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MSH7 错配修复蛋白在拟南芥适应急性盐胁迫中的作用。

Role of the mismatch repair protein MSH7 in Arabidopsis adaptation to acute salt stress.

机构信息

Centro de Estudios Fotosintéticos y Bioquímicos (CEFOBI), Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Suipacha 531, 2000, Rosario, Argentina.

Centro de Estudios Fotosintéticos y Bioquímicos (CEFOBI), Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Suipacha 531, 2000, Rosario, Argentina.

出版信息

Plant Physiol Biochem. 2021 Dec;169:280-290. doi: 10.1016/j.plaphy.2021.11.029. Epub 2021 Nov 19.

Abstract

DNA mismatch repair (MMR) is a highly conserved pathway in evolution responsible for maintaining genomic stability. MMR is initiated when MutS proteins recognize and repair single base-base mismatches and small loops of unpaired nucleotides as well as certain types of DNA damage. Arabidopsis thaliana and other plants contain MutS protein homologs (MSH) found in other eukaryotic organisms and a unique MSH7 polypeptide. In this study, we first evaluated transient expression profiles of ten-days old pAtMSH7:GUS transgenic seedlings at different recovery times after an acute treatment for 48 hs with100 mM NaCl. GUS histochemical staining indicated that MSH7 expression is repressed by salt exposure but recovers progressively. Then, ten-days old mutants harboring two independent msh7 alleles were exposed for 48 hs with100 mM NaCl and different traits were measured over recovery time. Salt treated msh7 seedlings were defective in G2/M arrest. As a result, msh7 seedlings showed a reduced salt inhibitory effect as evidenced by a decreased reduction of rosette and leaf areas, stomatal density, total leaf number, silique length and seed number per silique. These findings suggest that disruption of MSH7 activity could be a promising approach for plant adaptive responses to salinity stress.

摘要

DNA 错配修复(MMR)是进化中高度保守的途径,负责维持基因组稳定性。当 MutS 蛋白识别并修复单碱基对错配和未配对核苷酸的小环以及某些类型的 DNA 损伤时,MMR 就会启动。拟南芥和其他植物含有在其他真核生物中发现的 MutS 蛋白同源物(MSH)和独特的 MSH7 多肽。在这项研究中,我们首先评估了在急性 48 小时 100mM NaCl 处理后不同恢复时间的 10 天大的 pAtMSH7:GUS 转基因幼苗的瞬时表达谱。GUS 组织化学染色表明,MSH7 表达受盐暴露抑制,但逐渐恢复。然后,将含有两个独立 msh7 等位基因的 10 天大的突变体暴露于 100mM NaCl 中 48 小时,并在恢复时间内测量不同的特征。盐处理的 msh7 幼苗在 G2/M 期停滞中出现缺陷。结果,msh7 幼苗的盐抑制作用降低,表现在减少的莲座叶和叶片面积、气孔密度、总叶片数、蒴果长度和每个蒴果的种子数减少。这些发现表明,破坏 MSH7 活性可能是植物适应盐胁迫的一种有前途的方法。

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