4.4 Article

Regulation of meiotic progression by Sertoli-cell androgen signaling

期刊

MOLECULAR BIOLOGY OF THE CELL
卷 31, 期 25, 页码 2841-2862

出版社

AMER SOC CELL BIOLOGY
DOI: 10.1091/mbc.E20-05-0334

关键词

-

资金

  1. National Institutes of Health (NIH) [HD33816, 1R21HD090371-01A1, 1DP2HD091949-01, F30HD097961]
  2. Michigan Institute for Data Science (MIDAS) grant
  3. NIH [P30 CA034196]
  4. CTRB [5T32HD079342-04]
  5. MSTP [5T32GM007863-38]
  6. Open Philanthropy Grant [2019-199327 (5384)]
  7. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT [F30HD097961] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Androgen receptor (AR) signaling in Sertoli cells is known to be important for germ-cell progression through meiosis, but the extent to which androgens indirectly regulate specific meiotic stages is not known. Here, we combine synchronization of spermatogenesis, cytological analyses and single-cell RNAseq (scRNAseq) in the Sertoli-cell androgen receptor knockout (SCARKO) mutant and control mice, and demonstrate that SCARKO mutant spermatocytes exhibited normal expression and localization of key protein markers of meiotic prophase events, indicating that initiation of meiotic prophase is not androgen dependent. However, spermatocytes from SCARKO testes failed to acquire competence for the meiotic division phase. ScRNAseq analysis of wild-type and SCARKO mutant testes revealed a molecular transcriptomic block in an early meiotic prophase state (leptotene/zygotene) in mutant germ cells, and identified several misregulated genes in SCARKO Sertoli cells, many of which have been previously implicated in male infertility. Together, our coordinated cytological and scRNAseq analyses identified germ-cell intrinsic and extrinsic genes responsive to Sertoli-cell androgen signaling that promotes cellular states permissive for the meiotic division phase.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Neurosciences

Shared proteomic effects of cerebral atherosclerosis and Alzheimer's disease on the human brain

Aliza P. Wingo, Wen Fan, Duc M. Duong, Ekaterina S. Gerasimov, Eric B. Dammer, Yue Liu, Nadia Harerimana, Bartholomew White, Madhav Thambisetty, Juan C. Troncoso, Namhee Kim, Julie A. Schneider, Ihab M. Hajjar, James J. Lah, David A. Bennett, Nicholas T. Seyfried, Allan Levey, Thomas S. Wingo

NATURE NEUROSCIENCE (2020)

Article Genetics & Heredity

Genetic control of the human brain proteome

Chloe Robins, Yue Liu, Wen Fan, Duc M. Duong, Jacob Meigs, Nadia Harerimana, Ekaterina S. Gerasimov, Eric B. Dammer, David J. Cutler, Thomas G. Beach, Eric M. Reiman, Philip L. De Jager, David A. Bennett, James J. Lah, Aliza P. Wingo, Allan Levey, Nicholas T. Seyfried, Thomas S. Wingo

Summary: The study generated an online brain pQTL resource for 7,376 proteins by analyzing genetic and proteomic data from the dorsolateral prefrontal cortex of 330 older adults. The identified pQTLs tend to be non-synonymous variations, over-represented among brain disease-associated variants, and show good replication in an independent brain dataset. Comparison with brain eQTLs revealed that most pQTLs are also eQTLs, suggesting lower pQTL mapping power and greater evolutionary constraint on protein abundance.

AMERICAN JOURNAL OF HUMAN GENETICS (2021)

Article Genetics & Heredity

A Genetic Study of Cerebral Atherosclerosis Reveals Novel Associations with NTNG1 and CNOT3

Selina M. Vattathil, Yue Liu, Nadia Harerimana, Adriana Lori, Ekaterina S. Gerasimov, Thomas G. Beach, Eric M. Reiman, Philip L. De Jager, Julie A. Schneider, David A. Bennett, Nicholas T. Seyfried, Allan Levey, Aliza P. Wingo, Thomas S. Wingo

Summary: This study identified a novel genetic locus NTNG1 associated with cerebral atherosclerosis and confirmed two significant SNPs. The research also revealed that these SNPs may impact cerebral atherosclerosis by regulating brain protein expression of CNOT3.
Article Neurosciences

Genetic Evidence Supporting a Causal Role of Depression in Alzheimer's Disease

Nadia Harerimana, Yue Liu, Ekaterina S. Gerasimov, Duc Duong, Thomas G. Beach, Eric M. Reiman, Julie A. Schneider, Patricia Boyle, Adriana Lori, David A. Bennett, James J. Lah, Allan Levey, Nicholas T. Seyfried, Thomas S. Wingo, Aliza P. Wingo

Summary: This study found a genetic correlation between depression and Alzheimer's disease (AD), suggesting a shared genetic basis. Depression was found to have a causal role in AD, potentially driven by specific brain transcripts and proteins. The findings highlight the importance of understanding the relationship between depression and AD.

BIOLOGICAL PSYCHIATRY (2022)

暂无数据