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从御谷中克隆和鉴定编码细胞质 Hsc70 的基因可能在应对非生物胁迫中发挥保护作用。

Molecular cloning and characterization of gene encoding for cytoplasmic Hsc70 from Pennisetum glaucum may play a protective role against abiotic stresses.

机构信息

International Centre for Genetic Engineering and Biotechnology (ICGEB), Aruna Asaf Ali Marg, New Delhi, India.

出版信息

Mol Genet Genomics. 2010 Mar;283(3):243-54. doi: 10.1007/s00438-010-0518-7. Epub 2010 Feb 2.

Abstract

Molecular chaperones (Hsps) have been shown to facilitate protein folding or assembly under various developmental and adverse environmental conditions. The aim of this study was to unravel a possible role of heat-shock proteins in conferring abiotic stress tolerance to plants. We isolated a cDNA encoding a cytoplasmic Hsp70 (PgHsc70) from Pennisetum glaucum by screening heat-stress cDNA library. PgHsc70 cDNA encoding 649 amino acids represents all conserved signature motifs characteristic of Hsp70s. The predicted molecular model of PgHsc70 protein suggests that the N-terminus ATP-binding region is evolutionarily conserved, in comparison to C-terminus peptide-binding domains. A single intron in ATPase domain coding region of PgHsc70 exhibited a high degree of conservation with respect to its position and phasing among other plant Hsp70 genes. Recombinant PgHsc70 protein purified from E. coli possessed in vitro chaperone activity and protected PgHsc70 expressing bacteria from damage caused by heat and salinity stress. Nucleotide sequence analysis of 5' flanking promoter region of PgHsc70 gene revealed a potential heat-shock element (HSE) and other putative stress-responsive transcription factor binding sites. Positive correlation existed between differentially up-regulated PgHsc70 transcript levels and the duration and intensity of different environmental stresses. Molecular and biochemical analyses revealed that PgHsc70 gene was a member of the Hsp70 family and suggested that its origin was from duplication of a common ancestral gene. Transcript induction data, presence of several putative stress-responsive transcription factor-binding sites in the promoter region of PgHsc70 and the presence of a protective in vitro chaperone activity of this protein against damage caused by heat and salinity, when expressed in E. coli, suggest its probable role in conferring abiotic stress tolerance to this plant.

摘要

分子伴侣(Hsps)已被证明在各种发育和不利的环境条件下促进蛋白质折叠或组装。本研究旨在揭示热休克蛋白在赋予植物非生物胁迫耐受性方面的可能作用。我们通过筛选热应激 cDNA 文库从狼尾草(Pennisetum glaucum)中分离出一个编码细胞质 Hsp70(PgHsc70)的 cDNA。PgHsc70 cDNA 编码 649 个氨基酸,代表 Hsp70 的所有保守特征基序。PgHsc70 蛋白的预测分子模型表明,与 C 末端肽结合结构域相比,N 末端 ATP 结合区域在进化上是保守的。PgHsc70 基因的 ATP 酶结构域编码区中的单个内含子在其位置和相位方面与其他植物 Hsp70 基因高度保守。从大肠杆菌中纯化的重组 PgHsc70 蛋白具有体外伴侣活性,并能保护表达 PgHsc70 的细菌免受热和盐胁迫的损伤。PgHsc70 基因 5'侧翼启动子区的核苷酸序列分析显示出一个潜在的热休克元件(HSE)和其他可能的应激反应转录因子结合位点。差异上调的 PgHsc70 转录物水平与不同环境胁迫的持续时间和强度之间存在正相关。分子和生化分析表明,PgHsc70 基因是 Hsp70 家族的成员,其起源可能是来自共同祖先基因的复制。转录诱导数据、PgHsc70 启动子区存在几个可能的应激反应转录因子结合位点以及该蛋白在大肠杆菌中表达时具有针对热和盐胁迫损伤的保护体外伴侣活性,表明其在赋予该植物非生物胁迫耐受性方面可能发挥作用。

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