hnRNPH1 recruits PTBP2 and SRSF3 to modulate alternative splicing in germ cells

被引:42
|
作者
Feng, Shenglei [1 ]
Li, Jinmei [1 ]
Wen, Hui [1 ]
Liu, Kuan [1 ]
Gui, Yiqian [1 ]
Wen, Yujiao [1 ]
Wang, Xiaoli [1 ]
Yuan, Shuiqiao [1 ,2 ,3 ]
机构
[1] Huazhong Univ Sci & Technol, Inst Reprod Hlth, Tongji Med Coll, Wuhan 430030, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Lab Anim Ctr, Wuhan 430030, Hubei, Peoples R China
[3] Shenzhen Huazhong Univ Sci & Technol Res Inst, Shenzhen 518057, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
RNA; SPERMATOGENESIS; EXPRESSION; IDENTIFICATION; TRANSCRIPTOME; PROTEINS; ISOFORMS; REGION;
D O I
10.1038/s41467-022-31364-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Coordinated regulation of alternative splicing is essential for germ cell development. Here, the authors report that hnRNPH1 interacts with alternative splicing factors PTBP2 and SRSF3 in the germline to regulate pre-mRNA alternative splicing. Coordinated regulation of alternative pre-mRNA splicing is essential for germ cell development. However, the underlying molecular mechanism that controls alternative mRNA expression during germ cell development remains elusive. Herein, we show that hnRNPH1 is highly expressed in the reproductive system and recruits the PTBP2 and SRSF3 to modulate the alternative splicing in germ cells. Conditional knockout Hnrnph1 in spermatogenic cells causes many abnormal splicing events, thus affecting the genes related to meiosis and communication between germ cells and Sertoli cells. This is characterized by asynapsis of chromosomes and impairment of germ-Sertoli communications, which ultimately leads to male sterility. Markedly, Hnrnph1 germline-specific mutant female mice are also infertile, and Hnrnph1-deficient oocytes exhibit a similar defective synapsis and cell-cell junction as seen in Hnrnph1-deficient male germ cells. Collectively, our data support a molecular model wherein hnRNPH1 governs a network of alternative splicing events in germ cells via recruitment of PTBP2 and SRSF3.
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收藏
页数:19
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