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The mouse genome displays highly dynamic populations of KRAB-zinc finger protein genes and related genetic units
KRAB-containing poly-zinc finger proteins (KZFPs) constitute the largest family of transcription factors encoded by mammalian genomes, and growing evidence indicates that they fulfill functions critical to both embryonic development and maintenance of adult homeostasis. KZFP genes underwent broad an...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363842/ https://www.ncbi.nlm.nih.gov/pubmed/28334004 http://dx.doi.org/10.1371/journal.pone.0173746 |
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author | Kauzlaric, Annamaria Ecco, Gabriela Cassano, Marco Duc, Julien Imbeault, Michael Trono, Didier |
author_facet | Kauzlaric, Annamaria Ecco, Gabriela Cassano, Marco Duc, Julien Imbeault, Michael Trono, Didier |
author_sort | Kauzlaric, Annamaria |
collection | PubMed |
description | KRAB-containing poly-zinc finger proteins (KZFPs) constitute the largest family of transcription factors encoded by mammalian genomes, and growing evidence indicates that they fulfill functions critical to both embryonic development and maintenance of adult homeostasis. KZFP genes underwent broad and independent waves of expansion in many higher vertebrates lineages, yet comprehensive studies of members harbored by a given species are scarce. Here we present a thorough analysis of KZFP genes and related units in the murine genome. We first identified about twice as many elements than previously annotated as either KZFP genes or pseudogenes, notably by assigning to this family an entity formerly considered as a large group of Satellite repeats. We then could delineate an organization in clusters distributed throughout the genome, with signs of recombination, translocation, duplication and seeding of new sites by retrotransposition of KZFP genes and related genetic units (KZFP/rGUs). Moreover, we harvested evidence indicating that closely related paralogs had evolved through both drifting and shifting of sequences encoding for zinc finger arrays. Finally, we could demonstrate that the KAP1-SETDB1 repressor complex tames the expression of KZFP/rGUs within clusters, yet that the primary targets of this regulation are not the KZFP/rGUs themselves but enhancers contained in neighboring endogenous retroelements and that, underneath, KZFPs conserve highly individualized patterns of expression. |
format | Online Article Text |
id | pubmed-5363842 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-53638422017-04-06 The mouse genome displays highly dynamic populations of KRAB-zinc finger protein genes and related genetic units Kauzlaric, Annamaria Ecco, Gabriela Cassano, Marco Duc, Julien Imbeault, Michael Trono, Didier PLoS One Research Article KRAB-containing poly-zinc finger proteins (KZFPs) constitute the largest family of transcription factors encoded by mammalian genomes, and growing evidence indicates that they fulfill functions critical to both embryonic development and maintenance of adult homeostasis. KZFP genes underwent broad and independent waves of expansion in many higher vertebrates lineages, yet comprehensive studies of members harbored by a given species are scarce. Here we present a thorough analysis of KZFP genes and related units in the murine genome. We first identified about twice as many elements than previously annotated as either KZFP genes or pseudogenes, notably by assigning to this family an entity formerly considered as a large group of Satellite repeats. We then could delineate an organization in clusters distributed throughout the genome, with signs of recombination, translocation, duplication and seeding of new sites by retrotransposition of KZFP genes and related genetic units (KZFP/rGUs). Moreover, we harvested evidence indicating that closely related paralogs had evolved through both drifting and shifting of sequences encoding for zinc finger arrays. Finally, we could demonstrate that the KAP1-SETDB1 repressor complex tames the expression of KZFP/rGUs within clusters, yet that the primary targets of this regulation are not the KZFP/rGUs themselves but enhancers contained in neighboring endogenous retroelements and that, underneath, KZFPs conserve highly individualized patterns of expression. Public Library of Science 2017-03-23 /pmc/articles/PMC5363842/ /pubmed/28334004 http://dx.doi.org/10.1371/journal.pone.0173746 Text en © 2017 Kauzlaric et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Kauzlaric, Annamaria Ecco, Gabriela Cassano, Marco Duc, Julien Imbeault, Michael Trono, Didier The mouse genome displays highly dynamic populations of KRAB-zinc finger protein genes and related genetic units |
title | The mouse genome displays highly dynamic populations of KRAB-zinc finger protein genes and related genetic units |
title_full | The mouse genome displays highly dynamic populations of KRAB-zinc finger protein genes and related genetic units |
title_fullStr | The mouse genome displays highly dynamic populations of KRAB-zinc finger protein genes and related genetic units |
title_full_unstemmed | The mouse genome displays highly dynamic populations of KRAB-zinc finger protein genes and related genetic units |
title_short | The mouse genome displays highly dynamic populations of KRAB-zinc finger protein genes and related genetic units |
title_sort | mouse genome displays highly dynamic populations of krab-zinc finger protein genes and related genetic units |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363842/ https://www.ncbi.nlm.nih.gov/pubmed/28334004 http://dx.doi.org/10.1371/journal.pone.0173746 |
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