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Characterization of two genes, Sig1 and Sig2, encoding distinct plastid σ factors1 in the moss Physcomitrella patens: phylogenetic relationships to plastid σ factors in higher plants

机译:苔藓假单胞菌中编码不同质体σ因子的两个基因Sig1和Sig2的特征:高等植物中质体σ因子的系统发育关系

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>We isolated the cDNA for a σ factor from the moss Physcomitrella patens, which possesses unusually large N-terminal extension and the conserved subdomains 1.2–4.2. Phylogenetic analyses indicated that this novel σ factor and PpSIG1* 2, a plastid σ factor previously identified from Physcomitrella, were classified into SigA and SigB groups, two major classes of higher plant plastid σ factors, respectively. According to the nomenclature recently proposed, we renamed PpSIG1* into PpSIG2, and named the novel σ factor PpSIG1. A transient expression assay using a green fluorescent protein showed that the N-terminal region of PpSIG1 acts as a chloroplast-targeting signal. Reverse transcription-PCR experiments showed that light induces the expression of the Sig1 and Sig2 genes encoding PpSIG1 and PpSIG2, respectively. Thus, PpSIG1 and PpSIG2 are likely plastid σ factors regulating plastid gene expression in response to light signals.
机译:>我们从苔藓植物(Physcomitrella patens)中分离了一个具有σ因子的cDNA,该植物具有异常大的N端延伸和保守的1.2-4.2亚结构域。系统发育分析表明,这种新的σ因子和先前从 Physcomitrella 鉴定出的质体σ因子PpSIG1 * 2 分为SigA和SigB组,这是高等植物的两个主要类别质体σ因子分别。根据最近提出的术语,我们将PpSIG1 *重命名为PpSIG2,并命名为新的σ因子PpSIG1。使用绿色荧光蛋白的瞬时表达分析表明,PpSIG1的N端区域充当叶绿体靶向信号。逆转录PCR实验表明,光分别诱导编码PpSIG1和PpSIG2的 Sig1 Sig2 基因的表达。因此,PpSIG1和PpSIG2可能是响应于光信号调节质体基因表达的质体σ因子。

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