Cargando…
Chromosome architecture and homologous recombination in meiosis
Meiocytes organize higher-order chromosome structures comprising arrays of chromatin loops organized at their bases by linear axes. As meiotic prophase progresses, the axes of homologous chromosomes align and synapse along their lengths to form ladder-like structures called synaptonemal complexes (S...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9853400/ https://www.ncbi.nlm.nih.gov/pubmed/36684419 http://dx.doi.org/10.3389/fcell.2022.1097446 |
_version_ | 1784872890610483200 |
---|---|
author | Ito, Masaru Shinohara, Akira |
author_facet | Ito, Masaru Shinohara, Akira |
author_sort | Ito, Masaru |
collection | PubMed |
description | Meiocytes organize higher-order chromosome structures comprising arrays of chromatin loops organized at their bases by linear axes. As meiotic prophase progresses, the axes of homologous chromosomes align and synapse along their lengths to form ladder-like structures called synaptonemal complexes (SCs). The entire process of meiotic recombination, from initiation via programmed DNA double-strand breaks (DSBs) to completion of DSB repair with crossover or non-crossover outcomes, occurs in the context of chromosome axes and SCs. These meiosis-specific chromosome structures provide specialized environments for the regulation of DSB formation and crossing over. In this review, we summarize insights into the importance of chromosome architecture in the regulation of meiotic recombination, focusing on cohesin-mediated axis formation, DSB regulation via tethered loop-axis complexes, inter-homolog template bias facilitated by axial proteins, and crossover regulation in the context of the SCs. We also discuss emerging evidence that the SUMO and the ubiquitin-proteasome system function in the organization of chromosome structure and regulation of meiotic recombination. |
format | Online Article Text |
id | pubmed-9853400 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98534002023-01-21 Chromosome architecture and homologous recombination in meiosis Ito, Masaru Shinohara, Akira Front Cell Dev Biol Cell and Developmental Biology Meiocytes organize higher-order chromosome structures comprising arrays of chromatin loops organized at their bases by linear axes. As meiotic prophase progresses, the axes of homologous chromosomes align and synapse along their lengths to form ladder-like structures called synaptonemal complexes (SCs). The entire process of meiotic recombination, from initiation via programmed DNA double-strand breaks (DSBs) to completion of DSB repair with crossover or non-crossover outcomes, occurs in the context of chromosome axes and SCs. These meiosis-specific chromosome structures provide specialized environments for the regulation of DSB formation and crossing over. In this review, we summarize insights into the importance of chromosome architecture in the regulation of meiotic recombination, focusing on cohesin-mediated axis formation, DSB regulation via tethered loop-axis complexes, inter-homolog template bias facilitated by axial proteins, and crossover regulation in the context of the SCs. We also discuss emerging evidence that the SUMO and the ubiquitin-proteasome system function in the organization of chromosome structure and regulation of meiotic recombination. Frontiers Media S.A. 2023-01-06 /pmc/articles/PMC9853400/ /pubmed/36684419 http://dx.doi.org/10.3389/fcell.2022.1097446 Text en Copyright © 2023 Ito and Shinohara. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Ito, Masaru Shinohara, Akira Chromosome architecture and homologous recombination in meiosis |
title | Chromosome architecture and homologous recombination in meiosis |
title_full | Chromosome architecture and homologous recombination in meiosis |
title_fullStr | Chromosome architecture and homologous recombination in meiosis |
title_full_unstemmed | Chromosome architecture and homologous recombination in meiosis |
title_short | Chromosome architecture and homologous recombination in meiosis |
title_sort | chromosome architecture and homologous recombination in meiosis |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9853400/ https://www.ncbi.nlm.nih.gov/pubmed/36684419 http://dx.doi.org/10.3389/fcell.2022.1097446 |
work_keys_str_mv | AT itomasaru chromosomearchitectureandhomologousrecombinationinmeiosis AT shinoharaakira chromosomearchitectureandhomologousrecombinationinmeiosis |