Theodore, L. | Search bioRxiv

bioRxiv2026

Natural genetic variation spans all predicted Rh5/Rh6 expression phenotypes in Drosophila R8 photoreceptors

Standing genetic variation is immediately available to selection, but how broad a range of phenotypes it can produce remains unknown for many traits. Here we address this question using the mutually exclusive Rhodopsin 5 (Rh5) and Rhodopsin 6 (Rh6) expression pattern in Drosophila R8 photoreceptors, a neuronal differentiation readout that permits enumeration of a finite set of predicted qualitative phenotypic changes. Wild flies and wild-derived inbred lines from the Drosophila Genome Reference Panel 2 (DGRP2) showed extensive variation in Rh5/Rh6 expression, including shifts in the relative abundance of Rh5- and Rh6-expressing R8s, Rh5/Rh6 co-expression, and loss of Rh5 or Rh6. Among 205 DGRP2 lines, we observed examples spanning all eight predicted qualitative phenotype categories. We also identified causal coding and regulatory variants, including alleles of sevenless, Rh5 and Rh6, and an intronic deletion in melted. These results show that standing natural variation can span the full predicted range of qualitative phenotypes in this system.

genetics↗

bioRxiv2019

The Bric-a-Brac transcription factors are necessary for formation of functional germline stem cell niches through control of dpp expression in the Drosophila melanogaster ovary

Many studies have focused on the mechanisms of stem cell maintenance via their interaction with a particular niche or microenvironment in adult tissues, but how formation of a functional niche is initiated, including how stem cells within a niche are established, is less well understood. Adult Drosophila melanogaster ovary Germline Stem Cell (GSC) niches are comprised of somatic cells forming a stack called a Terminal Filament (TF) and underlying Cap Cells (CCs) and Escort Cells (ECs), which are in direct contact with GSCs. In the adult, the Engrailed (En) transcription factor is specifically expressed in niche cells where it directly controls expression of the decapentaplegic gene (dpp) encoding a member of the Bone Morphogenetic Protein (BMP) family of secreted signaling molecules, which are key factors for GSC maintenance. In late third instar larval ovaries, in response to BMP signaling from newly-formed niches, adjacent primordial germ cells become GSCs. The bric-a-brac paralogs (bab1 and bab2) encode BTB/POZ-domain containing transcription factors, that are also expressed in developing GSCs niches where they are required for TF formation. Here, we demonstrate that Bab1 and Bab2 display redundant cell autonomous function for TF morphogenesis and we identify a new function for these genes in GSC establishment. Moreover, we show that Bab proteins control dpp expression in otherwise correctly specified CCs, independently of En and its paralog Invected (Inv). In fact, our results also indicate that en/inv function in larval stages are neither essential for TF formation, nor GSC establishment. Finally, when bab2 was overexpressed in ovarian somatic cells outside of the niche, where en/inv were not expressed, ectopic BMP signaling activation was induced in adjacent germ cells of adult ovaries, which formed GSC-like tumors. Together, these results indicate that Bab transcription factors are positive regulators of BMP signaling for acquisition of GSC status.

developmental biology↗