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MIR sequences recruit zinc finger protein ZNF768 to expressed genes

Mammalian-wide interspersed repeats (MIRs) are retrotransposed elements of mammalian genomes. Here, we report the specific binding of zinc finger protein ZNF768 to the sequence motif GCTGTGTG (N(20)) CCTCTCTG in the core region of MIRs. ZNF768 binding is preferentially associated with euchromatin an...

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Autores principales: Rohrmoser, Michaela, Kluge, Michael, Yahia, Yousra, Gruber-Eber, Anita, Maqbool, Muhammad Ahmad, Forné, Ignasi, Krebs, Stefan, Blum, Helmut, Greifenberg, Ann Katrin, Geyer, Matthias, Descostes, Nicolas, Imhof, Axel, Andrau, Jean-Christophe, Friedel, Caroline C, Eick, Dirk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344866/
https://www.ncbi.nlm.nih.gov/pubmed/30476274
http://dx.doi.org/10.1093/nar/gky1148
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author Rohrmoser, Michaela
Kluge, Michael
Yahia, Yousra
Gruber-Eber, Anita
Maqbool, Muhammad Ahmad
Forné, Ignasi
Krebs, Stefan
Blum, Helmut
Greifenberg, Ann Katrin
Geyer, Matthias
Descostes, Nicolas
Imhof, Axel
Andrau, Jean-Christophe
Friedel, Caroline C
Eick, Dirk
author_facet Rohrmoser, Michaela
Kluge, Michael
Yahia, Yousra
Gruber-Eber, Anita
Maqbool, Muhammad Ahmad
Forné, Ignasi
Krebs, Stefan
Blum, Helmut
Greifenberg, Ann Katrin
Geyer, Matthias
Descostes, Nicolas
Imhof, Axel
Andrau, Jean-Christophe
Friedel, Caroline C
Eick, Dirk
author_sort Rohrmoser, Michaela
collection PubMed
description Mammalian-wide interspersed repeats (MIRs) are retrotransposed elements of mammalian genomes. Here, we report the specific binding of zinc finger protein ZNF768 to the sequence motif GCTGTGTG (N(20)) CCTCTCTG in the core region of MIRs. ZNF768 binding is preferentially associated with euchromatin and promoter regions of genes. Binding was observed for genes expressed in a cell type-specific manner in human B cell line Raji and osteosarcoma U2OS cells. Mass spectrometric analysis revealed binding of ZNF768 to Elongator components Elp1, Elp2 and Elp3 and other nuclear factors. The N-terminus of ZNF768 contains a heptad repeat array structurally related to the C-terminal domain (CTD) of RNA polymerase II. This array evolved in placental animals but not marsupials and monotreme species, displays species-specific length variations, and possibly fulfills CTD related functions in gene regulation. We propose that the evolution of MIRs and ZNF768 has extended the repertoire of gene regulatory mechanisms in mammals and that ZNF768 binding is associated with cell type-specific gene expression.
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spelling pubmed-63448662019-01-29 MIR sequences recruit zinc finger protein ZNF768 to expressed genes Rohrmoser, Michaela Kluge, Michael Yahia, Yousra Gruber-Eber, Anita Maqbool, Muhammad Ahmad Forné, Ignasi Krebs, Stefan Blum, Helmut Greifenberg, Ann Katrin Geyer, Matthias Descostes, Nicolas Imhof, Axel Andrau, Jean-Christophe Friedel, Caroline C Eick, Dirk Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Mammalian-wide interspersed repeats (MIRs) are retrotransposed elements of mammalian genomes. Here, we report the specific binding of zinc finger protein ZNF768 to the sequence motif GCTGTGTG (N(20)) CCTCTCTG in the core region of MIRs. ZNF768 binding is preferentially associated with euchromatin and promoter regions of genes. Binding was observed for genes expressed in a cell type-specific manner in human B cell line Raji and osteosarcoma U2OS cells. Mass spectrometric analysis revealed binding of ZNF768 to Elongator components Elp1, Elp2 and Elp3 and other nuclear factors. The N-terminus of ZNF768 contains a heptad repeat array structurally related to the C-terminal domain (CTD) of RNA polymerase II. This array evolved in placental animals but not marsupials and monotreme species, displays species-specific length variations, and possibly fulfills CTD related functions in gene regulation. We propose that the evolution of MIRs and ZNF768 has extended the repertoire of gene regulatory mechanisms in mammals and that ZNF768 binding is associated with cell type-specific gene expression. Oxford University Press 2019-01-25 2018-11-22 /pmc/articles/PMC6344866/ /pubmed/30476274 http://dx.doi.org/10.1093/nar/gky1148 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Gene regulation, Chromatin and Epigenetics
Rohrmoser, Michaela
Kluge, Michael
Yahia, Yousra
Gruber-Eber, Anita
Maqbool, Muhammad Ahmad
Forné, Ignasi
Krebs, Stefan
Blum, Helmut
Greifenberg, Ann Katrin
Geyer, Matthias
Descostes, Nicolas
Imhof, Axel
Andrau, Jean-Christophe
Friedel, Caroline C
Eick, Dirk
MIR sequences recruit zinc finger protein ZNF768 to expressed genes
title MIR sequences recruit zinc finger protein ZNF768 to expressed genes
title_full MIR sequences recruit zinc finger protein ZNF768 to expressed genes
title_fullStr MIR sequences recruit zinc finger protein ZNF768 to expressed genes
title_full_unstemmed MIR sequences recruit zinc finger protein ZNF768 to expressed genes
title_short MIR sequences recruit zinc finger protein ZNF768 to expressed genes
title_sort mir sequences recruit zinc finger protein znf768 to expressed genes
topic Gene regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344866/
https://www.ncbi.nlm.nih.gov/pubmed/30476274
http://dx.doi.org/10.1093/nar/gky1148
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