Department of Biology and the Integrative Program for Biological and Genome Sciences, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
State Key Laboratory of Genetic Engineering and Collaborative Innovation Center of Genetics and Development, Ministry of Education Key Laboratory of Biodiversity Sciences and Ecological Engineering, Institute of Plant Biology, School of Life Sciences, Fudan University, Shanghai, China.
BMC Genomics. 2021 Mar 12;22(1):181. doi: 10.1186/s12864-021-07497-2.
Meiosis is a specialized cell division that underpins sexual reproduction in most eukaryotes. During meiosis, interhomolog meiotic recombination facilitates accurate chromosome segregation and generates genetic diversity by shuffling parental alleles in the gametes. The frequency of meiotic recombination in Arabidopsis has a U-shaped curve in response to environmental temperature, and is dependent on the Type I, crossover (CO) interference-sensitive pathway. The mechanisms that modulate recombination frequency in response to temperature are not yet known.
In this study, we compare the transcriptomes of thermally-stressed meiotic-stage anthers from msh4 and mus81 mutants that mediate the Type I and Type II meiotic recombination pathways, respectively. We show that heat stress reduces the number of expressed genes regardless of genotype. In addition, msh4 mutants have a distinct gene expression pattern compared to mus81 and wild type controls. Interestingly, ASY1, which encodes a HORMA domain protein that is a component of meiotic chromosome axes, is up-regulated in wild type and mus81 but not in msh4. In addition, SDS the meiosis-specific cyclin-like gene, DMC1 the meiosis-specific recombinase, SYN1/REC8 the meiosis-specific cohesion complex component, and SWI1 which functions in meiotic sister chromatid cohesion are up-regulated in all three genotypes. We also characterize 51 novel, previously unannotated transcripts, and show that their promoter regions are associated with A-rich meiotic recombination hotspot motifs.
Our transcriptomic analysis of msh4 and mus81 mutants enhances our understanding of how the Type I and Type II meiotic CO pathway respond to environmental temperature stress and might provide a strategy to manipulate recombination levels in plants.
减数分裂是一种特殊的细胞分裂,它为大多数真核生物的有性繁殖提供了基础。在减数分裂过程中,同源重组促进了染色体的准确分离,并通过在配子中洗牌亲本等位基因产生遗传多样性。拟南芥减数分裂重组的频率对环境温度呈 U 型曲线,并且依赖于 I 型、交叉(CO)干涉敏感途径。调节重组频率以响应温度的机制尚不清楚。
在这项研究中,我们比较了分别介导 I 型和 II 型减数重组途径的 msh4 和 mus81 突变体热胁迫减数分裂阶段花药的转录组。我们表明,无论基因型如何,热应激都会减少表达基因的数量。此外,msh4 突变体与 mus81 和野生型对照相比具有独特的基因表达模式。有趣的是,编码 HORMA 结构域蛋白的 ASY1 是减数分裂染色体轴的一个组成部分,在野生型和 mus81 中上调,但在 msh4 中没有上调。此外,SDS 是减数特异性细胞周期蛋白样基因,DMC1 是减数特异性重组酶,SYN1/REC8 是减数特异性黏合复合物成分,SWI1 在减数姐妹染色单体黏合中起作用,在所有三种基因型中均上调。我们还描述了 51 个新的、以前未注释的转录本,并表明它们的启动子区域与富含 A 的减数重组热点基序相关。
我们对 msh4 和 mus81 突变体的转录组分析增强了我们对 I 型和 II 型减数 CO 途径如何响应环境温度应激的理解,并可能为操纵植物中的重组水平提供一种策略。