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ARC3是一种叶绿体分裂因子,是原核生物FtsZ与真核生物磷脂酰肌醇-4-磷酸5-激酶部分的嵌合体。

ARC3, a chloroplast division factor, is a chimera of prokaryotic FtsZ and part of eukaryotic phosphatidylinositol-4-phosphate 5-kinase.

作者信息

Shimada Hiroshi, Koizumi Masato, Kuroki Kouta, Mochizuki Mariko, Fujimoto Hitoshi, Ohta Hiroyuki, Masuda Tatsuru, Takamiya Ken-ichiro

机构信息

Department of Biological Sciences, Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, 4259, Nagatsuta-cho, Midori-ku, Yokohama, Japan.

出版信息

Plant Cell Physiol. 2004 Aug;45(8):960-7. doi: 10.1093/pcp/pch130.

Abstract

The arc3 (accumulation and replication of chloroplast) mutant of Arabidopsis thaliana has a small number of abnormally large chloroplasts in the cell, suggesting that chloroplast division is arrested in the mutant and ARC3 has an important role in the initiation of chloroplast division. To elucidate the role of ARC3, first we identified the ARC3 gene, and determined the location of ARC3 protein during chloroplast division because the localization and spatial orientation of such division factors are vital for correct chloroplast division. Sequencing analysis showed that ARC3 was a fusion of the prokaryotic FtsZ and part of the eukaryotic phosphatidylinositol-4-phosphate 5-kinase (PIP5K) genes. The PIP5K-homologous region of ARC3 had no catalytic domain but a membrane-occupation-and-recognition-nexus (MORN) repeat motif. Immunofluorescence microscopy, Western blotting analysis and in vitro chloroplast import and protease protection assays revealed that ARC3 protein was soluble, and located on the outer surface of the chloroplast in a ring-like structure at the early stage of chloroplast division. Prokaryotes have one FtsZ as a gene for division but have no ARC3 counterparts, the chimera of FtsZ and PIP5K, suggesting that the ARC3 gene might have been generated from FtsZ as another division factor during the evolution of chloroplast by endosymbiosis.

摘要

拟南芥的arc3(叶绿体积累与复制)突变体在细胞中具有少量异常大的叶绿体,这表明该突变体中叶绿体分裂受阻,且ARC3在叶绿体分裂起始过程中具有重要作用。为阐明ARC3的作用,我们首先鉴定了ARC3基因,并确定了ARC3蛋白在叶绿体分裂过程中的定位,因为此类分裂因子的定位和空间取向对于正确的叶绿体分裂至关重要。测序分析表明,ARC3是原核生物FtsZ与真核生物磷脂酰肌醇-4-磷酸5-激酶(PIP5K)基因部分的融合体。ARC3的PIP5K同源区域没有催化结构域,但有一个膜占据与识别连接点(MORN)重复基序。免疫荧光显微镜、蛋白质免疫印迹分析以及体外叶绿体导入和蛋白酶保护试验表明,ARC3蛋白是可溶的,并且在叶绿体分裂早期以环状结构位于叶绿体的外表面。原核生物有一个作为分裂基因的FtsZ,但没有ARC3的对应物,即FtsZ和PIP5K的嵌合体,这表明ARC3基因可能是在叶绿体通过内共生进化过程中从FtsZ作为另一种分裂因子产生的。

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