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谷子胞质I类小热激蛋白基因家族的分子克隆与差异表达

Molecular Cloning and Differential Expression of Cytosolic Class I Small Hsp Gene Family in Pennisetum glaucum (L.).

作者信息

Reddy Palakolanu Sudhakar, Sharma Kiran K, Vadez Vincent, Reddy Malireddy K

机构信息

International Crops Research Institute for the Semi-Arid Tropics (ICRISAT), Patancheru, Hyderabad, 502324, Telangana, India,

出版信息

Appl Biochem Biotechnol. 2015 May;176(2):598-612. doi: 10.1007/s12010-015-1598-y. Epub 2015 Apr 9.

Abstract

Small heat shock protein (Hsp) family genes have been reported in several plant species that function as molecular chaperones to protect proteins from being denatured in extreme conditions. As a first step towards the isolation and characterization of genes that contribute to combating abiotic stresses particularly heat stress, construction and screening of the subtracted complementary DNA (cDNA) library is reported here. In this study, a subtractive heat stress cDNA library was constructed that was used to isolate members of small Hsps (sHsps) using PgsHsp17.9A gene as a probe. As a result, a total of 150 cDNA clones were isolated from the subtracted cDNA library screening, leading to 121 high-quality expressed sequence tags (ESTs), with an average size of 450 bp, comprising of 15 contigs, and majority of these isolated sHsp genes belong to cytosolic class I (CI) family. In silico sequence analysis of CI-sHsp family genes revealed that the length of sHsp proteins varied from 151 to 159 amino acids and showed large variation in isoelectric point value (5.03 to 10.05) and a narrow range of molecular weight (16.09 to 17.94 kDa). The real-time PCR results demonstrated that CI-sHsp genes are differentially expressed in Pennisetum leaves under different abiotic stress conditions particularly at high temperature. The results presented in this study provide basic information on PgCI-sHsp family genes and form the foundation for future functional studies of these genes.

摘要

在几种植物物种中已报道了小热休克蛋白(Hsp)家族基因,它们作为分子伴侣发挥作用,以保护蛋白质在极端条件下不被变性。作为分离和鉴定有助于对抗非生物胁迫特别是热胁迫的基因的第一步,本文报道了消减互补DNA(cDNA)文库的构建和筛选。在本研究中,构建了一个消减热胁迫cDNA文库,该文库用于以PgsHsp17.9A基因作为探针分离小Hsp(sHsp)成员。结果,从消减cDNA文库筛选中总共分离出150个cDNA克隆,得到121个高质量的表达序列标签(EST),平均大小为450 bp,由15个重叠群组成,并且这些分离出的sHsp基因大多数属于胞质I类(CI)家族。对CI-sHsp家族基因的电子序列分析表明,sHsp蛋白的长度在151至159个氨基酸之间变化,等电点值(5.03至10.05)差异较大,分子量范围较窄(16.09至17.94 kDa)。实时PCR结果表明,CI-sHsp基因在狼尾草叶片中在不同非生物胁迫条件下,特别是在高温下差异表达。本研究中呈现的结果提供了关于PgCI-sHsp家族基因的基本信息,并为这些基因未来的功能研究奠定了基础。

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