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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2012-01-01
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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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