TY - JOUR
T1 - Nanos downregulates transcription and modulates CTD phosphorylation in the soma of early Drosophila embryos
AU - Deshpande, Girish
AU - Calhoun, Gretchen
AU - Jinks, Timothy M.
AU - Polydorides, Alexandros D.
AU - Schedl, Paul
N1 - Funding Information:
We thank Gary Struhl, Paul Macdonald, Paul Lasko and Arno Greenleaf for antibodies, Claude Desplan, Liz Gavis, Judith Lengyel, and Robin Wharton for fly stocks. We would like to thank Trudi Schupbach, Eric Wieschaus, Liz Gavis and Daryl Gohl for advice. We also thank Radhika Mohan for help in preparing the manuscript. This work was supported by a grant from the N.I.H. (P.S.).
PY - 2005/5
Y1 - 2005/5
N2 - nanos (nos) specifies posterior development in the Drosophila embryo by repressing the translation of maternal hb mRNA. In addition to this somatic function, nos is required in the germline progenitors, the pole cells, to establish transcriptional quiescence. We have previously reported that nos is required to keep the Sex-lethal establishment promoter, Sxl-Pe, off in the germline of both sexes. We show here that nos also functions to repress Sxl-Pe activity in the surrounding soma. Sxl-Pe is inappropriately activated in the soma of male embryos from nos mothers, while Sxl-Pe can be repressed in female embryos by ectopic Nos protein. nos appears to play a global role in repressing transcription in the soma as the effects of nos on promoter activity are correlated with changes in the phosphorylation status of the carboxy terminal domain (CTD) repeats of the large RNA polymerase II subunit. Finally, we present evidence indicating that the suppression of transcription in the soma by Nos protein is important for normal embryonic development.
AB - nanos (nos) specifies posterior development in the Drosophila embryo by repressing the translation of maternal hb mRNA. In addition to this somatic function, nos is required in the germline progenitors, the pole cells, to establish transcriptional quiescence. We have previously reported that nos is required to keep the Sex-lethal establishment promoter, Sxl-Pe, off in the germline of both sexes. We show here that nos also functions to repress Sxl-Pe activity in the surrounding soma. Sxl-Pe is inappropriately activated in the soma of male embryos from nos mothers, while Sxl-Pe can be repressed in female embryos by ectopic Nos protein. nos appears to play a global role in repressing transcription in the soma as the effects of nos on promoter activity are correlated with changes in the phosphorylation status of the carboxy terminal domain (CTD) repeats of the large RNA polymerase II subunit. Finally, we present evidence indicating that the suppression of transcription in the soma by Nos protein is important for normal embryonic development.
KW - C-terminal domain (CTD)
KW - CTD phosphorylation
KW - Sex-lethal
KW - Transcriptional repression
KW - nanos
UR - http://www.scopus.com/inward/record.url?scp=16244371716&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=16244371716&partnerID=8YFLogxK
U2 - 10.1016/j.mod.2004.12.009
DO - 10.1016/j.mod.2004.12.009
M3 - Article
C2 - 15817222
AN - SCOPUS:16244371716
SN - 0925-4773
VL - 122
SP - 645
EP - 657
JO - Mechanisms of Development
JF - Mechanisms of Development
IS - 5
ER -