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来自小立碗藓的质体sigma因子cDNA的克隆与特性分析

Cloning and characterization of the cDNA for a plastid sigma factor from the moss Physcomitrella patens.

作者信息

Hara K, Sugita M, Aoki S

机构信息

Division of Biological Informatics, Graduate School of Human Informatics, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8601, Japan.

出版信息

Biochim Biophys Acta. 2001 Jan 26;1517(2):302-6. doi: 10.1016/s0167-4781(00)00250-5.

Abstract

We isolated a cDNA PpSig1 encoding a plastid sigma factor from the moss Physcomitrella patens. The PpSIG1 protein is composed of the conserved subdomains for recognition of -10 and -35 promoter elements, core complex binding and DNA melting. Southern blot analysis showed that the moss sig1 gene is likely a member of a small gene family. Transient expression assay using green fluorescent protein demonstrated that the N-terminal region of PpSIG1 functions as a chloroplast-targeting signal peptide. These observations suggest that multiple nuclear-encoded sigma factors regulate chloroplast gene expression in P. patens.

摘要

我们从苔藓小立碗藓中分离出一个编码质体sigma因子的cDNA PpSig1。PpSIG1蛋白由用于识别-10和-35启动子元件、核心复合体结合和DNA解链的保守亚结构域组成。Southern杂交分析表明,苔藓sig1基因可能是一个小基因家族的成员。使用绿色荧光蛋白的瞬时表达试验表明,PpSIG1的N端区域作为叶绿体靶向信号肽发挥作用。这些观察结果表明,多个核编码的sigma因子调节小立碗藓中的叶绿体基因表达。

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