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拟南芥中线粒体靶向单链DNA结合蛋白的特性分析

Characterization of a mitochondrially targeted single-stranded DNA-binding protein in Arabidopsis thaliana.

作者信息

Edmondson Andrew C, Song Daqing, Alvarez Luis A, Wall Melisa K, Almond David, McClellan David A, Maxwell Anthony, Nielsen Brent L

机构信息

Department of Microbiology and Molecular Biology, Brigham Young University, 775 WIDB, Provo, UT, 84602, USA.

出版信息

Mol Genet Genomics. 2005 Apr;273(2):115-22. doi: 10.1007/s00438-004-1106-5. Epub 2005 Mar 3.

Abstract

A gene encoding a predicted mitochondrially targeted single-stranded DNA binding protein (mtSSB) was identified in the Arabidopsis thaliana genome sequence. This gene (At4g11060) codes for a protein of 201 amino acids, including a 28-residue putative mitochondrial targeting transit peptide. Protein sequence alignment shows high similarity between the mtSSB protein and single-stranded DNA binding proteins (SSB) from bacteria, including residues conserved for SSB function. Phylogenetic analysis indicates a close relationship between this protein and other mitochondrially targeted SSB proteins. The predicted targeting sequence was fused with the GFP coding region, and the organellar localization of the expressed fusion protein was determined. Specific targeting to mitochondria was observed in in-vitro import experiments and by transient expression of a GFP fusion construct in Arabidopsis leaves after microprojectile bombardment. The mature mtSSB coding region was overexpressed in Escherichia coli and the protein was purified for biochemical characterization. The purified protein binds single-stranded, but not double-stranded, DNA. MtSSB stimulates the homologous strand-exchange activity of E. coli RecA. These results indicate that mtSSB is a functional homologue of the E. coli SSB, and that it may play a role in mitochondrial DNA recombination.

摘要

在拟南芥基因组序列中鉴定出一个编码预测的线粒体靶向单链DNA结合蛋白(mtSSB)的基因。该基因(At4g11060)编码一个由201个氨基酸组成的蛋白质,包括一个28个残基的假定线粒体靶向转运肽。蛋白质序列比对显示mtSSB蛋白与细菌的单链DNA结合蛋白(SSB)高度相似,包括保守的SSB功能残基。系统发育分析表明该蛋白与其他线粒体靶向的SSB蛋白关系密切。将预测的靶向序列与GFP编码区融合,并确定表达的融合蛋白的细胞器定位。在体外导入实验以及通过微弹轰击后在拟南芥叶片中瞬时表达GFP融合构建体,观察到该蛋白特异性靶向线粒体。成熟的mtSSB编码区在大肠杆菌中过表达,并纯化该蛋白用于生化特性分析。纯化的蛋白结合单链DNA,但不结合双链DNA。MtSSB刺激大肠杆菌RecA的同源链交换活性。这些结果表明mtSSB是大肠杆菌SSB的功能同源物,并且它可能在线粒体DNA重组中起作用。

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