Unique Epigenetic Programming Distinguishes Regenerative Spermatogonial Stem Cells in The Developing Mouse Testis
Year: 2020
Type: article
Abstract: Spermatogonial stem cells (SSCs) both self-renew and give rise to progenitors that initiate spermatogenic differentiation in the mammalian testis. Questions remain regarding the extent to which the SSC and progenitor states are functionally distinct. Here we provide the first multiparametric integrative analysis of mammalian germ cell epigenomes comparable with that done for >100 somatic cell types by the ENCODE Project. Differentially expressed genes distinguishing SSC- and progenitor-enriched spermatogonia showed distinct histone modification patterns, particularly for H3K27ac and H3K27me3. Motif analysis predicted transcription factors that may regulate spermatogonial subtype-specific fate, and immunohistochemistry and gene-specific chromatin immunoprecipitation analyses confirmed subtype-specific differences in target gene binding of a subset of these factors. Taken together, these results show that SSCs and progenitors display distinct epigenetic profiling consistent with these spermatogonial subtypes being differentially programmed to either self-renew and maintain regenerative capacity as SSCs or lose regenerative capacity and initiate lineage commitment as progenitors.
Source: iScience
Language: English
Subfield: Reproductive Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $3,000
Awards: Control of Spermatogonial Stem Cell Fate Decisions by HLH Factors, Center for Male Reproductive Epigenomics, Mechanisms of stem cell specification in the male germline, Epimutations in Offspring Produced by Assisted Reproductive Technologies (ART), The role of retinoid exposure in specification of the foundational SSC pool, RCMI Center for Interdiscplinary Health Research CIHR, Origin and functional significance of the spermatogonial stem cell transcriptome barcode
OpenAlex ID: W3088307769
