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Alternative cleavage and polyadenylation in spermatogenesis connects chromatin regulation with post-transcriptional control

BACKGROUND: Most mammalian genes display alternative cleavage and polyadenylation (APA). Previous studies have indicated preferential expression of APA isoforms with short 3’ untranslated regions (3’UTRs) in testes. RESULTS: By deep sequencing of the 3’ end region of poly(A) + transcripts, we report...

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Autores principales: Li, Wencheng, Park, Ji Yeon, Zheng, Dinghai, Hoque, Mainul, Yehia, Ghassan, Tian, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4724118/
https://www.ncbi.nlm.nih.gov/pubmed/26801249
http://dx.doi.org/10.1186/s12915-016-0229-6
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author Li, Wencheng
Park, Ji Yeon
Zheng, Dinghai
Hoque, Mainul
Yehia, Ghassan
Tian, Bin
author_facet Li, Wencheng
Park, Ji Yeon
Zheng, Dinghai
Hoque, Mainul
Yehia, Ghassan
Tian, Bin
author_sort Li, Wencheng
collection PubMed
description BACKGROUND: Most mammalian genes display alternative cleavage and polyadenylation (APA). Previous studies have indicated preferential expression of APA isoforms with short 3’ untranslated regions (3’UTRs) in testes. RESULTS: By deep sequencing of the 3’ end region of poly(A) + transcripts, we report widespread shortening of 3’UTR through APA during the first wave of spermatogenesis in mouse, with 3’UTR size being the shortest in spermatids. Using genes without APA as a control, we show that shortening of 3’UTR eliminates destabilizing elements, such as U-rich elements and transposable elements, which appear highly potent during spermatogenesis. We additionally found widespread regulation of APA events in introns and exons that can affect the coding sequence of transcripts and global activation of antisense transcripts upstream of the transcription start site, suggesting modulation of splicing and initiation of transcription during spermatogenesis. Importantly, genes that display significant 3’UTR shortening tend to have functions critical for further sperm maturation, and testis-specific genes display greater 3’UTR shortening than ubiquitously expressed ones, indicating functional relevance of APA to spermatogenesis. Interestingly, genes with shortened 3’UTRs tend to have higher RNA polymerase II and H3K4me3 levels in spermatids as compared to spermatocytes, features previously known to be associated with open chromatin state. CONCLUSIONS: Our data suggest that open chromatin may create a favorable cis environment for 3’ end processing, leading to global shortening of 3’UTR during spermatogenesis. mRNAs with shortened 3’UTRs are relatively stable thanks to evasion of powerful mRNA degradation mechanisms acting on 3’UTR elements. Stable mRNAs generated in spermatids may be important for protein production at later stages of sperm maturation, when transcription is globally halted. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-016-0229-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-47241182016-01-24 Alternative cleavage and polyadenylation in spermatogenesis connects chromatin regulation with post-transcriptional control Li, Wencheng Park, Ji Yeon Zheng, Dinghai Hoque, Mainul Yehia, Ghassan Tian, Bin BMC Biol Research Article BACKGROUND: Most mammalian genes display alternative cleavage and polyadenylation (APA). Previous studies have indicated preferential expression of APA isoforms with short 3’ untranslated regions (3’UTRs) in testes. RESULTS: By deep sequencing of the 3’ end region of poly(A) + transcripts, we report widespread shortening of 3’UTR through APA during the first wave of spermatogenesis in mouse, with 3’UTR size being the shortest in spermatids. Using genes without APA as a control, we show that shortening of 3’UTR eliminates destabilizing elements, such as U-rich elements and transposable elements, which appear highly potent during spermatogenesis. We additionally found widespread regulation of APA events in introns and exons that can affect the coding sequence of transcripts and global activation of antisense transcripts upstream of the transcription start site, suggesting modulation of splicing and initiation of transcription during spermatogenesis. Importantly, genes that display significant 3’UTR shortening tend to have functions critical for further sperm maturation, and testis-specific genes display greater 3’UTR shortening than ubiquitously expressed ones, indicating functional relevance of APA to spermatogenesis. Interestingly, genes with shortened 3’UTRs tend to have higher RNA polymerase II and H3K4me3 levels in spermatids as compared to spermatocytes, features previously known to be associated with open chromatin state. CONCLUSIONS: Our data suggest that open chromatin may create a favorable cis environment for 3’ end processing, leading to global shortening of 3’UTR during spermatogenesis. mRNAs with shortened 3’UTRs are relatively stable thanks to evasion of powerful mRNA degradation mechanisms acting on 3’UTR elements. Stable mRNAs generated in spermatids may be important for protein production at later stages of sperm maturation, when transcription is globally halted. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-016-0229-6) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-22 /pmc/articles/PMC4724118/ /pubmed/26801249 http://dx.doi.org/10.1186/s12915-016-0229-6 Text en © Li et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Li, Wencheng
Park, Ji Yeon
Zheng, Dinghai
Hoque, Mainul
Yehia, Ghassan
Tian, Bin
Alternative cleavage and polyadenylation in spermatogenesis connects chromatin regulation with post-transcriptional control
title Alternative cleavage and polyadenylation in spermatogenesis connects chromatin regulation with post-transcriptional control
title_full Alternative cleavage and polyadenylation in spermatogenesis connects chromatin regulation with post-transcriptional control
title_fullStr Alternative cleavage and polyadenylation in spermatogenesis connects chromatin regulation with post-transcriptional control
title_full_unstemmed Alternative cleavage and polyadenylation in spermatogenesis connects chromatin regulation with post-transcriptional control
title_short Alternative cleavage and polyadenylation in spermatogenesis connects chromatin regulation with post-transcriptional control
title_sort alternative cleavage and polyadenylation in spermatogenesis connects chromatin regulation with post-transcriptional control
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4724118/
https://www.ncbi.nlm.nih.gov/pubmed/26801249
http://dx.doi.org/10.1186/s12915-016-0229-6
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