[Cloning and expression in E.coli of Chlamydomonas reinhardtii CrFtsZ3 gene].

Yong Hu, Dong-Dong Kong, Dong Wang, Yi-Kun He
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Abstract

FtsZ protein plays a key role in the division of bacteria and chloroplast. To investigate the evolution of the chloroplast dividing apparatus, cloning and molecular characterization of a second chloroplast division gene, CrFtsZ3, from Chlamydomonas reinhardtii is performed. As there are two ftsZ genes in Chlamydomonas reinhardtii, duplication and divergence of the ftsZ genes might occur in an early stage before the emergence of green algae during the course of plant evolution. Sequence analysis showed that CrFtsZ3 gene had significant sequence homology with other ftsZs. It encoded a precursor of 479 amino acid residues with a putative transit peptide in its N-terminal. To study the function of CrFtsZ3, a recombinant plasmid expressing the full length CrFtsZ3/EGFP fusion protein was constructed. By using IPTG inducing, overexpression of CrFtsZ3/EGFP in E.coli was achieved, and this overexpression blocked cell division and resulted in filament formation. GFP-derived fluorescence showed regularly spaced dots along the bacterial filaments. This suggests that CrFtsZ3 could still recognize the signals of cell division site in E.coli and could take part in the process of bacterial division.

莱茵衣藻CrFtsZ3基因的克隆及在大肠杆菌中的表达
FtsZ蛋白在细菌和叶绿体的分裂中起关键作用。为了研究莱茵衣藻叶绿体分裂器的进化过程,对衣藻叶绿体分裂第二基因CrFtsZ3的克隆和分子特征进行了研究。由于莱茵衣藻中存在两个ftsZ基因,在植物进化过程中,ftsZ基因的复制和分化可能早在绿藻出现之前就已经发生了。序列分析表明,CrFtsZ3基因与其他ftsZs基因序列具有显著的同源性。它编码了479个氨基酸残基的前体,在其n端有一个假定的传递肽。为了研究CrFtsZ3的功能,构建了表达CrFtsZ3/EGFP全长融合蛋白的重组质粒。通过IPTG诱导,在大肠杆菌中实现了CrFtsZ3/EGFP的过表达,这种过表达阻断了细胞分裂,导致了纤维的形成。gfp衍生的荧光显示沿细菌细丝有规则间隔的点。这说明CrFtsZ3在大肠杆菌中仍能识别细胞分裂位点的信号,并能参与细菌分裂过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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