| Literature DB >> 28552346 |
Lan-Tao Gou1, Jun-Yan Kang2, Peng Dai2, Xin Wang2, Feng Li2, Shuang Zhao2, Man Zhang3, Min-Min Hua4, Yi Lu5, Yong Zhu6, Zheng Li6, Hong Chen7, Li-Gang Wu2, Dangsheng Li8, Xiang-Dong Fu9, Jinsong Li10, Hui-Juan Shi11, Mo-Fang Liu12.
Abstract
Genetic studies have elucidated critical roles of Piwi proteins in germline development in animals, but whether Piwi is an actual disease gene in human infertility remains unknown. We report germline mutations in human Piwi (Hiwi) in patients with azoospermia that prevent its ubiquitination and degradation. By modeling such mutations in Piwi (Miwi) knockin mice, we demonstrate that the genetic defects are directly responsible for male infertility. Mechanistically, we show that MIWI binds the histone ubiquitin ligase RNF8 in a Piwi-interacting RNA (piRNA)-independent manner, and MIWI stabilization sequesters RNF8 in the cytoplasm of late spermatids. The resulting aberrant sperm show histone retention, abnormal morphology, and severely compromised activity, which can be functionally rescued via blocking RNF8-MIWI interaction in spermatids with an RNF8-N peptide. Collectively, our findings identify Piwi as a factor in human infertility and reveal its role in regulating the histone-to-protamine exchange during spermiogenesis.Entities:
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Year: 2017 PMID: 28552346 PMCID: PMC5985145 DOI: 10.1016/j.cell.2017.04.034
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582