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Recurrent Losses and Rapid Evolution of the Condensin II Complex in Insects

Condensins play a crucial role in the organization of genetic material by compacting and disentangling chromosomes. Based on studies in a few model organisms, the condensins I and II complexes are considered to have distinct functions, with the condensin II complex playing a role in meiosis and soma...

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Autores principales: King, Thomas D, Leonard, Christopher J, Cooper, Jacob C, Nguyen, Son, Joyce, Eric F, Phadnis, Nitin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759200/
https://www.ncbi.nlm.nih.gov/pubmed/31270536
http://dx.doi.org/10.1093/molbev/msz140
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author King, Thomas D
Leonard, Christopher J
Cooper, Jacob C
Nguyen, Son
Joyce, Eric F
Phadnis, Nitin
author_facet King, Thomas D
Leonard, Christopher J
Cooper, Jacob C
Nguyen, Son
Joyce, Eric F
Phadnis, Nitin
author_sort King, Thomas D
collection PubMed
description Condensins play a crucial role in the organization of genetic material by compacting and disentangling chromosomes. Based on studies in a few model organisms, the condensins I and II complexes are considered to have distinct functions, with the condensin II complex playing a role in meiosis and somatic pairing of homologous chromosomes in Drosophila. Intriguingly, the Cap-G2 subunit of condensin II is absent in Drosophila melanogaster, and this loss may be related to the high levels of chromosome pairing seen in flies. Here, we find that all three non-SMC subunits of condensin II (Cap-G2, Cap-D3, and Cap-H2) have been repeatedly and independently lost in taxa representing multiple insect orders, with some taxa lacking all three. We also find that all non-Dipteran insects display near-uniform low-pairing levels regardless of their condensin II complex composition, suggesting that some key aspects of genome organization are robust to condensin II subunit losses. Finally, we observe consistent signatures of positive selection in condensin subunits across flies and mammals. These findings suggest that these ancient complexes are far more evolutionarily labile than previously suspected, and are at the crossroads of several forms of genomic conflicts. Our results raise fundamental questions about the specific functions of the two condensin complexes in taxa that have experienced subunit losses, and open the door to further investigations to elucidate the diversity of molecular mechanisms that underlie genome organization across various life forms.
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spelling pubmed-67592002019-10-02 Recurrent Losses and Rapid Evolution of the Condensin II Complex in Insects King, Thomas D Leonard, Christopher J Cooper, Jacob C Nguyen, Son Joyce, Eric F Phadnis, Nitin Mol Biol Evol Discoveries Condensins play a crucial role in the organization of genetic material by compacting and disentangling chromosomes. Based on studies in a few model organisms, the condensins I and II complexes are considered to have distinct functions, with the condensin II complex playing a role in meiosis and somatic pairing of homologous chromosomes in Drosophila. Intriguingly, the Cap-G2 subunit of condensin II is absent in Drosophila melanogaster, and this loss may be related to the high levels of chromosome pairing seen in flies. Here, we find that all three non-SMC subunits of condensin II (Cap-G2, Cap-D3, and Cap-H2) have been repeatedly and independently lost in taxa representing multiple insect orders, with some taxa lacking all three. We also find that all non-Dipteran insects display near-uniform low-pairing levels regardless of their condensin II complex composition, suggesting that some key aspects of genome organization are robust to condensin II subunit losses. Finally, we observe consistent signatures of positive selection in condensin subunits across flies and mammals. These findings suggest that these ancient complexes are far more evolutionarily labile than previously suspected, and are at the crossroads of several forms of genomic conflicts. Our results raise fundamental questions about the specific functions of the two condensin complexes in taxa that have experienced subunit losses, and open the door to further investigations to elucidate the diversity of molecular mechanisms that underlie genome organization across various life forms. Oxford University Press 2019-10 2019-07-04 /pmc/articles/PMC6759200/ /pubmed/31270536 http://dx.doi.org/10.1093/molbev/msz140 Text en The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Discoveries
King, Thomas D
Leonard, Christopher J
Cooper, Jacob C
Nguyen, Son
Joyce, Eric F
Phadnis, Nitin
Recurrent Losses and Rapid Evolution of the Condensin II Complex in Insects
title Recurrent Losses and Rapid Evolution of the Condensin II Complex in Insects
title_full Recurrent Losses and Rapid Evolution of the Condensin II Complex in Insects
title_fullStr Recurrent Losses and Rapid Evolution of the Condensin II Complex in Insects
title_full_unstemmed Recurrent Losses and Rapid Evolution of the Condensin II Complex in Insects
title_short Recurrent Losses and Rapid Evolution of the Condensin II Complex in Insects
title_sort recurrent losses and rapid evolution of the condensin ii complex in insects
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759200/
https://www.ncbi.nlm.nih.gov/pubmed/31270536
http://dx.doi.org/10.1093/molbev/msz140
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