{"title":"减数分裂重组的生物化学:重组中间体的形成、处理和分解","authors":"Kirk T Ehmsen, Wolf-Dietrich Heyer","doi":"10.1007/7050_2008_039","DOIUrl":null,"url":null,"abstract":"<p><p>Meiotic recombination ensures accurate chromosome segregation during the first meiotic division and provides a mechanism to increase genetic heterogeneity among the meiotic products. Unlike homologous recombination in somatic (vegetative) cells, where sister chromatid interactions prevail and crossover formation is avoided, meiotic recombination is targeted to involve homologs, resulting in crossovers to connect the homologs before anaphase of the first meiotic division. The mechanisms responsible for homolog choice and crossover control are poorly understood, but likely involve meiosis-specific recombination proteins, as well as meiosis-specific chromosome organization and architecture. Much progress has been made to identify and biochemically characterize many of the proteins acting during meiotic recombination. This review will focus on the proteins that generate and process heteroduplex DNA, as well as those that process DNA junctions during meiotic recombination, with particular attention to how recombination activities promote crossover resolution between homologs.</p>","PeriodicalId":88493,"journal":{"name":"Genome dynamics and stability","volume":"3 ","pages":"91"},"PeriodicalIF":0.0000,"publicationDate":"2008-04-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2809983/pdf/nihms155146.pdf","citationCount":"0","resultStr":"{\"title\":\"Biochemistry of Meiotic Recombination: Formation, Processing, and Resolution of Recombination Intermediates.\",\"authors\":\"Kirk T Ehmsen, Wolf-Dietrich Heyer\",\"doi\":\"10.1007/7050_2008_039\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Meiotic recombination ensures accurate chromosome segregation during the first meiotic division and provides a mechanism to increase genetic heterogeneity among the meiotic products. Unlike homologous recombination in somatic (vegetative) cells, where sister chromatid interactions prevail and crossover formation is avoided, meiotic recombination is targeted to involve homologs, resulting in crossovers to connect the homologs before anaphase of the first meiotic division. The mechanisms responsible for homolog choice and crossover control are poorly understood, but likely involve meiosis-specific recombination proteins, as well as meiosis-specific chromosome organization and architecture. Much progress has been made to identify and biochemically characterize many of the proteins acting during meiotic recombination. This review will focus on the proteins that generate and process heteroduplex DNA, as well as those that process DNA junctions during meiotic recombination, with particular attention to how recombination activities promote crossover resolution between homologs.</p>\",\"PeriodicalId\":88493,\"journal\":{\"name\":\"Genome dynamics and stability\",\"volume\":\"3 \",\"pages\":\"91\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2008-04-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2809983/pdf/nihms155146.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Genome dynamics and stability\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1007/7050_2008_039\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genome dynamics and stability","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/7050_2008_039","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
减数分裂重组确保了减数第一次分裂期间染色体的准确分离,并提供了一种增加减数分裂产物遗传异质性的机制。与体细胞(无性生殖细胞)中的同源重组不同,减数分裂中的同源重组主要是姐妹染色单体之间的相互作用,避免交叉形成,而减数分裂重组的目标是涉及同源染色体,从而导致交叉,在减数第一次分裂的无丝分裂之前将同源染色体连接起来。目前对同源物选择和交叉控制的机制了解不多,但可能涉及减数分裂特异性重组蛋白以及减数分裂特异性染色体组织和结构。在对减数分裂重组过程中起作用的许多蛋白质进行鉴定和生物化学特征描述方面取得了很大进展。本综述将重点介绍在减数分裂重组过程中产生和处理异源双链 DNA 的蛋白质,以及处理 DNA 连接的蛋白质,尤其关注重组活动如何促进同源物之间的交叉解析。
Biochemistry of Meiotic Recombination: Formation, Processing, and Resolution of Recombination Intermediates.
Meiotic recombination ensures accurate chromosome segregation during the first meiotic division and provides a mechanism to increase genetic heterogeneity among the meiotic products. Unlike homologous recombination in somatic (vegetative) cells, where sister chromatid interactions prevail and crossover formation is avoided, meiotic recombination is targeted to involve homologs, resulting in crossovers to connect the homologs before anaphase of the first meiotic division. The mechanisms responsible for homolog choice and crossover control are poorly understood, but likely involve meiosis-specific recombination proteins, as well as meiosis-specific chromosome organization and architecture. Much progress has been made to identify and biochemically characterize many of the proteins acting during meiotic recombination. This review will focus on the proteins that generate and process heteroduplex DNA, as well as those that process DNA junctions during meiotic recombination, with particular attention to how recombination activities promote crossover resolution between homologs.