Cargando…

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)...

Descripción completa

Detalles Bibliográficos
Autores principales: Ding, Deqiang, Liu, Jiali, Dong, Kunzhe, Midic, Uros, Hess, Rex A., Xie, Huirong, Demireva, Elena Y., Chen, Chen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
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
_version_ 1783270193960583168
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
work_keys_str_mv AT dingdeqiang pnldc1isessentialforpirna3endtrimmingandtransposonsilencingduringspermatogenesisinmice
AT liujiali pnldc1isessentialforpirna3endtrimmingandtransposonsilencingduringspermatogenesisinmice
AT dongkunzhe pnldc1isessentialforpirna3endtrimmingandtransposonsilencingduringspermatogenesisinmice
AT midicuros pnldc1isessentialforpirna3endtrimmingandtransposonsilencingduringspermatogenesisinmice
AT hessrexa pnldc1isessentialforpirna3endtrimmingandtransposonsilencingduringspermatogenesisinmice
AT xiehuirong pnldc1isessentialforpirna3endtrimmingandtransposonsilencingduringspermatogenesisinmice
AT demirevaelenay pnldc1isessentialforpirna3endtrimmingandtransposonsilencingduringspermatogenesisinmice
AT chenchen pnldc1isessentialforpirna3endtrimmingandtransposonsilencingduringspermatogenesisinmice