., 1994), hkb mutant embryos showed defects in gut morphology, as well as defects in head development and occasional defects in germ band retraction (Figure 1L'-N' and Figure 1figure supplement 4B'-E'), making it difficult to determine their correct stage after stage 14.Stage 15+ embryos in hkb mutants formed small SGs compared to stage 15 WT embryos (Figure 1L'-N' and Figure 1-figure supplement 4A-E'), as in a previous study (Myat and Andrew, 2000b).We observed a range of SG lengths.More than 40% of stage 15+ hkb null embryos and transheterozygotes of null over a deficiency (hkb 351 , hkb 391 , and hkb 351 /Df) exhibited very short and ball-like SGs (Figure 1N In all hkb mutant lines, one or both SGs frequently mislocalized anteriorly, toward the head center region .Using the salivary duct marker Dead Ringer (Dri; Gregory et al., 1996) and Ecad, we found that the mispositioning of the SG may be due, at least in part, to the defects of the duct, likely resulting from a combination of reduced cell number, aberrant apical domain size, and defective cell intercalation of duct cells (Figure 1figure supplement 5A-K').We also found a transient Hkb expression in the SG duct at early stage 11 (Figure 1-figure supplement 5L-M'), suggesting a possible role of Hkb during SG duct morphogenesis.
Together, we have generated molecularly defined null and hypomorphic alleles of hkb and fluorescently tagged knock-in transgenic lines.Since the two null and two hypomorphic alleles behaved similarly, we used hkb 351 and hkb 121 for further analyses.

Hkb is required for SG cell survival to ensure proper organ size
To determine the cellular mechanisms underlying the small SG phenotype in hkb mutant embryos, we measured the SG lumen length and counted SG cells using Ecad and CrebA signals, respectively.Compared to WT, hkb null mutants and transheterozygous hkb null over a deficiency showed a significantly shorter SG lumen length, and hkb hypomorphic embryos showed a milder effect (Figure 2A-D  and G).Surprisingly, hkb null mutants also showed fewer SG cells compared to WT, with a moderate   and G'').The effect was milder in hypomorphic embryos (Figure 2G' and G''), indicating a correlation between the SG lumen length and the number of cells.
To test whether hkb mutant SG cells undergo apoptosis, we labeled WT, hkb mutant, and Hkb WT -mCh and Hkb mut -mCh embryos with an antibody against Drosophila cleaved death caspase-1 (DCP-1; Sarkissian et al., 2014).WT and Hkb WT   (Zamzami and Kroemer, 1999).At stages 13 and 14, several fragmented cells positive for DCP-1 and mCh, and negative for CrebA, were found near the SG in Hkb mut -mCh embryos (Figure 2R-R''; Figure 2-figure supplement 1D-E").Similar DCP-1positive cells were found near the SG in hkb null mutants, fewer in hkb hypomorphs, and rarely in WT embryos (Figure 2-figure supplement 1F-H').These cells, lacking CrebA signals but exhibiting nuclear fragmentation and condensation, are likely late-stage apoptotic SG cells.Dying cells were also observed in other parts of the Hkb mut -mCh embryos near mCh-expressing regions compared to Hkb WT -mCh embryos (Figure 2-figure supplement 1I-K"), as well as some hkb mutant SG duct cells (Figure 1-figure supplement 5E, E'), which may be the cause of the decreased duct cell numbers.This suggests a role for Hkb in cell survival in multiple cell types.
We next performed a rescue experiment.Consistent with a previous study (Myat and Andrew, 2002), overexpression of Hkb in SG secretory cells using the fkh-Gal4 driver (Henderson and Andrew, 2000) in the otherwise WT background had no overt effects on SG formation, except for an expanded SG lumen at late stages.Overexpression of Hkb in the SG in hkb mutants almost completely rescued the short SG phenotype of hkb mutants, resulting in elongated SGs that resembled WT SGs (Figure 2F; Figure 2-figure supplement 2C-E, K), with a reduced number of DCP-1-positive SG cells (Figure 2L and P), and restored lumen length and SG cell number to WT levels (Figure 2E and G'').Additionally, blocking apoptosis in the hkb mutant SG by overexpressing the baculoviral protein p35, a caspase inhibitor of apoptosis, reduced the number of DCP-1-positive cells (Figure 2M and P) and rescued the shortened SG phenotype, with restored SG cell number (Figure 2G''; Figure 2-figure supplement 2F-I, K).These data suggest that the small SG size in hkb mutants is primarily caused by the apoptosis of SG cells.

Hkb is required for apical domain elongation
A previous study showed that hkb regulates apical domain elongation by regulating the key apical protein Crb and the endocytic pathway regulator Klar (Myat and Andrew, 2002).Although our data showed that the reduced number of SG cells is the main reason for the small gland size in hkb mutants, defects in apical domain elongation may also contribute to this phenotype.Measuring the apical area of individual SG cells in stage 15 embryos revealed that hkb mutant SG cells have smaller apical domain sizes than WT (Figure 2-figure supplement 3A-E).Immunostaining with Rab11, a recycling endosome marker, revealed that while WT SGs showed Rab11 signals near the apical domain, hkb mutant SGs displayed basally mislocalized Rab11 signals (Figure 2-figure supplement 3F-G').These data suggest that impaired apical trafficking and defective apical membrane elongation also contribute to the small gland phenotype in hkb mutants.

Aberrant cell death causes centered SG invagination in hkb mutants
Next, we tested invagination positioning.SG-specific expression of Hkb corrected the centered invagination defect in hkb mutants (Figure 3A-C), indicating a tissue-autonomous role of Hkb in SG invagination positioning.Interestingly, blocking apoptosis in the SG also rescued the centered   invagination phenotype in hkb mutants (Figure 3D).In these embryos, cells with small apical areas were mainly distributed in the dorsal/posterior quadrant of the SG placode (Figure 3E-F'), as in WT (Figure 1H and H').SG-specific Hkb overexpression partially rescued the apical constriction defects, and although not statistically significant, blocking apoptosis also slightly decreased the number of SG cells with small apical areas in hkb mutants (Figure 3G and G').Since apoptotic cells undergo apical constriction before being eliminated from the epithelial sheet (Toyama et al., 2008;Slattum et al., 2009;Marinari et al., 2012), we hypothesized that some SG cells with small apical areas in hkb mutants are apoptotic.In support of this, we observed DCP-1-positive cells with reduced apical areas in hkb mutant SGs at stage 11 (Figure 3H).Among the SG cells of lower 30% of apical areas, more than 40% were DCP-1-positive (n=29/72 cells in five SGs from different embryos).We did not detect a significant spatial bias in the distribution of DCP-1-positive cells among the four quadrants of the SG placode in hkb null mutants, although slightly more DCP-1-positive cells were observed in the posterior region in hypomorphs and transheterozygotes of null over deficiency (Figure 3I-J).When we analyzed the SG placode in three domains (inner, outer, and mid), we found that most DCP-1-positive cells were in the mid domain, especially in the null and transheterozygous conditions (Figure 3J').This suggests a correlation between the distribution of dying cells in the mid-domain and the widened central invagination pit observed in hkb mutants.
During apoptosis, the cytoskeleton actively participates in the morphological changes of dying cells.Apoptotic cells also exert a transient pulling force on the apical surface, generating the apicobasal force and increasing tissue tension (Monier et al., 2015).Therefore, we analyzed filamentous actin (F-actin) and myosin using phalloidin and sqh-GFP, a functional tagged version of the myosin regulatory light chain (Royou et al., 2004), respectively, in WT and hkb mutant SGs.Compared to WT, we often observed an aberrant accumulation of F-actin and myosin signals along multiple junctions within the SG placode in hkb mutants (Figure 3K-O'').In addition, there was placode-wide disruption of myosin, including the misshapen supracellular myosin cable that maintains SG tissue integrity (Figure 3L).Apical junctions with increased myosin or F-actin levels often coincided with DCP-1positive cells (Figure 3M-M'' and N-O'').Increased F-actin expression was also seen at the apicallateral membrane of DCP-1 positive cells (Figure 3O), suggesting a potential pulling force along the apicobasal axis by apoptotic cells.

Hkb is required for the proper cell cycle status of the SG cells
To further test the impact of hkb loss in cytoskeletal organization, we analyzed microtubules, which play a crucial role in forming and maintaining the actomyosin network during tissue invagination (Booth et al., 2014;Ko et al., 2019;Le and Chung, 2021).Interestingly, immunostaining with an antibody against tyrosinated α-tubulin (Tyr-tub), which labels dynamic, short-lived microtubules (Westermann and Weber, 2003) revealed that, in contrast to the strong Tyr-tub signals observed at the apices of WT SG cells (Figure 4A and A'; Booth et al., 2014;Le and Chung, 2021), some SG cells in hkb mutants lacked apical Tyr-tub signals (Figure 4B and B').These cells had large, rounded morphology and mislocalized nuclei near the apical surface (Figure 4C and D), indicating cell division.Staining with an antibody against phosphorylated histone H3 (PH3), a marker of mitotic chromatin modification (Gurley et al., 1978), revealed strong PH3 signals in hkb mutant SG cells (Figure 4E-H and M), indicating that these cells are actively dividing.Co-staining with Tyr-tub and PH3 revealed that mitotic   spindles were consistently aligned parallel to the epithelial sheet (Figure 4K and K'; n=35 cells in metaphase and anaphase in 16 SGs).
Mitotic cell rounding and cytokinesis employ processes that reorganize the cytoskeleton, generating forces that locally affect cell rearrangement and tissue morphogenesis (Champion et al., 2017;Pinheiro and Bellaïche, 2018).We observed an increase in F-actin along the apical junctions in PH3positive SG cells (Figure 4L).Increased F-actin signals were also often detected along the apical-lateral membrane in PH3-positive cells and along the entire membrane of cells in prophase (Figure 4L-L''; red arrowheads in inset).While no biased distribution of dividing cells was observed across the SG placode in hkb mutants, dividing cells were more frequently localized in the mid-domain compared to the inner or outer domain of the SG (Figure 4N and O).SG-specific expression of Hkb in hkb mutants reduced the number of PH3-positive cells significantly (Figure 4I and M), suggesting a role for Hkb in inhibiting the mitotic entry of SG cells.
Given that apoptosis can induce compensatory cell proliferation in neighboring cells to maintain tissue homeostasis (Haynie and Bryant, 1977;Kondo et al., 2006;Crucianelli et al., 2022), we investigated whether the abnormal cell division in hkb mutants was a result of apoptosis.The number of PH3-positive cells in p35-overexpressing SGs in hkb mutants was comparable to that in hkb mutants alone (Figure 4J and M), suggesting that the abnormal cell division in hkb mutants may not be compensatory cell proliferation induced by apoptosis.However, we cannot rule out the possibility that compensatory cell proliferation by a few remaining dying cells still contributes to some of the abnormally dividing cells in hkb mutants.

Hkb regulates endoreplication progression during SG morphogenesis
The observation of cell division in SG cells was unexpected because SG cells do not divide but rather undergo endoreplication.To further test the cell cycle status in SG cells, we used the Fly-FUCCI system, which allows the identification of different cell cycle phases based on the fluorescent signals of cytoplasmic cyclin B (CycB) and nuclear E2F transcription factor 1 (E2f1) tagged degrons (Zielke et al., 2014;Figure 5A) In hkb mutant SGs, the distal-to-proximal progression of endoreplication was disrupted.It is of note that EdU signals in hkb mutants were generally low in the entire embryo and absent in many tissues compared to WT, suggesting endoreplication defects in multiple tissues upon hkb loss (Figure 5 (Jackman et al., 1995).However, starting at late stage 11 and throughout all stages, almost all SG cells in hkb mutants showed nuclear E2f1 signals of varying intensity (Figure 5G-G'', K-K'' and O-O'').Consistent with this, a few randomly distributed SG cells in hkb mutants showed variable EdU signals, with no clear pattern as seen in WT SGs (Figure 5E, I, M and Q), suggesting that cells either do not enter S phase   or enter a weak S phase.Taken together, Hkb plays a critical role in distal-to-proximal endoreplication progression during SG morphogenesis.

Regulation of key cell cycle genes by Hkb is critical for cell survival and SG morphogenesis
To understand the mechanisms of endoreplication regulation during SG morphogenesis, we focused on the direct transcriptional targets of Hkb identified by the modENCODE Project using chromatin immunoprecipitation followed by sequencing (ChIP-seq) on the whole embryo (Roy et al., 2010).Gene Ontology enrichment analysis revealed several key biological processes associated with the defects observed in hkb mutants (Figure 6A).Notably, gene clusters related to the cell cycle were identified, including central players like Cyclin A (CycA), Cyclin D (CycD), Cyclin E (CycE), E2f1, aurora A (aurA), and aurora B (aurB).Additionally, several apoptosis-related genes were identified, including hid, rpr, and Death related ICE-like caspase (Drice).The full list of Hkb target genes, GO clusters, and the list of genes in each cluster were included in Supplementary file 3. Fluorescence in situ hybridization revealed a significant increase in the mRNA levels of rpr, E2f1, and CycE in hkb mutant SGs compared to WT at stages 11 and 12 (Figure 6B-J, and Figure 6-figure supplement 1A-H'), suggesting transcriptional repression of these genes by Hkb.CycA mRNA levels were increased in some stage 11 SG cells in hkb mutants, whereas all WT SG cells of the same stage showed a background level of CycA mRNA signals (Figure 6-figure supplement 1I-J').
Although not a target of Hkb based on the Chip-seq data, we also tested to see if hkb acts as an indirect transcriptional inhibitor of string (stg), which encodes Cdc25 family protein phosphatase that dephosphorylates and activates Cdk1, triggering entry into mitosis in a post-blastoderm Drosophila embryo (Edgar and O'Farrell, 1989;Gautier et al., 1991;Edgar et al., 1994).Consistent with a previous study (Edgar et al., 1994), stg mRNA levels were downregulated in the WT SG once invagination began, and this remained true for the hkb mutant SG (Figure 6-figure supplement 1K-M), suggesting that the abnormal cell cycle regulation in hkb mutants is not due to upregulation of stg mRNA levels.
Disruption in cell cycle regulation can lead to apoptosis due to errors in DNA replication or failure of DNA integrity checkpoints (Pucci et al., 2000).Immunostaining with a marker of DNA double-strand breaks (γ-H2Av; Lake et al., 2013) showed increased levels in hkb mutant SGs compared to WT, indicating increased DNA damage (Figure 6-figure supplement 2A-B').To test whether apoptosis in hkb mutant SG cells was triggered by the dysregulation of cell cycle genes, we analyzed double mutants for hkb and each of the key Hkb target cyclins and their interacting Cdk genes (Cdk1 and Cdk2).Embryos single mutant for CycA, CycD, CycE, and Cdk1 showed relatively normal morphology except for a few PH3-positive SG cells in CycD and CycE mutants, likely due to disrupted cell cycle and abnormal entry into mitosis (Figure 6-figure supplement 3A-F).Embryos double mutant for hkb and CycE or Cdk1 rescued the hkb mutant phenotypes, but double mutants for hkb and CycA did not show significant rescue (Figure 6-figure supplement 3I-M, P, Q).Cdk2 mutant embryos showed severe morphological defects with significantly fewer cells overall, making it difficult to assess differences in the hkb mutant background (Figure 6-figure supplement 3G, H).We confirmed the rescue effect by SG-specific knockdown experiments targeting CycE and Cdk1 in hkb mutant SGs.As in the double mutant analysis, the knockdown of CycE resulted in a reduction of both dividing and dying cells (Figure 6K, N and Q), restored the invagination position and led to a partial rescue of the short SG phenotypes (Figure 6K and N; Figure 6-figure supplement 4K-N, AB).Similar rescue effects were observed with Cdk1 knockdown (Figure 6L, O, Q

and R and Figure 6-figure supplement 4O-R, AB).
To further test Hkb's role in cell cycle regulation, we tested Fizzy-related (Fzr), a cell cycle switch that functions with the anaphase-promoting complex (APC) to degrade mitotic cyclins during M and G1 phases and trigger exit from the M phase (Sigrist and Lehner, 1997).Fzr also regulates the transition from the normal cell cycle to the endocycle by degrading mitotic cyclins during G2 phase (Sigrist and Lehner, 1997;Zielke et al., 2011).fzr was not a ChiP-Seq target of Hkb, and the fzr mRNA levels in the SG were fairly high in both WT and hkb mutant embryos.We hypothesized that further overexpression of Fzr in hkb mutant SGs could suppress cell division and cell death and rescue the defective tube length phenotype.In support of our hypothesis, overexpression of Fzr in hkb mutant SGs resulted in a reduction of both dividing and dying cells, partially rescuing the overall hkb mutant       supplement 4S-V, AB).When both Fzr and p35 were overexpressed in the hkb mutant background to inhibit both mitotic cyclins and cell death, we observed an enhanced rescue effect (Figure 6-figure supplement 4W-Z, AB).Overall, these data suggest that the loss of hkb leads to the derepression of cyclin/Cdk activities, which disrupts endoreplication and causes SG cells to enter mitosis abnormally (Figure 7).Consequently, cell death occurs in SG cells, leading to disrupted SG morphology.

Discussion
In this study, we have uncovered a previously uncharacterized role for Hkb in coordinating cell cycle regulation and morphogenesis during development.Through a comprehensive analysis of mutant phenotypes, modENCODE ChIP-Seq targets of Hkb, and genetic interaction analyses, we have revealed the role of Hkb in regulating endoreplication to enable the proper development of the SG.

Hkb regulates the cell cycle through transcriptional and possibly posttranslational mechanisms
During Drosophila embryonic development, many tissues arrest the cell cycle in the G2 phase after the initial cell divisions (Hartenstein and Campos-ortega, 1985;Edgar and O'Farrell, 1989).Subsequently, several tissues, including the SG, switch to the endocycle.This switch is correlated with the development of three-dimensional organs, suggesting a metabolic need to inhibit active cell proliferation to allow for such a transition during development.Using the Fly-FUCCI system and EdU labeling, we observed progressive endoreplication from distal to proximal regions during normal SG morphogenesis (Figure 5).Our data are consistent with a previous study showing that distal cells enter S phase first during SG invagination (Chandrasekaran and Beckendorf, 2005).Notably, our observation that some distal SG cells in WT re-enter S phase during late SG morphogenesis suggests a potential second wave of endoreplication toward the end of embryogenesis that has not been described.In hkb mutant SGs, progressive endoreplication is lost.
We propose that endoreplication in SG cells is regulated, at least in part, by Hkb-mediated transcriptional repression of E2f1 and CycE (Figure 6 and Figure 6-figure supplement 1).E2f1 is usually destroyed as cells transit into S phase through degradation by the S-phase activated E3 ubiquitin ligase Cullin 4. Whenever E2f1 expression persists in S phase, as is seen with ectopic expression or overexpression of E2f1, cell cycle arrest is disrupted and the rate of cell cycle progression is increased, leading to a significantly higher number of cells in the mitotic phase (Neufeld et al., 1998;Shibutani et al., 2008), as we observed in the hkb mutant SG.The changes in the cell cycle control mechanism caused by persistent E2f1 expression during the S phase ultimately lead to widespread apoptosis in affected tissues (Shibutani et al., 2008).During normal SG development, E2f1 and CycE (which is also a transcriptional target of E2f1; Ohtani et al., 1995;Duronio and O'Farrell, 1995;Royzman et al., 1997;Duronio et al., 1998) may together control the transition to S phase to begin endoreplication.We propose that Hkb promotes SG cell progression through the S phase, at least in part, through its repression of E2f1 and CycE expression.In support of this, knockdown of CycE partially rescued the hkb mutant phenotypes (Figure 6).
Notably, stg transcript levels remain low in hkb mutant SGs, suggesting that the abnormal mitotic entry of hkb mutant SG cells is not due to stg upregulation.We propose that Hkb prevents entry into mitosis, at least in part, by downregulating CycA expression.CycA acts in the Drosophila G2/M phases of the cell cycle, where it regulates aspects of the DNA replication mechanism and entry into mitosis by binding to Cdk1 (Pagano et al., 1992;Knoblich et al., 1994;Yam et al., 2002;Gong and Ferrell, 2010;Bendris et al., 2011;Sallé et al., 2012).Loss of hkb may prevent inhibition of CycA-Cdk1 activity in the SG.In support of this idea, the knockdown of Cdk1, or overexpression of Fzr, an inhibitor of mitotic cyclins, partially rescued the hkb mutant phenotypes (Figure 6).Depletion of the zygotic CycA pool did not rescue the hkb mutant phenotypes, either because of the contribution of the maternal CycA pool or because of the presence of CycB and CycB3, two other cyclins that bind to Cdk1 to regulate mitotic entry.
Hkb may regulate the cell cycle not only through transcriptional control of cell cycle genes but also by influencing ubiquitination, a key mechanism of cell cycle regulation.ChIP-Seq analysis revealed that Hkb targets several key components involved in ubiquitination, including cullin 1 and archipelago (ago) (Figure 6A; Supplementary file 3).Ago is known to regulate CycE levels in Drosophila (Moberg et al., 2001).Remarkably, ZnF transcription factors can interact with both nucleic acids and proteins and are important regulators of protein degradation through ubiquitination (Gibson et al., 1988;Iuchi and Kuldell, 2005).Further studies will provide a deeper understanding of the comprehensive mechanisms by which Hkb regulates the cell cycle.

Progressive endoreplication during organ formation
Endoreplication in the Drosophila embryonic SG, coupled with invagination, allows cells to increase the number of gene copies to provide sufficient proteins for morphogenesis.The regulatory mechanism behind the progressive distal-to-proximal endoreplication in the SG remains unclear.In agreement with Sánchez-Corrales et al., 2021, we observed higher levels of Hkb in the posterior region of the placode at stage 10, which became more uniformly distributed throughout all SG cells by stage 11 (Figure 1-figure supplement 5).The initial difference in Hkb levels within the SG placode may lead to the differential repression of cell cycle genes, contributing to the progression of endoreplication.Alternatively, SG invagination in the dorsal/posterior region could potentially trigger the sequential onset of endoreplication, as suggested by a previous study (Chandrasekaran and Beckendorf, 2005).We observed a disruption in the progressive entry of the SG cells into endoreplication when Hkb function is lost.The degree of disruption varied between samples, with some embryos showing no SG cells in S phase, while others had a small number of SG cells at random positions along the proximal-distal axis with weaker EdU signals compared to WT SGs of similar stages, suggesting that they may be entering a weak S phase (Figure 5).Further investigation of the relationship between endoreplication regulation and SG invagination will provide a better understanding of how cell cycle and morphogenesis coordinate during organ formation.It will also be interesting to test a role for Hkb in cell cycle (endocycle) regulation in other Drosophila tissues, and to test a similarly conserved role for the mammalian SP/KLF transcription factors.

Hkb's roles in cytoskeletal reorganization and intracellular trafficking
In line with previous studies on the cellular forces exerted by dividing (Kondo and Hayashi, 2013;Pinheiro and Bellaïche, 2018) and apoptotic (Monier et al., 2015;Toyama et al., 2008) cells on neighboring cells, the abnormal cell division, and excessive cell death observed in hkb mutant SGs are associated with a tissue-wide disruption of actomyosin and cell geometry (Figure 3).Our data show that the centralized invagination phenotype results primarily from excessive cell death (Figure 2 and Figure 3).However, dividing cells, particularly those near the SG boundary, may contribute to this phenotype by undergoing cell surface area expansion during cell division, increasing the number of cells with larger apical areas along the SG boundary (Figure 4).
Based on Hkb ChIP-Seq targets, we propose that Hkb also plays an active role in regulating cytoskeletal organization through transcriptional regulation of key cytoskeletal regulators.Hkb targets include key Rho signaling components and their regulators, such as the small GTPases Rho1 and Rac1, and several RhoGEFs, including RhoGEF2, a key activator of Rho signaling during epithelial morphogenesis (Barrett et al., 1997;Figure 6A; Supplementary file 3).We also propose a critical role for Hkb in regulating intracellular trafficking.Supporting previous research on Hkb's role in regulating Klar, an important regulator of intracellular trafficking (Myat and Andrew, 2002), our data show that Rab11 is mislocalized basally in hkb mutant SGs (Figure 2-figure supplement 2).Multiple endocytic components, including βCOP, AP-1-2β, AP-2α, and Nuf, as well as several Rab GTPases, including Rab4, Rab10, Rab27, and Rab30, were also identified as Hkb ChIP-Seq targets (Figure 6A; Supplementary file 3), providing further evidence for the involvement of Hkb in intracellular trafficking.The initial difference in Hkb levels in the SG placode may lead to differential expression of these genes, which could contribute to normal invagination positioning.
In conclusion, we have uncovered a role for the Hkb transcription factor in regulating endoreplication and preventing abnormal cell cycle progression during epithelial tube formation.Our findings provide valuable insights into a critical mechanism for coordinating cell cycle regulation and morphogenesis during organ formation.

Fly stocks and genetics
The fly stocks used in this study are listed in Supplementary file 1.All the crosses were performed at 25 °C, except for Hkb expression using fkh-Gal4 and UAS-Hkb for the rescue experiment, which was performed at 29 °C for higher levels of transgene expression.

Immunostaining and imaging
Drosophila embryos were collected on grape juice agar plates at 25 °C.Embryos were dechorionated by incubating in 50% bleach for 3 min.For most samples, embryos were fixed in formaldehydesaturated heptane for 40 min and devitellinized using 80% ethanol.Following this, the embryos were stained with primary and secondary antibodies in PBSTB (1 X PBS, 0.2% bovine serum albumin, and 0.1% Triton X-100).For phalloidin and sqh-GFP signals, embryos were hand-devitellinized and stained with primary and secondary antibodies in PBTr (1 X PBS and 0.1% Triton X-100).The antibodies used in this study and their respective dilutions are listed in Supplementary file 2. After staining, embryos were mounted in Aqua-Poly/Mount (Polysciences, Inc) and imaged with Leica SP8 confocal microscope using 63 x, NA 1.4, and 40 x, NA 1.3 objectives.For horseradish peroxidase (HRP) staining, the VECTASTAIN ABC-HRP Kit, Peroxidase (PK-4000; Vector Laboratories) was used with biotinconjugated secondary antibodies.Whole embryo HRP images were acquired with a Leica DM2500 microscope using a 20x, 0.8 NA objective.
Cell segmentation, apical area quantification, and scatter plots SGs in early (pre-invagination; invagination depth, 0 µm) and late (during invagination; invagination depth, 5-10 µm) stage 11 of embryos were used.Confocal images of the SG were obtained from embryos immunostained for the Ecad (adherens junctions) and CrebA (SG cell nuclei) and used for cell segmentation.A maximum intensity projection was generated using the LasX program from three apical z-sections of confocal images of SG cells encompassing the adherens junction.Using the maximum intensity projection, cells were segmented using Ecad signals as a marker for each cell boundary using Imaris software (Andor).The apical area was calculated using Imaris and individual cells were color-coded based on the size of their apical areas.The frequency distribution of the apical area of the cells was analyzed using GraphPad Prism with the data exported from Imaris.Since the output data from Imaris for the apical area quantification is a sum of the area of both sides of the cell layer, we further divided the values by 2 to obtain the apical area of SG cells.
Scatter plots were generated using the X and Y coordinates for each SG cell, which were determined with respect to the A/P and D/V axes of the tissue using Imaris.The cell at the center of the SG placode was used as the origin point (X=0, Y=0).

Quantification of SG cell numbers
Confocal microscopy stacks for SGs with SG-specific nuclear markers (CrebA or Sage) were used for early stage 11 (pre-invagination) and stage 15+ embryos.3D-reconstructed images were generated using Imaris.The number of nuclei for each 3D-reconstructed SG was counted using cell ID numbers.
Quantification of SG lumen length and apical area of individual SG cells at stage 15 SG lumen length at stage 15 was measured for the secretory portion of the gland based on CrebA signals, which are exclusively expressed in the secretory cells at this stage.Confocal images immunolabeled with markers for Ecad and CrebA for stage 15 SGs were used.8-12 z-section images of the SG were merged to obtain a maximum projection image clearly showing half of the SG lumen and its apical surface.Segmentation of SG cells and quantification of apical areas of individual cells were performed using Imaris as described for segmentation of SG cells at stage 11.
For the lumen length quantification, maximum intensity projection images were imported into the ImageJ software (Fiji).The length of the SG lumen was measured along the line following the midpoint of the secretory portion of the tube.

Quantification of SG phenotypes at embryonic stages 12 and 15+
After performing HRP staining with CrebA, the SGs were manually categorized based on their phenotypes.At stage 12, WT SGs turn and migrate towards the posterior of the embryo after reaching the visceral mesoderm.SGs showing such normal behavior were categorized as 'normal,' while those SGs that reached the visceral mesoderm and migrated slightly were categorized as 'turned but short,' and those SGs that reached the visceral mesoderm but did not migrate posteriorly were categorized as 'not turned'.
For stage 15+ embryos, SGs that were comparable in shape, size, and position to WT SGs were categorized as 'normal;' SGs that had a rounded/ball-like morphology were categorized as 'very short/rounded;' SGs that were slightly elongated but not as long as WT SGs and mislocalized anteriorly were categorized as 'intermediate, mislocalized;' SGs that were slightly elongated but in the normal position were categorized as 'intermediate, normal position.'SGs that were as long as WT but mislocalized anteriorly were categorized as 'long, mislocalized'.

Analysis of modENCODE Hkb ChIP-Seq targets
The dataset was downloaded from the ENCODE Portal (https://www.encodeproject.org/).Total 1268 ChIP-Seq targets were analyzed using Database for Annotation, Visualization, and Integrated Discovery (DAVID; Dennis et al., 2003).

EdU labeling
To visualize SG cells in the S phase of the cell cycle or undergoing endoreplication, dechorionated embryos were incubated in n-octane (Thermo Scientific Chemicals: 325950010) for 3 min to permeabilize the vitelline membrane.Embryos were then washed five times in 1 x PBS in a microcentrifuge tube before being pulsed with 100 µM EdU (Thermo Fisher: C10637) for 30 min.Following EdU labeling, embryos were washed five times for 5 min each in PBSTB and incubated with azide-conjugated Alexa Fluor 488 for 30 min at room temperature.Embryos were further stained with CrebA and Crumbs antibodies to mark SG cell nuclei and apical cell boundaries, respectively.

Fluorescence in situ hybridization
Dechorionated Drosophila embryos were fixed in paraformaldehyde-heptane solution for 30 min, followed by devitellinization using methanol.Freshly fixed embryos were then labeled with digoxigenin (DIG)-labeled antisense probes following the standard procedure described in Knirr et al., 1999.After rehydration and post-fixation in 10% formaldehyde, embryos were pre-hybridized for 1 hr at 55 °C.mRNA probes were added to the embryos which were then incubated for 16 hr at 55 °C.DIG present on the synthesized mRNA probes was subsequently labeled with anti-DIG primary antibody (Enzo; ENZ-ABS302-0001; 1:1,000) and biotin-conjugated secondary antibody (Invitrogen; 1:500).To detect fluorescent signals, embryos were incubated with AB solution (PK-6100, Vectastain Elite ABC kit) followed by the tyramide signal amplification reaction (Cy3 fluorescent dye in amplification diluent; 1:50) (Perkin Elmer Life Sciences, NEL753001kt).To mark the SG and the apical membrane, the embryos were immunolabeled with antibodies for CrebA (SG nuclei) and Crb (apical membrane).
Primer sequences used for mRNA probe synthesis in this study are listed below.Quantification of in situ hybridization signals Stage 11 hkb mutant and WT SGs were used.A maximum intensity projection was generated using two z-sections of confocal images of SG cells.Z-sections were obtained from the same depth in all instances.Snapshots of these sections were imported into Fiji (NIH), and SG mRNA expression levels were measured by obtaining the mean gray value of the fluorescence intensity across the SG placode.SG placode-specific measurements were performed using SG-expressed CrebA signals.For each mRNA quantification, background subtraction was done using 10-15 cells in the epidermis in the lateral ectoderm region of parasegment 2 near the SG.Statistical analysis was performed using GraphPad Prism.

MatthewFigure 1 .
Figure 1.Generation of new huckebein (hkb) alleles and fluorescent knock-in lines reveals its function and tissue-specific localization during salivary gland (SG) morphogenesis.(A) Top cartoon diagram: Anterior region of stage 11 and 15 Drosophila embryos.SGs shown in yellow.Brown area, clustered apical constriction of SG cells during invagination.Black, invagination pit.Arrowheads, salivary duct.Bottom cartoon diagram: Lateral view of SG at stages 11 and 15.Orange circles, SG cell nuclei.Gray, SG lumen.(B) Top cartoon diagram: hkb transcript displayed with coding exon in Figure 1 continued on next page Figure supplement 1. Indels of the CRISPR/Cas9 huckebein (hkb) alleles and predicted protein sequences for each allele.

Figure
Figure supplement 5. huckebein (hkb) mutants show short salivary duct phenotypes with reduced cell numbers and cell intercalation defects.

Figure 2
Figure 2 continued on next page -mCh SG cells showed no DCP-1 signals (Figure 2H and N), except for a single cell at the anterior boundary of the SG placode in some stage 11 embryos (Arrowhead in Figure 2H).In contrast, SGs in hkb mutants and Hkb mut -mCh embryos displayed significant DCP-1 signals at stages 11 and 12 (Figure 2I-K, O and P and Figure 2-figure supplement 1A-C').DAPI staining revealed condensed and fragmented nuclei in some SG cells in hkb mutants (Figure 2Q and Q'), a hallmark of pyknosis

Figure
Figure supplement 3. huckebein (hkb) mutant salivary glands (SGs) have a smaller apical domain size with Rab11 mislocalized to the basolateral domain.
, as well as 5-Ethynyl-2'-deoxyuridine (EdU) labeling to specifically mark S phase or endocycling cells.Prior to invagination at early stage 11, all WT SG cells exhibited strong nuclear signals for E2f1 and cytoplasmic signals for CycB (Figure 5B-B'') and no EdU signals (Figure 5D), indicating G2 phase.During late stage 11 and stage 12, distal SG cells that had completed invagination showed reduced E2f1 signals and very low levels of CycB (Figure 5F-F''), with high EdU signals (Figure 5H and Figure 5-figure supplement 1A), consistent with a previous finding using BrdU staining (Chandrasekaran and Beckendorf, 2005).By stage 13, nuclear E2f1 signals were almost completely lost in all SG cells, accompanied by low levels of CycB (Figure 5J-J'') and high EdU signals (Figure 5L).These data indicate a distal-to-proximal transition to S phase.At late stage 13, distal SG cells began to show weak E2f1 (arrowheads in Figure 5J') and EdU signals (arrowheads in Figure 5L), and by stage 14, most SG cells had regained E2f1 signals (Figure 5N-N'') and lost EdU signals (Figure 5P) except for a few proximal cells (arrowheads in Figure 5N' and P), indicating a distal-to-proximal transition to G2 phase.During stages 15 and 16, almost all SG cells had accumulated E2f1 signals along with increased CycB expression (Figure 5R-R'') and lost EdU signals (Figure 5T).Interestingly, in some late-stage SGs, a few distal cells lacked E2f1 signals and showed the variable intensity of EdU signals (arrowheads in Figure 5R-R'' and T; arrowheads in Figure 5-figure supplement 1E), indicating re-entry into S phase and the onset of a potential second wave of endoreplication.Taken together, our data suggest a distal-to-proximal wave of endoreplication progression during normal SG morphogenesis.
figure supplement 1A-I).Similar to WT, most cells in early stage 11 hkb mutant SGs exhibited strong nuclear signals for E2f1 and cytoplasmic CycB signals, with little to no EdU signal (Figure 5C-C'' and E), except in dividing cells where CycB signals were distributed throughout the entire cell (arrowheads in Figure 5C''), which is consistent with the distribution of CycB during mitosis

Figure 5 .
Figure 5.The distal-to-proximal progression of the endoreplication is disrupted in the huckebein (hkb) mutant salivary gland (SG).(A) Schematic of the Fly-FUCCI system.(B-C'', F-G'', J-K'', N-O'', R-S'') SGs immunolabeled with GFP (for E2f1-GFP; green) and cytoplasmic cyclin B (CycB) (for CycB-RFP; magenta) at different stages.Red arrowheads in C'', CycB signals distributed throughout the dividing cells.Asterisk in F', absence of E2F transcription factor 1 (E2f1) signals in distal cells of stage 12 SG.Red arrowheads in J', weak E2f1 signals in the proximal SG cells.Red arrowheads in N' and R', little to no E2f1 signal in proximal (N') and distal (R') SG cells.(D-E, H-I, L-M, P-Q, T-U) 5-Ethynyl-2'-deoxyuridine (EdU)-labeled SGs at different developmental stages.Blue arrowhead in E, EdU-positive single SG cell.Asterisks in H, absence of EdU signals in proximal cells of late stage 11 SG.Blue arrowheads in L, P, and T, weak EdU signals in distal (L, T) and proximal (P) SG cells.Yellow dotted lines, SG boundary determined by SG-specific CrebA signals.Due to the proximity of the two SGs in hkb mutants, one or two SGs are shown depending on the orientation of the embryo.dis.denotes distal; prox.denotes proximal.© 2024, Matthew et al.Figure 5 was created using BioRender, and is published under a CC BY-NC-ND 4.0 license.Further reproductions must adhere to the terms of this license.

Figure 5
was created using BioRender, and is published under a CC BY-NC-ND 4.0 license.Further reproductions must adhere to the terms of this license.The online version of this article includes the following figure supplement(s) for figure5:

Figure supplement 1 .
Figure supplement 1.Expression levels of key cell cycle and cell death genes in wild-type (WT) and huckebein (hkb) mutant embryos.

Figure supplement 3 .
Figure supplement 3. Genetic inhibition of the function of key cell cycle genes is sufficient to suppress cell death and cell division in huckebein (hkb) mutants.

Figure supplement 4 .
Figure supplement 4. Inhibition of cell division or cell death partially rescues the salivary gland (SG) phenotypes of huckebein (hkb) mutants.

Figure 7 .
Figure 7.A model of endoreplication regulation by Huckebein (Hkb) during salivary gland (SG) morphogenesis.(A) Cartoon diagram showing the cell cycle status and progression of endoreplication during SG morphogenesis.Cells with green nuclei represent cells with E2F transcription factor (E2f1) signals (G phase).Cells with white nuclei represent cells with 5-Ethynyl-2'-deoxyuridine (EdU signals S phase).(B) Summary of the role of Hkb in cell cycle regulation in the SG.Hkb helps to inhibit cell division and cell death and promotes endoreplication progression through transcriptional inhibition of key cell cycle and pro-apoptotic genes.Cell death in hkb mutant SG may also be caused by DNA damage-induced cell death.Yellow bars represent cell cycle checkpoints.© 2024, Matthew et al.Figure 7 was created using BioRender, and is published under a CC BY-NC-ND 4.0 license.Further reproductions must adhere to the terms of this license.
Figure 7 was created using BioRender, and is published under a CC BY-NC-ND 4.0 license.Further reproductions must adhere to the terms of this license.