PNLDC1, mouse pre‐piRNA Trimmer,is required for meiotic and post‐meiotic male germ cell development |
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Authors: | Tsunetoshi Nakatani Natsuko Izumi Yukihide Tomari Satomi Kuramochi‐Miyagawa Toru Nakano |
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Affiliation: | 1. Department of Pathology, Osaka University, Suita, Osaka, Japan;2. Institute of Molecular and Cellular Biosciences, The University of Tokyo, Bunkyo‐ku, Tokyo, Japan;3. Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Bunkyo‐ku, Tokyo, Japan;4. CREST, Japan Science and Technology Agency (JST), Saitama, Japan;5. Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka, Japan |
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Abstract: | PIWI‐interacting RNAs (piRNAs) are germ cell‐specific small RNAs essential for retrotransposon gene silencing and male germ cell development. In piRNA biogenesis, the endonuclease MitoPLD/Zucchini cleaves long, single‐stranded RNAs to generate 5′ termini of precursor piRNAs (pre‐piRNAs) that are consecutively loaded into PIWI‐family proteins. Subsequently, these pre‐piRNAs are trimmed at their 3′‐end by an exonuclease called Trimmer. Recently, poly(A)‐specific ribonuclease‐like domain‐containing 1 (PNLDC1) was identified as the pre‐piRNA Trimmer in silkworms. However, the function of PNLDC1 in other species remains unknown. Here, we generate Pnldc1 mutant mice and analyze small RNAs in their testes. Our results demonstrate that mouse PNLDC1 functions in the trimming of both embryonic and post‐natal pre‐piRNAs. In addition, piRNA trimming defects in embryonic and post‐natal testes cause impaired DNA methylation and reduced MIWI expression, respectively. Phenotypically, both meiotic and post‐meiotic arrests are evident in the same individual Pnldc1 mutant mouse. The former and latter phenotypes are similar to those of MILI and MIWI mutant mice, respectively. Thus, PNLDC1‐mediated piRNA trimming is indispensable for the function of piRNAs throughout mouse spermatogenesis. |
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Keywords: | piRNA
PIWI
PNLDC1 spermatogenesis Trimmer |
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