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Genetic Interactions Between the Meiosis-Specific Cohesin Components, STAG3, REC8, and RAD21L

Cohesin is an essential structural component of chromosomes that ensures accurate chromosome segregation during mitosis and meiosis. Previous studies have shown that there are cohesin complexes specific to meiosis, required to mediate homologous chromosome pairing, synapsis, recombination, and segre...

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Autores principales: Ward, Ayobami, Hopkins, Jessica, Mckay, Matthew, Murray, Steve, Jordan, Philip W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4889667/
https://www.ncbi.nlm.nih.gov/pubmed/27172213
http://dx.doi.org/10.1534/g3.116.029462
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author Ward, Ayobami
Hopkins, Jessica
Mckay, Matthew
Murray, Steve
Jordan, Philip W.
author_facet Ward, Ayobami
Hopkins, Jessica
Mckay, Matthew
Murray, Steve
Jordan, Philip W.
author_sort Ward, Ayobami
collection PubMed
description Cohesin is an essential structural component of chromosomes that ensures accurate chromosome segregation during mitosis and meiosis. Previous studies have shown that there are cohesin complexes specific to meiosis, required to mediate homologous chromosome pairing, synapsis, recombination, and segregation. Meiosis-specific cohesin complexes consist of two structural maintenance of chromosomes proteins (SMC1α/SMC1β and SMC3), an α-kleisin protein (RAD21, RAD21L, or REC8), and a stromal antigen protein (STAG1, 2, or 3). STAG3 is exclusively expressed during meiosis, and is the predominant STAG protein component of cohesin complexes in primary spermatocytes from mouse, interacting directly with each α-kleisin subunit. REC8 and RAD21L are also meiosis-specific cohesin components. Stag3 mutant spermatocytes arrest in early prophase (“zygotene-like” stage), displaying failed homolog synapsis and persistent DNA damage, as a result of unstable loading of cohesin onto the chromosome axes. Interestingly, Rec8, Rad21L double mutants resulted in an earlier “leptotene-like” arrest, accompanied by complete absence of STAG3 loading. To assess genetic interactions between STAG3 and α-kleisin subunits RAD21L and REC8, our lab generated Stag3, Rad21L, and Stag3, Rec8 double knockout mice, and compared them to the Rec8, Rad21L double mutant. These double mutants are phenotypically distinct from one another, and more severe than each single knockout mutant with regards to chromosome axis formation, cohesin loading, and sister chromatid cohesion. The Stag3, Rad21L, and Stag3, Rec8 double mutants both progress further into prophase I than the Rec8, Rad21L double mutant. Our genetic analysis demonstrates that cohesins containing STAG3 and REC8 are the main complex required for centromeric cohesion, and RAD21L cohesins are required for normal clustering of pericentromeric heterochromatin. Furthermore, the STAG3/REC8 and STAG3/RAD21L cohesins are the primary cohesins required for axis formation.
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spelling pubmed-48896672016-06-02 Genetic Interactions Between the Meiosis-Specific Cohesin Components, STAG3, REC8, and RAD21L Ward, Ayobami Hopkins, Jessica Mckay, Matthew Murray, Steve Jordan, Philip W. G3 (Bethesda) Investigations Cohesin is an essential structural component of chromosomes that ensures accurate chromosome segregation during mitosis and meiosis. Previous studies have shown that there are cohesin complexes specific to meiosis, required to mediate homologous chromosome pairing, synapsis, recombination, and segregation. Meiosis-specific cohesin complexes consist of two structural maintenance of chromosomes proteins (SMC1α/SMC1β and SMC3), an α-kleisin protein (RAD21, RAD21L, or REC8), and a stromal antigen protein (STAG1, 2, or 3). STAG3 is exclusively expressed during meiosis, and is the predominant STAG protein component of cohesin complexes in primary spermatocytes from mouse, interacting directly with each α-kleisin subunit. REC8 and RAD21L are also meiosis-specific cohesin components. Stag3 mutant spermatocytes arrest in early prophase (“zygotene-like” stage), displaying failed homolog synapsis and persistent DNA damage, as a result of unstable loading of cohesin onto the chromosome axes. Interestingly, Rec8, Rad21L double mutants resulted in an earlier “leptotene-like” arrest, accompanied by complete absence of STAG3 loading. To assess genetic interactions between STAG3 and α-kleisin subunits RAD21L and REC8, our lab generated Stag3, Rad21L, and Stag3, Rec8 double knockout mice, and compared them to the Rec8, Rad21L double mutant. These double mutants are phenotypically distinct from one another, and more severe than each single knockout mutant with regards to chromosome axis formation, cohesin loading, and sister chromatid cohesion. The Stag3, Rad21L, and Stag3, Rec8 double mutants both progress further into prophase I than the Rec8, Rad21L double mutant. Our genetic analysis demonstrates that cohesins containing STAG3 and REC8 are the main complex required for centromeric cohesion, and RAD21L cohesins are required for normal clustering of pericentromeric heterochromatin. Furthermore, the STAG3/REC8 and STAG3/RAD21L cohesins are the primary cohesins required for axis formation. Genetics Society of America 2016-04-16 /pmc/articles/PMC4889667/ /pubmed/27172213 http://dx.doi.org/10.1534/g3.116.029462 Text en Copyright © 2016 Ward et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Ward, Ayobami
Hopkins, Jessica
Mckay, Matthew
Murray, Steve
Jordan, Philip W.
Genetic Interactions Between the Meiosis-Specific Cohesin Components, STAG3, REC8, and RAD21L
title Genetic Interactions Between the Meiosis-Specific Cohesin Components, STAG3, REC8, and RAD21L
title_full Genetic Interactions Between the Meiosis-Specific Cohesin Components, STAG3, REC8, and RAD21L
title_fullStr Genetic Interactions Between the Meiosis-Specific Cohesin Components, STAG3, REC8, and RAD21L
title_full_unstemmed Genetic Interactions Between the Meiosis-Specific Cohesin Components, STAG3, REC8, and RAD21L
title_short Genetic Interactions Between the Meiosis-Specific Cohesin Components, STAG3, REC8, and RAD21L
title_sort genetic interactions between the meiosis-specific cohesin components, stag3, rec8, and rad21l
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4889667/
https://www.ncbi.nlm.nih.gov/pubmed/27172213
http://dx.doi.org/10.1534/g3.116.029462
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