The τCstF-64 polyadenylation protein controls genome expression in testis.

The τCstF-64 polyadenylation protein (gene symbol Cstf2t) is a testis-expressed orthologue of CstF-64. Mice in which Cstf2t was knocked out had a phenotype that was only detected in meiotic and postmeiotic male germ cells, giving us the opportunity to examine CstF-64 function in an isolated developm...

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Main Authors: Wencheng Li, Hsiang-Jui Yeh, Ganesh S Shankarling, Zhe Ji, Bin Tian, Clinton C MacDonald
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3482194?pdf=render
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spelling doaj-dc6f5735e9704200903996ddfdf2fdef2020-11-25T02:32:14ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01710e4837310.1371/journal.pone.0048373The τCstF-64 polyadenylation protein controls genome expression in testis.Wencheng LiHsiang-Jui YehGanesh S ShankarlingZhe JiBin TianClinton C MacDonaldThe τCstF-64 polyadenylation protein (gene symbol Cstf2t) is a testis-expressed orthologue of CstF-64. Mice in which Cstf2t was knocked out had a phenotype that was only detected in meiotic and postmeiotic male germ cells, giving us the opportunity to examine CstF-64 function in an isolated developmental system. We performed massively parallel clonally amplified sequencing of cDNAs from testes of wild type and Cstf2t(-/-) mice. These results revealed that loss of τCstF-64 resulted in large-scale changes in patterns of genome expression. We determined that there was a significant overrepresentation of RNAs from introns and intergenic regions in testes of Cstf2t(-/-) mice, and a concomitant use of more distal polyadenylation sites. We observed this effect particularly in intronless small genes, many of which are expressed retroposons that likely co-evolved with τCstF-64. Finally, we observed overexpression of long interspersed nuclear element (LINE) sequences in Cstf2t(-/-) testes. These results suggest that τCstF-64 plays a role in 3' end determination and transcription termination for a large range of germ cell-expressed genes.http://europepmc.org/articles/PMC3482194?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Wencheng Li
Hsiang-Jui Yeh
Ganesh S Shankarling
Zhe Ji
Bin Tian
Clinton C MacDonald
spellingShingle Wencheng Li
Hsiang-Jui Yeh
Ganesh S Shankarling
Zhe Ji
Bin Tian
Clinton C MacDonald
The τCstF-64 polyadenylation protein controls genome expression in testis.
PLoS ONE
author_facet Wencheng Li
Hsiang-Jui Yeh
Ganesh S Shankarling
Zhe Ji
Bin Tian
Clinton C MacDonald
author_sort Wencheng Li
title The τCstF-64 polyadenylation protein controls genome expression in testis.
title_short The τCstF-64 polyadenylation protein controls genome expression in testis.
title_full The τCstF-64 polyadenylation protein controls genome expression in testis.
title_fullStr The τCstF-64 polyadenylation protein controls genome expression in testis.
title_full_unstemmed The τCstF-64 polyadenylation protein controls genome expression in testis.
title_sort τcstf-64 polyadenylation protein controls genome expression in testis.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description The τCstF-64 polyadenylation protein (gene symbol Cstf2t) is a testis-expressed orthologue of CstF-64. Mice in which Cstf2t was knocked out had a phenotype that was only detected in meiotic and postmeiotic male germ cells, giving us the opportunity to examine CstF-64 function in an isolated developmental system. We performed massively parallel clonally amplified sequencing of cDNAs from testes of wild type and Cstf2t(-/-) mice. These results revealed that loss of τCstF-64 resulted in large-scale changes in patterns of genome expression. We determined that there was a significant overrepresentation of RNAs from introns and intergenic regions in testes of Cstf2t(-/-) mice, and a concomitant use of more distal polyadenylation sites. We observed this effect particularly in intronless small genes, many of which are expressed retroposons that likely co-evolved with τCstF-64. Finally, we observed overexpression of long interspersed nuclear element (LINE) sequences in Cstf2t(-/-) testes. These results suggest that τCstF-64 plays a role in 3' end determination and transcription termination for a large range of germ cell-expressed genes.
url http://europepmc.org/articles/PMC3482194?pdf=render
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