Genetic basis for developmental homeostasis of germline stem cell niche number: a network of Tramtrack-Group nuclear BTB factors

PLoS One. 2012;7(11):e49958. doi: 10.1371/journal.pone.0049958. Epub 2012 Nov 21.

Abstract

The potential to produce new cells during adult life depends on the number of stem cell niches and the capacity of stem cells to divide, and is therefore under the control of programs ensuring developmental homeostasis. However, it remains generally unknown how the number of stem cell niches is controlled. In the insect ovary, each germline stem cell (GSC) niche is embedded in a functional unit called an ovariole. The number of ovarioles, and thus the number of GSC niches, varies widely among species. In Drosophila, morphogenesis of ovarioles starts in larvae with the formation of terminal filaments (TFs), each made of 8-10 cells that pile up and sort in stacks. TFs constitute organizers of individual germline stem cell niches during larval and early pupal development. In the Drosophila melanogaster subgroup, the number of ovarioles varies interspecifically from 8 to 20. Here we show that pipsqueak, Trithorax-like, batman and the bric-à-brac (bab) locus, all encoding nuclear BTB/POZ factors of the Tramtrack Group, are involved in limiting the number of ovarioles in D. melanogaster. At least two different processes are differentially perturbed by reducing the function of these genes. We found that when the bab dose is reduced, sorting of TF cells into TFs was affected such that each TF contains fewer cells and more TFs are formed. In contrast, psq mutants exhibited a greater number of TF cells per ovary, with a normal number of cells per TF, thereby leading to formation of more TFs per ovary than in the wild type. Our results indicate that two parallel genetic pathways under the control of a network of nuclear BTB factors are combined in order to negatively control the number of germline stem cell niches.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • DNA-Binding Proteins* / genetics
  • DNA-Binding Proteins* / metabolism
  • Drosophila Proteins* / genetics
  • Drosophila Proteins* / metabolism
  • Drosophila melanogaster / genetics
  • Drosophila melanogaster / growth & development
  • Female
  • Gene Dosage / genetics
  • Gene Expression Regulation, Developmental
  • Germ Cells / cytology
  • Germ Cells / growth & development
  • Homeostasis / genetics
  • Homeostasis / physiology
  • Morphogenesis
  • Nuclear Proteins* / genetics
  • Nuclear Proteins* / metabolism
  • Ovary / cytology
  • Ovary / growth & development
  • Stem Cell Niche / genetics*
  • Stem Cell Niche / physiology
  • Transcription Factors* / genetics
  • Transcription Factors* / metabolism

Substances

  • Bric-a-brac protein 1, Drosophila
  • DNA-Binding Proteins
  • Drosophila Proteins
  • Nuclear Proteins
  • Transcription Factors
  • Trl protein, Drosophila
  • lolal protein, Drosophila
  • psq protein, Drosophila

Grants and funding

This work was supported by National Centre for Scientific Research and Université de Versailles Saint-Quentin, and grants from Region Ilede-France (convention SESAME1655) and Association pour la Recherche sur le Cancer (ARC 4710). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.