Abstract:
:Spermatogenesis is a complex process that requires coordinated proliferation and differentiation of male germ cells. The molecular events that dictate this process are largely unknown, but are likely to involve highly regulated transcriptional control. In this study, we investigate the contribution of chromatin associated Sin3A in mouse germ cell lineage development. Genetic inactivation of Sin3A in the male germline leads to sterility that results from the early and penetrant apoptotic death observed in Sin3A-deleted germ cells, coincident with the reentry in mitosis. Sin3A-deleted testes exhibit a Sertoli-cell only phenotype, consistent with the absolute requirement for Sin3A in germ cells' development and/or viability. Interestingly, transcripts analysis revealed that the expression program of Sertoli cells is altered upon inactivation of Sin3A in germ cells. These studies identified a central role for the mammalian Sin3-HDAC complex in the germ cell lineage, and point to an exquisite transcriptional crosstalk between germ cells and their niche to support fertility in mammals.
journal_name
Dev Bioljournal_title
Developmental biologyauthors
Pellegrino J,Castrillon DH,David Gdoi
10.1016/j.ydbio.2012.07.006subject
Has Abstractpub_date
2012-09-15 00:00:00pages
349-55issue
2eissn
0012-1606issn
1095-564Xpii
S0012-1606(12)00377-6journal_volume
369pub_type
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