Pachytene piRNAs instruct massive mRNA elimination during late spermiogenesis

Lan‐Tao Gou(Shanghai Institutes for Biological Sciences), Peng Dai(Shanghai Institutes for Biological Sciences), Jian-Hua Yang(Sun Yat-sen University), Yuanchao Xue(University of California San Diego), Yun-Ping Hu(Shanghai Institutes for Biological Sciences), Yu Zhou(University of California San Diego), Jun-Yan Kang(Shanghai Institutes for Biological Sciences), Xin Wang(Chinese Academy of Sciences), Hairi Li(University of California San Diego), Min-Min Hua(Shanghai Institutes for Biological Sciences), Shuang Zhao(Chinese Academy of Sciences), Si-Da Hu(Chinese Academy of Sciences), Li-Gang Wu(Shanghai Institutes for Biological Sciences), Hui-Juan Shi(Shanghai Institute of Planned Parenthood Research), Yong Li(University of Louisville), Xiang‐Dong Fu(University of California San Diego), Liang‐Hu Qu(Sun Yat-sen University), En-Duo Wang(Center for Excellence in Molecular Cell Science), Mo‐Fang Liu(Chinese Academy of Sciences)
Cell Research
May 2, 2014
Cited by 449Open Access
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Abstract

Spermatogenesis in mammals is characterized by two waves of piRNA expression: one corresponds to classic piRNAs responsible for silencing retrotransponsons and the second wave is predominantly derived from nontransposon intergenic regions in pachytene spermatocytes, but the function of these pachytene piRNAs is largely unknown. Here, we report the involvement of pachytene piRNAs in instructing massive mRNA elimination in mouse elongating spermatids (ES). We demonstrate that a piRNA-induced silencing complex (pi-RISC) containing murine PIWI (MIWI) and deadenylase CAF1 is selectively assembled in ES, which is responsible for inducing mRNA deadenylation and decay via a mechanism that resembles the action of miRNAs in somatic cells. Such a highly orchestrated program appears to take full advantage of the enormous repertoire of diversified targeting capacity of pachytene piRNAs derived from nontransposon intergenic regions. These findings suggest that pachytene piRNAs are responsible for inactivating vast cellular programs in preparation for sperm production from ES.


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