α-Crystalline Domains and Intrinsically Disordered Regions Can Work in Parallel to Induce Accumulation of MBD6 at Chromocenters in Arabidopsis thaliana

Proteins are localized and concentrated at cellular and genomic locations for specific and efficient functions. Efforts to understand protein accumulation in eukaryotic organisms have primarily focused on multivalent interactions between intrinsically disordered regions (IDRs) as mediators of protein condensation. We previously showed that α-crystalline domain (ACD) proteins 15 (ACD15) and 21 (ACD21) were required for multimerization and the accumulation of gene-silencing methyl-CpG-binding domain protein 6 (MBD6) at chromocenters in Arabidopsis thaliana. Here, we demonstrate that ACDs and IDRs can act as parallel mechanisms, facilitating higher-order MBD6 assemblies. Using human IDRs known to be important for protein accumulation, we replicated and enhanced the accumulation of MBD6 at chromocenters. In addition, IDRs fused to MBD6 could substitute for ACD function and partially reconstitute the MBD6 gene-silencing function. However, the accumulation of MBD6 by IDRs still required ACD15 and ACD21 for full effect. These results establish that ACD-mediated protein accumulation is a mechanism that can function similarly to and together with IDR-mediated mechanisms.


Introduction
The efficient accumulation of proteins at the appropriate density and cellular location is critical to the function of many cellular pathways.Recent discoveries of phase-separated compartments in plant and animal nuclei, formed by density-dependent protein-protein interactions, highlight the link between protein accumulation and function [1][2][3][4][5].These supramolecular assemblies can be formed through multivalent interactions between the intrinsically disordered regions (IDRs) of proteins which are thought to function similarly to polymer-polymer interactions [5,6].In addition, IDRs often contain small regions called short linear motifs (SLiMs) that interact with the structured domains of other proteins to facilitate protein complex formation [7][8][9][10].
The MBD5/6 complex also contains the J-domain containing protein SILENZIO (SLN), which interacts with the chaperone protein HSP70 [11,14].Consistent with the known roles of sHSPs, ACD15 and ACD21 specifically bridge the interaction between MBD5/6 and SLN while mediating the accumulation of MBD5/6 [16].The silenzio, mbd5 mbd6, acd15, and acd21 mutants all have similar gene-silencing mutant defects, showing upregulation of the same collection of DNA-methylated genes and transposons [11].Fluorescence Recovery After Photobleaching (FRAP) experiments also showed that all of the MBD5/6 complex members are highly mobile when forming nuclear foci at chromocenters [11].However, the loss of SLN led to a significant decrease in MBD5/6 complex accumulation at the chromocenters and a decrease in mobility [11].These data suggest a model in which the multimerization and high-level accumulation of MBD5/6 at meCG sites are uniquely necessary aspects of their gene-silencing functions.However, gene-silencing by MBD5/6 and the novel, ACD-mediated accumulation mechanism are still not fully understood.
Because of the similarity between IDR and ACD15/21-mediated protein oligomerization, we sought to compare these mechanisms in the context of the MBD5/6 complex.Using MBD6 chromocenter localization as a measure of protein accumulation, we created chimeric MBD6 proteins containing human or plant IDRs and showed that they could synthetically hyper-accumulate MBD6 at the chromocenters [23,24].We then removed ACD15 and ACD21 or the MBD6 StkyC domain required for interaction with ACD15 and ACD21, leading to an inability of the MBD6-IDR chimeric proteins to hyper-accumulate at chromocenters, with only the strongest IDRs maintaining nuclear foci.However, the MBD6-IDR constructs that did maintain nuclear foci without ACD15 and ACD21 also retained some gene-silencing capacities.These results suggest that IDRs and ACD proteins act as parallel mechanisms to mediate protein accumulation and further support protein accumulation as an important aspect of the MBD5/6 complex's gene-silencing mechanism.

Human IDRs Can Stimulate the Accumulation of MBD6 Together with ACD15 and ACD21
MBD6 contains an IDR region between its MBD and StkyC domains, which is dispensable for function and protein accumulation in vivo [11].To determine if IDRs that are known to induce strong multimerization could contribute to MBD6 protein accumulation, we replaced the natural IDR of MBD6 (amino acids 149-167) with the amino acid sequence of two human IDRs: the hinge domain of HP1α (amino acids 70-117) and the second IDR region of MeCP2 (amino acids 167-486) (Figure 1A) [25,26].These IDRs vary in both the size and number of charged residues, but both IDRs induce strong multimerization in human and mouse cells, leading to the establishment of protein accumulation in chromatin (Figure S1A) [25][26][27][28].To control the amount of protein produced and avoid overexpression artifacts, MBD6-IDR chimeric proteins were expressed using the endogenous MBD6 promoter and contained C-terminal RFP tags for live cell imaging.To further confirm the combinatorial effect of IDR-and ACD-mediated accumulation on MBD6, we expressed HP1α and MeCP2 MBD6 chimeric proteins lacking the StkyC domain that is needed for the interaction of MBD6 with ACD15 (MBD6 HP1α-StkyC and MBD6 MeCP2-StkyC ) and compared these constructs with MBD6 HP1α and MBD6 MeCP2 in the mbd5 mbd6 mutant background (Figure 2A) [11].MBD6 HP1α and MBD6 MeCP2 again demonstrated a greatly increased number of nuclear foci as compared to wild-type MBD6.However, MBD6 HP1α-StkyC was unable to create nuclear foci, while the number of MBD6 MeCP2-StkyC foci significantly decreased as compared to MBD6 MeCP2 (Figure 2B,C).These nuclear phenotypes were further characterized by plotting the nuclear distribution of the RFP signal for the MBD6-IDR fusion constructs across root nuclei, which again highlighted the dramatic difference between MBD6 HP1α and MBD6 HP1α-StkyC , while the difference between MBD6 MeCP2 and MBD6 MeCP2-StkyC was less pronounced (Figure S2A-D).We also verified the decrease in chromocenter localization by staining for DNA using 4′,6-diamidino-2-phenylindole (DAPI), which confirmed that MBD6 HP1α overlaps with chromocenters while MBD6 HP1α-StkyC does not (Figure S2E).
These results demonstrate that IDRs can synthetically induce MBD6 to hyperaccumulate at chromocenters, with the IDRs of MeCP2 and H1.1 substantially substituting for the roles of ACD15 and ACD21 as mediators of MBD6 accumulation.This suggests that the mechanisms by which α-crystalline domains and intrinsically disordered regions accumulate proteins share similarities, leading to parallel phenotypic outcomes.

IDR Accumulation of MBD6 Is Associated with Gene Silencing
We showed previously that MBD6 chromocenter accumulation correlates with gene silencing by the MBD5/6 complex, wherein the losses of ACD15 and ACD21 lead to an inability of the MBD5/6 complex to accumulate or silence genes and TEs [11].We therefore hypothesized that MBD6-IDR chimeric proteins might replicate the gene-silencing function of MBD6 if MBD6-IDR proteins can sufficiently substitute for the role of ACD15 and Wild-type MBD6 consistently forms nuclear foci in root cells, localizing to chromocenters, and this process depends on binding to methylated DNA through the MBD domain and on interaction with ACD15/ACD21 to accumulate MBD6 and its complex members [11,14].Remarkably, we found that the replacement of the natural IDR of MBD6 with the IDRs of HP1α (MBD6 HP1α ) or MeCP2 (MBD6 MeCP2 ) greatly increased MBD6 chromocenter localization as compared to wild-type MBD6, as quantified by the number of nuclear foci visualized in the root cells (Figure 1BC and Figure S1B).However, when the MBD6-IDR constructs were expressed in acd15 acd21 mutant plants, the increase in chromocenter localization was greatly diminished, with MBD6 HP1α showing a complete lack of nuclear foci and MBD6 MeCP2 showing a reduced number of nuclear foci (Figure 1B,C).The IDR of MeCP2 is over six times the size of the HP1α IDR, which is likely to provide more opportunities for multivalent interactions and the multimerization of complexes containing MBD6 MeCP2 proteins, possibly explaining its ability to create more foci than MBD6 HP1α .Notably, the number of MBD6 MeCP2 foci formed in acd15 acd21 mutant plants was roughly similar to the number of foci formed by wild-type MBD6, suggesting that an IDR can replace the role of ACD15 and ACD21 in MBD6 chromocenter accumulation (Figure 1C).
Because the two tested IDRs were of human origin, we also sought to test whether an endogenous plant IDR, not related to the MBD5/6 complex, could also drive the accumulation of MBD6.Therefore, we tested whether the IDR from the Arabidopsis linker histone H1.1 could also induce the accumulation of MBD6 at chromocenters and substitute for the function of ACD15 and ACD21.The C-terminal IDR of H1.1 was recently shown to be important in mediating H1.1 accumulation and forming phase-separated condensates at chromocenters similar to MBD6 [29].Like the human IDRs, we again swapped the natural IDR of MBD6 with the amino acid sequence of the C-terminal IDR of H1.1 (amino acid 130-274), which is three times the size of the HP1α IDR (Figure S1A).Similar to the human IDR fusion constructs, MBD6 H1.1 hyper-localized to chromocenters in the wild-type cells, forming nuclear foci with almost no diffuse signal in the nucleoplasm (Figure S1B,C).In addition, like MBD6 MeCP2 , MBD6 H1.1 retained nuclear foci formation in the acd15 acd21 mutant background, demonstrating that the H1.1 IDR could also substitute for the role of ACD15 and ACD21 in driving the accumulation of MBD6 at the chromocenters (Figure S1C).To control for the possibility that the increase in foci could be caused by excess protein, we also measured the RFP signal of individual wild-type nuclei from plants expressing MBD6, MBD6 HP1α , MBD6 MeCP2 , and MBD6 H1.1 .We found no significant differences between nuclear intensities, suggesting that the foci trends of MBD6-IDR constructs are not caused by differences in the amount of MBD6 in these nuclei (Figure S1D).
To further confirm the combinatorial effect of IDR-and ACD-mediated accumulation on MBD6, we expressed HP1α and MeCP2 MBD6 chimeric proteins lacking the StkyC domain that is needed for the interaction of MBD6 with ACD15 (MBD6 HP1α-StkyC and MBD6 MeCP2-StkyC ) and compared these constructs with MBD6 HP1α and MBD6 MeCP2 in the mbd5 mbd6 mutant background (Figure 2A) [11].MBD6 HP1α and MBD6 MeCP2 again demonstrated a greatly increased number of nuclear foci as compared to wild-type MBD6.However, MBD6 HP1α-StkyC was unable to create nuclear foci, while the number of MBD6 MeCP2-StkyC foci significantly decreased as compared to MBD6 MeCP2 (Figure 2B,C).These nuclear phenotypes were further characterized by plotting the nuclear distribution of the RFP signal for the MBD6-IDR fusion constructs across root nuclei, which again highlighted the dramatic difference between MBD6 HP1α and MBD6 HP1α-StkyC , while the difference between MBD6 MeCP2 and MBD6 MeCP2-StkyC was less pronounced (Figure S2A-D).We also verified the decrease in chromocenter localization by staining for DNA using 4 ′ ,6-diamidino-2-phenylindole (DAPI), which confirmed that MBD6 HP1α overlaps with chromocenters while MBD6 HP1α-StkyC does not (Figure S2E).
These results demonstrate that IDRs can synthetically induce MBD6 to hyperaccumulate at chromocenters, with the IDRs of MeCP2 and H1.1 substantially substituting for the roles of ACD15 and ACD21 as mediators of MBD6 accumulation.This suggests that the mechanisms by which α-crystalline domains and intrinsically disordered regions accumulate proteins share similarities, leading to parallel phenotypic outcomes.

IDR Accumulation of MBD6 Is Associated with Gene Silencing
We showed previously that MBD6 chromocenter accumulation correlates with gene silencing by the MBD5/6 complex, wherein the losses of ACD15 and ACD21 lead to an inability of the MBD5/6 complex to accumulate or silence genes and TEs [11].We therefore hypothesized that MBD6-IDR chimeric proteins might replicate the gene-silencing function of MBD6 if MBD6-IDR proteins can sufficiently substitute for the role of ACD15 and ACD21 in accumulating MBD6 at methylated sites (Figure 1B,C and Figure 2B,C).FWA is a promoter-methylated and silenced target of the MBD5/6 complex, which becomes derepressed in mbd5 mbd6 mutant plants, a phenotype that can be complemented upon the expression of wild-type MBD6-RFP [11,14].We therefore utilized FWA expression to measure the ability of MBD6-IDR fusion proteins to complement the gene-silencing function of MBD6 in mbd5 mbd6 mutant plants.
Using reverse transcription with quantitative PCR (RT-qPCR) from the RNA of flower buds, we found that MBD6 HP1α and MBD6 MeCP2 were able to significantly reduce the expression of FWA in mbd5 mbd6 plants (Figure 2D).However, MBD6 HP1α-StkyC , which was unable to form nuclear foci, led to no reduction in the FWA expression, showing that its silencing function was abolished (Figure 2B-D).On the other hand, MBD6 MeCP2-StkyC , which retained the ability to form nuclear foci, was able to significantly reduce FWA expression (Figure 2B-D).These gene expression results correlate with foci formation data, suggesting that gene silencing by MBD6 is at least in part dictated by efficient accumulation at methylated sites regardless of whether that accumulation is induced by ACD15/ACD21 or by IDRs.
silencing function was abolished (Figure 2B-D).On the other hand, MBD6 MeCP2-StkyC , which retained the ability to form nuclear foci, was able to significantly reduce FWA expression (Figure 2B-D).These gene expression results correlate with foci formation data, suggesting that gene silencing by MBD6 is at least in part dictated by efficient accumulation at methylated sites regardless of whether that accumulation is induced by ACD15/ACD21 or by IDRs.

Conclusions
Our results demonstrate that IDRs can synthetically drive the accumulation of MBD6 to chromocenters additively with ACD15 and ACD21, and that, surprisingly, they can overcome the need for ACD15 and ACD21 in some cases.The IDRs of HP1α, MeCP2, and H1.1 are all naturally required for those respective proteins to accumulate and form phase-separated compartments in cells [25,26,29].When added to MBD6, these IDRs mimicked the function of ACD15 and ACD21, likely acting as sites for protein-protein interactions between MBD6 proteins.The accumulation of MBD6 at chromocenters thus can be determined by the ability of MBD6 to form supramolecular assemblies, whether driven by ACDs or by IDRs (Figure 3.These results also suggest that the phase separation models proposed for HP1α, MeCP2, and H1.1 are likely operative in these MBD6-IDR chimeric proteins.Still, it is remarkable that the IDRs from human HP1α and MeCP2, both related to heterochromatin formation and gene silencing in humans, function in the context of plant heterochromatin.This suggests that IDRs may retain protein accumulation functions regardless of the organism in which they are utilized.

Plant Materials and Growth Conditions
All plants used in this study were in the Columbia-0 ecotype (Col-0).The plants were grown on soil in a greenhouse under long-day conditions (16h light/8h dark).The plants grown for microscopy were plated on 1/2xMS plates in growth rooms at room temperature (~25 °C), with 16h of light and 8h of dark.
The following mutant lines were previously described: mbd5 mbd6 T-DNA double mutant composed of mbd5 T-DNA line SAILseq_750_A09.1 and mbd6 T-DNA line SALK_043927.The acd15 acd21 mutant plant line was created using CRISPR-Cas9 editing as described previously [11].

Generation of Transgenic Lines
Transgenic plants expressing fluorescently tagged proteins were created using the pGWB553 destination vector obtained from Addgene.Specifically, the MBD6 promoter and coding sequences were PCR-amplified from genomic DNA and cloned into pENTR/D-TOPO vectors.These coding sequences were then inserted into the final destination vector (pGWB553) using the Gateway LR Clonase II Enzyme mix (Catalog number: 11791020, ThermoFisher, Los Angeles, CA, USA).These destination vectors were electro- Our results also further highlight the importance of protein accumulation for gene silencing by the MBD5/6 complex.Interestingly, MeCP2 can maintain some level of genesilencing function even without the StkyC domain.This suggests that protein accumulation of MBD6 alone can silence genes in Arabidopsis to a certain extent.However, because MBD6 MeCP2 and MBD6 MeCP2-StkyC silence FWA equally but not fully, this suggests that IDRs are not able to fully recapitulate the gene-silencing roles of ACD15 and ACD21 in the MBD5/6 complex.We suggest the possibility that a specific amount or quality of the accumulation is needed for gene silencing to happen efficiently.The additive nature of MBD6 accumulation via both ACDs and IDRs also emphasizes that the IDRand ACD-mediated protein accumulations are likely mechanistically related and can work simultaneously in the same complex.
It is important to highlight the primary use of an ACD-mediated mechanism to accumulate the MBD5/6 complex.We hypothesize that plants may have needed an efficient, organized, and regulated mechanism for protein accumulation and thus coopted small heat-shock proteins for this purpose.These findings are consistent with many early studies showing that sHSPs from different organisms form dynamic oligomeric complexes [16,17,22] and with more recent studies showing that some sHSPs are linked to the formation and regulation of phase separation events created by proteins utilizing IDRs for accumulation [30][31][32].Finally, our results further confirm and highlight that the multimerization and hyperaccumulation of MBD6 at DNA-methylated sites in heterochromatin are critical aspects of its gene-silencing function.

Plant Materials and Growth Conditions
All plants used in this study were in the Columbia-0 ecotype (Col-0).The plants were grown on soil in a greenhouse under long-day conditions (16h light/8h dark).The plants grown for microscopy were plated on 1/2xMS plates in growth rooms at room temperature (~25 • C), with 16h of light and 8h of dark.
The following mutant lines were previously described: mbd5 mbd6 T-DNA double mutant composed of mbd5 T-DNA line SAILseq_750_A09.1 and mbd6 T-DNA line SALK_043927.The acd15 acd21 mutant plant line was created using CRISPR-Cas9 editing as described previously [11].

Generation of Transgenic Lines
Transgenic plants expressing fluorescently tagged proteins were created using the pGWB553 destination vector obtained from Addgene.Specifically, the MBD6 promoter and coding sequences were PCR-amplified from genomic DNA and cloned into pENTR/D-TOPO vectors.These coding sequences were then inserted into the final destination vector (pGWB553) using the Gateway LR Clonase II Enzyme mix (Catalog number: 11791020, ThermoFisher, Los Angeles, CA, USA).These destination vectors were electroporated into AGL0 agrobacterium and transformed into Col0 (wild-type), mbd5 mbd6 (SALK_043927), and acd15 acd21 plants.The positive selection of transgenic plants was done on ½ MS agar plates with hygromycin B after 5 days in the dark at 4 • C, 8 h in the light at room temperature, and another 5 days in the dark at room temperature.All protein expression constructs in this paper are RFP tagged.

Confocal Microscopy
All confocal microscopy experiments were performed using the Zeiss, LSM 980 confocal microscope, Jena, Germany.Unless otherwise stated, all experiments were performed using a 40× magnification water objective lens.
Live plant samples were prepared for microscopy as follows: Two-week-old seedlings were grown on ½ MS plates at room temperature, ~25 • C, and transferred onto 1mm-thick glass slides (Fisherscientific, Los Angeles, CA, USA, Cat No. 12-550-08) containing deionized water (room temperature).The seedlings were oriented such that the roots were on the middle of the slide while leaves extended from the top of the slides.On top of the plant were placed #1.5 coverslips (Fisherscientific, Cat No. 12-544-EP).

Quantification of Foci Counts and Nuclear RFP Signal Distributions
All foci counts and nuclear distribution plots were quantified using ImageJ, image analysis software (https://imagej.net/(accessed on 22 August 2024)).
The nuclear intensities were measured using Zeiss, Zen Blue software (version 3.10).The nuclei were circled using the same diameter across the nuclei (8 µM), and the intensities were measured using the "measure" program of the Zeiss software (https://www.zeiss.com/microscopy/en/products/software/zeiss-zen.html(accessed on 22 August 2024)).These intensities were then plotted and compared using GraphPad Prism software (https: //www.graphpad.com/(accessed on 22 August 2024)).
A plot profile macro was used to obtain measurements of the RFP intensity of MBD6-IDR constructs across the nuclei for Supplemental Figure S2.The RFP intensity of each

Epigenomes 2024, 8 , 10 Figure 3 .
Figure 3. Model of MBD6 accumulation at methylated sites through endogenous and synthetic mechanisms (IDRs).The DNA methylation-binding protein, MBD6, can be synthetically hyper-accumulated using IDRs.However, ACD15 and ACD21 also control protein accumulation and can work together with these IDRs to maintain efficient MBD6 localization.Therefore, both mechanisms can functionally drive MBD6 accumulation.Made using BioRender.

Figure 3 .
Figure 3. Model of MBD6 accumulation at methylated sites through endogenous and synthetic mechanisms (IDRs).The DNA methylation-binding protein, MBD6, can be synthetically hyperaccumulated using IDRs.However, ACD15 and ACD21 also control protein accumulation and can work together with these IDRs to maintain efficient MBD6 localization.Therefore, both mechanisms can functionally drive MBD6 accumulation.Made using BioRender.