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PNLDC1 is essential for piRNA 3′ end trimming and transposon silencing during spermatogenesis in mice
Piwi-interacting RNAs are small regulatory RNAs with key roles in transposon silencing and regulation of gametogenesis. The production of mature piwi-interacting RNAs requires a critical step of trimming piwi-interacting RNA intermediates to achieve optimally sized piwi-interacting RNAs. The poly(A)...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5635004/ https://www.ncbi.nlm.nih.gov/pubmed/29018194 http://dx.doi.org/10.1038/s41467-017-00854-4 |
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author | Ding, Deqiang Liu, Jiali Dong, Kunzhe Midic, Uros Hess, Rex A. Xie, Huirong Demireva, Elena Y. Chen, Chen |
author_facet | Ding, Deqiang Liu, Jiali Dong, Kunzhe Midic, Uros Hess, Rex A. Xie, Huirong Demireva, Elena Y. Chen, Chen |
author_sort | Ding, Deqiang |
collection | PubMed |
description | Piwi-interacting RNAs are small regulatory RNAs with key roles in transposon silencing and regulation of gametogenesis. The production of mature piwi-interacting RNAs requires a critical step of trimming piwi-interacting RNA intermediates to achieve optimally sized piwi-interacting RNAs. The poly(A)-specific ribonuclease family deadenylase PNLDC1 is implicated in piwi-interacting RNA trimming in silkworms. The physiological function of PNLDC1 in mammals remains unknown. Using Pnldc1-deficient mice, here we show that PNLDC1 is required for piwi-interacting RNA biogenesis, transposon silencing, and spermatogenesis. Pnldc1 mutation in mice inhibits piwi-interacting RNA trimming and causes accumulation of untrimmed piwi-interacting RNA intermediates with 3′ end extension, leading to severe reduction of mature piwi-interacting RNAs in the testis. Pnldc1 mutant mice exhibit disrupted LINE1 retrotransposon silencing and defect in spermiogenesis. Together, these results define PNLDC1 as a mammalian piwi-interacting RNA biogenesis factor that protects the germline genome and ensures normal sperm production in mice. |
format | Online Article Text |
id | pubmed-5635004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56350042017-10-12 PNLDC1 is essential for piRNA 3′ end trimming and transposon silencing during spermatogenesis in mice Ding, Deqiang Liu, Jiali Dong, Kunzhe Midic, Uros Hess, Rex A. Xie, Huirong Demireva, Elena Y. Chen, Chen Nat Commun Article Piwi-interacting RNAs are small regulatory RNAs with key roles in transposon silencing and regulation of gametogenesis. The production of mature piwi-interacting RNAs requires a critical step of trimming piwi-interacting RNA intermediates to achieve optimally sized piwi-interacting RNAs. The poly(A)-specific ribonuclease family deadenylase PNLDC1 is implicated in piwi-interacting RNA trimming in silkworms. The physiological function of PNLDC1 in mammals remains unknown. Using Pnldc1-deficient mice, here we show that PNLDC1 is required for piwi-interacting RNA biogenesis, transposon silencing, and spermatogenesis. Pnldc1 mutation in mice inhibits piwi-interacting RNA trimming and causes accumulation of untrimmed piwi-interacting RNA intermediates with 3′ end extension, leading to severe reduction of mature piwi-interacting RNAs in the testis. Pnldc1 mutant mice exhibit disrupted LINE1 retrotransposon silencing and defect in spermiogenesis. Together, these results define PNLDC1 as a mammalian piwi-interacting RNA biogenesis factor that protects the germline genome and ensures normal sperm production in mice. Nature Publishing Group UK 2017-10-10 /pmc/articles/PMC5635004/ /pubmed/29018194 http://dx.doi.org/10.1038/s41467-017-00854-4 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ding, Deqiang Liu, Jiali Dong, Kunzhe Midic, Uros Hess, Rex A. Xie, Huirong Demireva, Elena Y. Chen, Chen PNLDC1 is essential for piRNA 3′ end trimming and transposon silencing during spermatogenesis in mice |
title | PNLDC1 is essential for piRNA 3′ end trimming and transposon silencing during spermatogenesis in mice |
title_full | PNLDC1 is essential for piRNA 3′ end trimming and transposon silencing during spermatogenesis in mice |
title_fullStr | PNLDC1 is essential for piRNA 3′ end trimming and transposon silencing during spermatogenesis in mice |
title_full_unstemmed | PNLDC1 is essential for piRNA 3′ end trimming and transposon silencing during spermatogenesis in mice |
title_short | PNLDC1 is essential for piRNA 3′ end trimming and transposon silencing during spermatogenesis in mice |
title_sort | pnldc1 is essential for pirna 3′ end trimming and transposon silencing during spermatogenesis in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5635004/ https://www.ncbi.nlm.nih.gov/pubmed/29018194 http://dx.doi.org/10.1038/s41467-017-00854-4 |
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