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Crossover patterns under meiotic chromosome program

Repairing DNA double-strand breaks (DSBs) with homologous chromosomes as templates is the hallmark of meiosis. The critical outcome of meiotic homologous recombination is crossovers, which ensure faithful chromosome segregation and promote genetic diversity of progenies. Crossover patterns are tight...

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Autores principales: Wang, Shunxin, Shang, Yongliang, Liu, Yanlei, Zhai, Binyuan, Yang, Xiao, Zhang, Liangran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577264/
https://www.ncbi.nlm.nih.gov/pubmed/33533735
http://dx.doi.org/10.4103/aja.aja_86_20
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author Wang, Shunxin
Shang, Yongliang
Liu, Yanlei
Zhai, Binyuan
Yang, Xiao
Zhang, Liangran
author_facet Wang, Shunxin
Shang, Yongliang
Liu, Yanlei
Zhai, Binyuan
Yang, Xiao
Zhang, Liangran
author_sort Wang, Shunxin
collection PubMed
description Repairing DNA double-strand breaks (DSBs) with homologous chromosomes as templates is the hallmark of meiosis. The critical outcome of meiotic homologous recombination is crossovers, which ensure faithful chromosome segregation and promote genetic diversity of progenies. Crossover patterns are tightly controlled and exhibit three characteristics: obligatory crossover, crossover interference, and crossover homeostasis. Aberrant crossover patterns are the leading cause of infertility, miscarriage, and congenital disease. Crossover recombination occurs in the context of meiotic chromosomes, and it is tightly integrated with and regulated by meiotic chromosome structure both locally and globally. Meiotic chromosomes are organized in a loop-axis architecture. Diverse evidence shows that chromosome axis length determines crossover frequency. Interestingly, short chromosomes show different crossover patterns compared to long chromosomes. A high frequency of human embryos are aneuploid, primarily derived from female meiosis errors. Dramatically increased aneuploidy in older women is the well-known “maternal age effect.” However, a high frequency of aneuploidy also occurs in young women, derived from crossover maturation inefficiency in human females. In addition, frequency of human aneuploidy also shows other age-dependent alterations. Here, current advances in the understanding of these issues are reviewed, regulation of crossover patterns by meiotic chromosomes are discussed, and issues that remain to be investigated are suggested.
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spelling pubmed-85772642021-11-10 Crossover patterns under meiotic chromosome program Wang, Shunxin Shang, Yongliang Liu, Yanlei Zhai, Binyuan Yang, Xiao Zhang, Liangran Asian J Androl Invited Review Repairing DNA double-strand breaks (DSBs) with homologous chromosomes as templates is the hallmark of meiosis. The critical outcome of meiotic homologous recombination is crossovers, which ensure faithful chromosome segregation and promote genetic diversity of progenies. Crossover patterns are tightly controlled and exhibit three characteristics: obligatory crossover, crossover interference, and crossover homeostasis. Aberrant crossover patterns are the leading cause of infertility, miscarriage, and congenital disease. Crossover recombination occurs in the context of meiotic chromosomes, and it is tightly integrated with and regulated by meiotic chromosome structure both locally and globally. Meiotic chromosomes are organized in a loop-axis architecture. Diverse evidence shows that chromosome axis length determines crossover frequency. Interestingly, short chromosomes show different crossover patterns compared to long chromosomes. A high frequency of human embryos are aneuploid, primarily derived from female meiosis errors. Dramatically increased aneuploidy in older women is the well-known “maternal age effect.” However, a high frequency of aneuploidy also occurs in young women, derived from crossover maturation inefficiency in human females. In addition, frequency of human aneuploidy also shows other age-dependent alterations. Here, current advances in the understanding of these issues are reviewed, regulation of crossover patterns by meiotic chromosomes are discussed, and issues that remain to be investigated are suggested. Wolters Kluwer - Medknow 2021-01-26 /pmc/articles/PMC8577264/ /pubmed/33533735 http://dx.doi.org/10.4103/aja.aja_86_20 Text en Copyright: © The Author(s)(2021) https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Invited Review
Wang, Shunxin
Shang, Yongliang
Liu, Yanlei
Zhai, Binyuan
Yang, Xiao
Zhang, Liangran
Crossover patterns under meiotic chromosome program
title Crossover patterns under meiotic chromosome program
title_full Crossover patterns under meiotic chromosome program
title_fullStr Crossover patterns under meiotic chromosome program
title_full_unstemmed Crossover patterns under meiotic chromosome program
title_short Crossover patterns under meiotic chromosome program
title_sort crossover patterns under meiotic chromosome program
topic Invited Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577264/
https://www.ncbi.nlm.nih.gov/pubmed/33533735
http://dx.doi.org/10.4103/aja.aja_86_20
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