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两个拟南芥叶绿体GrpE同源物具有不同的生物学活性,且能形成同型和异型寡聚体。

Two Arabidopsis Chloroplast GrpE Homologues Exhibit Distinct Biological Activities and Can Form Homo- and Hetero-Oligomers.

作者信息

Su Pai-Hsiang, Lin Hsuan-Yu, Lai Yen-Hsun

机构信息

Agricultural Biotechnology Research Center, Academia Sinica, Taipei, Taiwan.

Biotechnology Center in Southern Taiwan, Academia Sinica, Tainan, Taiwan.

出版信息

Front Plant Sci. 2020 Jan 22;10:1719. doi: 10.3389/fpls.2019.01719. eCollection 2019.

Abstract

Flowering plants have evolved two distinct clades of chloroplast GrpE homologues (CGEs), which are the nucleotide exchange factor for Hsp70. In Arabidopsis, they are named AtCGE1 (At5g17710) and AtCGE2 (At1g36390). Characterization of their corresponding T-DNA insertion mutants revealed that there is no visible change in phenotype except a defect in protein import in an -knockout mutant under normal growth conditions. However, the embryo development of an -knockout mutant was arrested early at the globular stage. An -knockdown mutant, harboring a T-DNA insertion in the 5'-UTR region, exhibited growth retardation and protein import defect, and its mutant phenotypes became more severe when was further knocked out. Sub-organellar distribution implied that AtCGE2 might be important for membrane biology due to its preferential association with chloroplast membranes. Biochemical studies and complementation tests showed that only AtCGE1, but not AtCGE2, can effectively rescue the heat-sensitive phenotype of mutant and robustly stimulate the refolding of denatured luciferase by DnaK. Interestingly, AtCGE1 and AtCGE2 are tending to form heterocomplexes, which exhibit comparable co-chaperone activity to AtCGE1 homocomplexes. Our data indicate that AtCGE1 is the principle functional homologue of GrpE. The possibility that AtCGE2 has a subsidiary or regulatory function through homo- and/or hetero-oligomerization is discussed.

摘要

开花植物进化出了两个不同的叶绿体GrpE同源物(CGEs)分支,它们是Hsp70的核苷酸交换因子。在拟南芥中,它们被命名为AtCGE1(At5g17710)和AtCGE2(At1g36390)。对其相应的T-DNA插入突变体的表征显示,在正常生长条件下,除了一个敲除突变体中蛋白质导入存在缺陷外,表型没有明显变化。然而,一个敲除突变体的胚胎发育在球形期早期就停止了。一个在5'-UTR区域有T-DNA插入的敲低突变体表现出生长迟缓以及蛋白质导入缺陷,当进一步敲除AtCGE2时,其突变表型变得更加严重。亚细胞器分布表明,AtCGE2可能因其与叶绿体膜的优先结合而对膜生物学很重要。生化研究和互补试验表明,只有AtCGE1,而不是AtCGE2,能够有效挽救突变体的热敏感表型,并有力地刺激DnaK对变性荧光素酶的重折叠。有趣的是,AtCGE1和AtCGE2倾向于形成异源复合物,其共伴侣活性与AtCGE1同源复合物相当。我们的数据表明,AtCGE1是GrpE的主要功能同源物。文中还讨论了AtCGE2通过同聚和/或异聚具有辅助或调节功能的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6085/6987454/d5a2b89f7591/fpls-10-01719-g001.jpg

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