首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Molecular cloning and characterization of the soybean DEAD-box RNA helicase gene induced by low temperature and high salinity stress.
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Molecular cloning and characterization of the soybean DEAD-box RNA helicase gene induced by low temperature and high salinity stress.

机译:低温和高盐度胁迫诱导的大豆DEAD-box RNA解旋酶基因的分子克隆和鉴定。

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摘要

A novel gene encoding a DEAD-box RNA helicase designated as GmRH was isolated from soybean. Amino acid sequence alignment and phylogenetic tree analysis revealed a close relationship between GmRH and other orthologous DEAD-box RNA helicases from other plant species. Structural motif analysis revealed that the bipartite lysine rich nuclear localization signal (NLS) is present in the N-terminal variable region of GmRH and that there are ten conserved motifs found in DEAD-box RNA helicase proteins. Southern blot analysis revealed the presence of 2 copies of GmRH in the soybean genome. Northern blot analysis demonstrated that the RNA expression of the GmRH was induced during low temperature or high salinity stress, but not by the exogenous application of abscisic acid or drought stress. Subcellular localization studies showed that GmRH((1-355))-GFP is localized in the nucleus, whereas GmRH((130-355))-GFP is localized both in the cytoplasm and in the nucleus. This provides the evidence that the N-terminal region predicted as NLS is essential for nuclear targeting of the GmRH protein in the plant cell. Purified GST-GmRH recombinant protein was shown to unwind dsRNA independent of ATP in vitro. Here, we propose that GmRH plays an important role in RNA processing during low temperature and high salinity stresses in plants.
机译:从大豆中分离出编码DEAD-box RNA解旋酶的新基因,命名为GmRH。氨基酸序列比对和系统发育树分析显示,GmRH与其他植物物种的其他直系同源DEAD-box RNA解旋酶之间存在密切关系。结构基序分析显示,富含GyRH的N端可变区存在富含赖氨酸的二聚体核定位信号,并且在DEAD-box RNA解旋酶蛋白中发现了十个保守的基序。 Southern印迹分析显示大豆基因组中存在2个拷贝的GmRH。 Northern印迹分析表明,在低温或高盐度胁迫下诱导了GmRH的RNA表达,但不是通过外源施加脱落酸或干旱胁迫诱导的。亚细胞定位研究表明,GmRH((1-355))-GFP位于细胞核中,而GmRH((130-355))-GFP既位于细胞质中又位于细胞核中。这提供了证据,即预测为NLS的N末端区域对于植物细胞中GmRH蛋白的核靶向至关重要。纯化的GST-GmRH重组蛋白在体外显示出独立于ATP的dsRNA解链作用。在这里,我们建议GmRH在低温和高盐分胁迫下的植物在RNA加工中起重要作用。

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