Mu Na, Li Yafei, Li Sanhe, Shi Wenqing, Shen Yi, Yang Han, Zhang Fanfan, Tang Ding, Du Guijie, You Aiqing, Cheng Zhukuan
Jiangsu Co-Innovation Center for Modern Production Technology of Grain Crops, Yangzhou University, 225009, Yangzhou, China.
State Key Lab of Plant Genomics, Institute of Genetics and Developmental Biology, Innovation Academy for Seed Design, Chinese Academy of Sciences, 100101, Beijing, China.
New Phytol. 2023 Mar;237(6):2422-2434. doi: 10.1111/nph.18668. Epub 2022 Dec 26.
The endonuclease methyl methanesulfonate and UV-sensitive protein 81 (MUS81) has been reported to participate in DNA repair during mitosis and meiosis. However, the exact meiotic function of MUS81 in rice remains unclear. Here, we use a combination of physiological, cytological, and genetic approaches to provide evidence that MUS81 functions in atypical recombination intermediate resolution rather than crossover designation in rice. Cytological and genetic analysis revealed that the total chiasma numbers in mus81 mutants were indistinguishable from wild-type. The numbers of HEI10 foci (the sites of interference-sensitive crossovers) in mus81 were also similar to that of wild-type. Moreover, disruption of MUS81 in msh5 or msh4 msh5 background did not further decrease chiasmata frequency, suggesting that rice MUS81 did not function in crossover designation. Mutation of FANCM and ZEP1 could enhance recombination frequency. Unexpectedly, chromosome fragments and bridges were frequently observed in mus81 zep1 and mus81 fancm, illustrating that MUS81 may resolve atypical recombination intermediates. Taken together, our data suggest that MUS81 contributes little to crossover designation but plays a crucial role in the resolution of atypical meiotic intermediates by working together with other anti-crossover factors.
据报道,核酸内切酶甲磺酸甲酯和紫外线敏感蛋白81(MUS81)参与有丝分裂和减数分裂过程中的DNA修复。然而,MUS81在水稻减数分裂中的具体功能仍不清楚。在这里,我们结合生理、细胞学和遗传学方法,提供证据表明MUS81在水稻中发挥作用于非典型重组中间体的解析,而不是交叉指定。细胞学和遗传学分析表明,mus81突变体中的总交叉数与野生型没有区别。mus81中HEI10焦点(干扰敏感交叉的位点)的数量也与野生型相似。此外,在msh5或msh4 msh5背景中破坏MUS81并没有进一步降低交叉频率,这表明水稻MUS81在交叉指定中不起作用。FANCM和ZEP1的突变可以提高重组频率。出乎意料的是,在mus81 zep1和mus81 fancm中经常观察到染色体片段和桥,说明MUS81可能解析非典型重组中间体。综上所述,我们的数据表明MUS81对交叉指定贡献不大,但通过与其他抗交叉因子协同作用,在非典型减数分裂中间体的解析中起关键作用。