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The Structural Complexity of the Human BORIS Gene in Gametogenesis and Cancer

BACKGROUND: BORIS/CTCFL is a paralogue of CTCF, the major epigenetic regulator of vertebrate genomes. BORIS is normally expressed only in germ cells but is aberrantly activated in numerous cancers. While recent studies demonstrated that BORIS is a transcriptional activator of testis-specific genes,...

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Autores principales: Pugacheva, Elena M., Suzuki, Teruhiko, Pack, Svetlana D., Kosaka-Suzuki, Natsuki, Yoon, Jeongheon, Vostrov, Alexander A., Barsov, Eugene, Strunnikov, Alexander V., Morse, Herbert C., Loukinov, Dmitri, Lobanenkov, Victor
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2975627/
https://www.ncbi.nlm.nih.gov/pubmed/21079786
http://dx.doi.org/10.1371/journal.pone.0013872
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author Pugacheva, Elena M.
Suzuki, Teruhiko
Pack, Svetlana D.
Kosaka-Suzuki, Natsuki
Yoon, Jeongheon
Vostrov, Alexander A.
Barsov, Eugene
Strunnikov, Alexander V.
Morse, Herbert C.
Loukinov, Dmitri
Lobanenkov, Victor
author_facet Pugacheva, Elena M.
Suzuki, Teruhiko
Pack, Svetlana D.
Kosaka-Suzuki, Natsuki
Yoon, Jeongheon
Vostrov, Alexander A.
Barsov, Eugene
Strunnikov, Alexander V.
Morse, Herbert C.
Loukinov, Dmitri
Lobanenkov, Victor
author_sort Pugacheva, Elena M.
collection PubMed
description BACKGROUND: BORIS/CTCFL is a paralogue of CTCF, the major epigenetic regulator of vertebrate genomes. BORIS is normally expressed only in germ cells but is aberrantly activated in numerous cancers. While recent studies demonstrated that BORIS is a transcriptional activator of testis-specific genes, little is generally known about its biological and molecular functions. METHODOLOGY/PRINCIPAL FINDINGS: Here we show that BORIS is expressed as 23 isoforms in germline and cancer cells. The isoforms are comprised of alternative N- and C-termini combined with varying numbers of zinc fingers (ZF) in the DNA binding domain. The patterns of BORIS isoform expression are distinct in germ and cancer cells. Isoform expression is activated by downregulation of CTCF, upregulated by reduction in CpG methylation caused by inactivation of DNMT1 or DNMT3b, and repressed by activation of p53. Studies of ectopically expressed isoforms showed that all are translated and localized to the nucleus. Using the testis-specific cerebroside sulfotransferase (CST) promoter and the IGF2/H19 imprinting control region (ICR), it was shown that binding of BORIS isoforms to DNA targets in vitro is methylation-sensitive and depends on the number and specific composition of ZF. The ability to bind target DNA and the presence of a specific long amino terminus (N258) in different isoforms are necessary and sufficient to activate CST transcription. Comparative sequence analyses revealed an evolutionary burst in mammals with strong conservation of BORIS isoproteins among primates. CONCLUSIONS: The extensive repertoire of spliced BORIS variants in humans that confer distinct DNA binding and transcriptional activation properties, and their differential patterns of expression among germ cells and neoplastic cells suggest that the gene is involved in a range of functionally important aspects of both normal gametogenesis and cancer development. In addition, a burst in isoform diversification may be evolutionarily tied to unique aspects of primate speciation.
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spelling pubmed-29756272010-11-15 The Structural Complexity of the Human BORIS Gene in Gametogenesis and Cancer Pugacheva, Elena M. Suzuki, Teruhiko Pack, Svetlana D. Kosaka-Suzuki, Natsuki Yoon, Jeongheon Vostrov, Alexander A. Barsov, Eugene Strunnikov, Alexander V. Morse, Herbert C. Loukinov, Dmitri Lobanenkov, Victor PLoS One Research Article BACKGROUND: BORIS/CTCFL is a paralogue of CTCF, the major epigenetic regulator of vertebrate genomes. BORIS is normally expressed only in germ cells but is aberrantly activated in numerous cancers. While recent studies demonstrated that BORIS is a transcriptional activator of testis-specific genes, little is generally known about its biological and molecular functions. METHODOLOGY/PRINCIPAL FINDINGS: Here we show that BORIS is expressed as 23 isoforms in germline and cancer cells. The isoforms are comprised of alternative N- and C-termini combined with varying numbers of zinc fingers (ZF) in the DNA binding domain. The patterns of BORIS isoform expression are distinct in germ and cancer cells. Isoform expression is activated by downregulation of CTCF, upregulated by reduction in CpG methylation caused by inactivation of DNMT1 or DNMT3b, and repressed by activation of p53. Studies of ectopically expressed isoforms showed that all are translated and localized to the nucleus. Using the testis-specific cerebroside sulfotransferase (CST) promoter and the IGF2/H19 imprinting control region (ICR), it was shown that binding of BORIS isoforms to DNA targets in vitro is methylation-sensitive and depends on the number and specific composition of ZF. The ability to bind target DNA and the presence of a specific long amino terminus (N258) in different isoforms are necessary and sufficient to activate CST transcription. Comparative sequence analyses revealed an evolutionary burst in mammals with strong conservation of BORIS isoproteins among primates. CONCLUSIONS: The extensive repertoire of spliced BORIS variants in humans that confer distinct DNA binding and transcriptional activation properties, and their differential patterns of expression among germ cells and neoplastic cells suggest that the gene is involved in a range of functionally important aspects of both normal gametogenesis and cancer development. In addition, a burst in isoform diversification may be evolutionarily tied to unique aspects of primate speciation. Public Library of Science 2010-11-08 /pmc/articles/PMC2975627/ /pubmed/21079786 http://dx.doi.org/10.1371/journal.pone.0013872 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Pugacheva, Elena M.
Suzuki, Teruhiko
Pack, Svetlana D.
Kosaka-Suzuki, Natsuki
Yoon, Jeongheon
Vostrov, Alexander A.
Barsov, Eugene
Strunnikov, Alexander V.
Morse, Herbert C.
Loukinov, Dmitri
Lobanenkov, Victor
The Structural Complexity of the Human BORIS Gene in Gametogenesis and Cancer
title The Structural Complexity of the Human BORIS Gene in Gametogenesis and Cancer
title_full The Structural Complexity of the Human BORIS Gene in Gametogenesis and Cancer
title_fullStr The Structural Complexity of the Human BORIS Gene in Gametogenesis and Cancer
title_full_unstemmed The Structural Complexity of the Human BORIS Gene in Gametogenesis and Cancer
title_short The Structural Complexity of the Human BORIS Gene in Gametogenesis and Cancer
title_sort structural complexity of the human boris gene in gametogenesis and cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2975627/
https://www.ncbi.nlm.nih.gov/pubmed/21079786
http://dx.doi.org/10.1371/journal.pone.0013872
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