TY - JOUR
T1 - Tip60 complex promotes expression of a differentiation factor to regulate germline differentiation in female Drosophila
AU - McCarthy, Alicia
AU - Deiulio, Aron
AU - Martin, Elliot Todd
AU - Upadhyay, Maitreyi
AU - Rangan, Prashanth
N1 - Publisher Copyright:
© 2018 McCarthy et al. This article is distributed by The American Society for Cell Biology under license from the author(s).
PY - 2018/11/26
Y1 - 2018/11/26
N2 - Germline stem cells (GSCs) self-renew and differentiate to sustain a continuous production of gametes. In the female Drosophila germ line, two differentiation factors, bag of marbles (bam) and benign gonial cell neoplasm (bgcn), work in concert in the stem cell daughter to promote the generation of eggs. In GSCs, bam transcription is repressed by signaling from the niche and is activated in stem cell daughters. In contrast, bgcn is transcribed in both the GSCs and stem cell daughters, but little is known about how bgcn is transcriptionally modulated. Here we find that the conserved protein Nipped-A acts through the Tat interactive protein 60-kDa (Tip60) histone acetyl transferase complex in the germ line to promote GSC daughter differentiation. We find that Nipped-A is required for efficient exit from the gap phase 2 (G2) of cell cycle of the GSC daughter and for expression of a differentiation factor, bgcn. Loss of Nipped-A results in accumulation of GSC daughters. Forced expression of bgcn in Nipped-A germline-depleted ovaries rescues this differentiation defect. Together, our results indicate that Tip60 complex coordinates cell cycle progression and expression of bgcn to help drive GSC daughters toward a differentiation program.
AB - Germline stem cells (GSCs) self-renew and differentiate to sustain a continuous production of gametes. In the female Drosophila germ line, two differentiation factors, bag of marbles (bam) and benign gonial cell neoplasm (bgcn), work in concert in the stem cell daughter to promote the generation of eggs. In GSCs, bam transcription is repressed by signaling from the niche and is activated in stem cell daughters. In contrast, bgcn is transcribed in both the GSCs and stem cell daughters, but little is known about how bgcn is transcriptionally modulated. Here we find that the conserved protein Nipped-A acts through the Tat interactive protein 60-kDa (Tip60) histone acetyl transferase complex in the germ line to promote GSC daughter differentiation. We find that Nipped-A is required for efficient exit from the gap phase 2 (G2) of cell cycle of the GSC daughter and for expression of a differentiation factor, bgcn. Loss of Nipped-A results in accumulation of GSC daughters. Forced expression of bgcn in Nipped-A germline-depleted ovaries rescues this differentiation defect. Together, our results indicate that Tip60 complex coordinates cell cycle progression and expression of bgcn to help drive GSC daughters toward a differentiation program.
UR - http://www.scopus.com/inward/record.url?scp=85057125043&partnerID=8YFLogxK
U2 - 10.1091/mbc.e18-06-0385
DO - 10.1091/mbc.e18-06-0385
M3 - Article
C2 - 30230973
AN - SCOPUS:85057125043
SN - 1059-1524
VL - 29
SP - 2933
EP - 2945
JO - Molecular Biology of the Cell
JF - Molecular Biology of the Cell
IS - 24
ER -