Osman Kim, Algopishi Uthman, Higgins James D, Henderson Ian R, Edwards Keith J, Franklin F Chris H, Sanchez-Moran Eugenio
School of Biosciences, University of Birmingham, Birmingham, United Kingdom.
Department of Genetics and Genome Biology, University of Leicester, Leicester, United Kingdom.
Front Plant Sci. 2021 Feb 12;12:631323. doi: 10.3389/fpls.2021.631323. eCollection 2021.
Meiotic recombination generates genetic variation and provides physical links between homologous chromosomes (crossovers) essential for accurate segregation. In cereals the distribution of crossovers, cytologically evident as chiasmata, is biased toward the distal regions of chromosomes. This creates a bottleneck for plant breeders in the development of varieties with improved agronomic traits, as genes situated in the interstitial and centromere proximal regions of chromosomes rarely recombine. Recent advances in wheat genomics and genome engineering combined with well-developed wheat cytogenetics offer new opportunities to manipulate recombination and unlock genetic variation. As a basis for these investigations we have carried out a detailed analysis of meiotic progression in hexaploid wheat () using immunolocalization of chromosome axis, synaptonemal complex and recombination proteins. 5-Bromo-2'-deoxyuridine (BrdU) labeling was used to determine the chronology of key events in relation to DNA replication. Axis morphogenesis, synapsis and recombination initiation were found to be spatio-temporally coordinated, beginning in the gene-dense distal chromosomal regions and later occurring in the interstitial/proximal regions. Moreover, meiotic progression in the distal regions was coordinated with the conserved chromatin cycles that are a feature of meiosis. This mirroring of the chiasma bias was also evident in the distribution of the gene-associated histone marks, H3K4me3 and H3K27me3; the repeat-associated mark, H3K27me1; and H3K9me3. We believe that this study provides a cytogenetic framework for functional studies and ongoing initiatives to manipulate recombination in the wheat genome.
减数分裂重组产生遗传变异,并在同源染色体之间提供物理连接(交叉互换),这对于精确分离至关重要。在谷类作物中,交叉互换(细胞学上表现为交叉)的分布偏向于染色体的远端区域。这给植物育种者培育具有改良农艺性状的品种带来了瓶颈,因为位于染色体臂间和着丝粒近端区域的基因很少发生重组。小麦基因组学和基因组工程的最新进展,结合成熟的小麦细胞遗传学,为操纵重组和释放遗传变异提供了新机会。作为这些研究的基础,我们利用染色体轴、联会复合体和重组蛋白的免疫定位,对六倍体小麦()的减数分裂进程进行了详细分析。使用5-溴-2'-脱氧尿苷(BrdU)标记来确定与DNA复制相关的关键事件的时间顺序。发现轴形态发生、联会和重组起始在时空上是协调的,始于基因密集的远端染色体区域,随后发生在臂间/近端区域。此外,远端区域的减数分裂进程与减数分裂特有的保守染色质周期相协调。交叉偏向的这种反映在与基因相关的组蛋白标记H3K4me3和H3K27me3、与重复序列相关的标记H3K27me1以及H3K9me3的分布中也很明显。我们相信这项研究为功能研究以及正在进行的操纵小麦基因组重组的计划提供了细胞遗传学框架。