Full Papers
The Function of argos in Regulating Cell Fate Decisions during Drosophila Eye and Wing Vein Development

https://doi.org/10.1006/dbio.1994.1197Get rights and content

Abstract

The Drosophila argos gene, which encodes a secreted protein with an EGF motif, is involved in several developmental processes regulating cell-cell interactions such as eye morphogenesis. Loss-of-function mutations in the argos gene cause an increase in the number of photoreceptor cells and cone cells, impaired retinal projections to the optic lobe, and the formation of extra veins. We show here that ubiquitously expressed argos product restored all these loss-of-function phenotypes. Overexpression of argos in the wild-type background resulted in the reduced number of photoreceptor cells, cone cells, and pigment cells, which are phenotypes opposite to those of the loss-of-function mutants. The argos gene is expressed in developing wing veins. Ubiquitous argos expression caused loss of veins in a dose-dependent manner. This phenotype was enhanced by the loss-of-function rhomboid mutation, implying the possibility that argos and rhomboid play key roles in a common pathway for normal wing vein formation. We propose that argos acts as an inhibitory signal for cellular differentiation in the developing eye and wing.

References (0)

Cited by (69)

  • Hexagonal patterning of the Drosophila eye

    2021, Developmental Biology
    Citation Excerpt :

    First, apoptosis removes numerous excess ICs to leave just nine about an ommatidium (six 2°s and three 3°s, Fig. 1A). Apoptosis is promoted by N, Wingless (Wg) and Jun N-terminal kinase (JNK) signaling activities and opposed by EGFR and Yorkie (Yrk) (Bushnell et al., 2018; Cagan and Ready, 1989b; Cordero et al., 2004; DeAngelis et al., 2020; Freeman, 1996; Miller and Cagan, 1998; Querenet et al., 2015; Sawamoto et al., 1994, 1998; Wolff and Ready, 1991; Yu et al., 2002). Except for Wg, these signals are similarly associated with cell death or survival in other tissues.

  • Programmed Cell Death and Caspase Functions During Neural Development

    2015, Current Topics in Developmental Biology
    Citation Excerpt :

    Furthermore, irreC-rst mislocalization is observed in Delta and Notch mutants (Gorski, Brachmann, Tanenbaum, & Cagan, 2000). Argos is a soluble antagonist of the Drosophila EGF receptor (dEGFR) (Freeman, Klambt, Goodman, & Rubin, 1992; Sawamoto et al., 1994; Schweitzer, Howes, Smith, Shilo, & Freeman, 1995). Overexpression of argos or dominant negative dEGFR induces excess apoptosis of lattice cells, indicating the survival signal for lattice cells acts through dEGFR/dRas1 (Freeman, 1996; Sawamoto et al., 1994).

  • Spatial and temporal organization of signaling pathways

    2014, Trends in Biochemical Sciences
    Citation Excerpt :

    One example of this is the interaction between Notch and EGFR signaling pathways in different cell types within the developing wing disc. Notch and EGFR pathways have an antagonistic relationship in the wing pouch, with EGFR promoting wing vein formation and Notch inhibiting it [6–12]. EGFR activity in the vein tissue stimulates expression of Delta [6], which activates Notch signaling in the neighboring intervein tissues.

  • Rabex-5 ubiquitin ligase activity restricts Ras signaling to establish pathway homeostasis in drosophila

    2010, Current Biology
    Citation Excerpt :

    Increased Ras signaling causes melanotic tumors [13], as seen upon loss of Rabex-5. Ras activity is required for wing vein specification and, in excess, causes ectopic veins [14, 15], as seen upon Rabex-5 reduction. Ras is also important in the eye.

View all citing articles on Scopus
View full text