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青稞脂质转运蛋白基因blt4.9的克隆及其对非生物胁迫的响应

姚晓华 吴昆仑

作物学报2016,Vol.42Issue(3):399-406,8.
作物学报2016,Vol.42Issue(3):399-406,8.DOI:10.3724/SP.J.1006.2016.00399

青稞脂质转运蛋白基因blt4.9的克隆及其对非生物胁迫的响应

Isolation of blt4.9 Gene Encoding LTP Protein in Hulless Barley and Its Re-sponse to Abiotic Stresses

姚晓华 1吴昆仑1

作者信息

  • 1. 青海省农林科学院/ 青海省青稞遗传育种重点实验室/ 青海省高原作物种质资源创新与利用国家重点实验室培育基地,青海西宁810016
  • 折叠

摘要

Abstract

Higher plant lipid transfer protein (LTP) is a class of small molecular weight alkaline single protein that can transfer phospholipids between biomembrane and form the biomembrane in cells. The objective of this study was to understand the func-tion of LTP gene in hulless barley (Hordeum vulgare L. var. nudum Hook. f.). The cDNA sequence of the LTP gene, blt4.9 (Gen-Bank accession number KU170187), was cloned from hulless barley variety Kunlun 12. The full length of blt4.9 cDNA is 720 bp including 348 bp of open reading frame and encodes 115 amino acids. The encoding product is a stable protein with a molecular weight of 11.2 kD, theoretical pI of 9.04, and instability coefficient of 28.41. This protein is rich in Gly, Ala, Leu, and Val amino acids excluding Trp, Glu, and Phe and similar to proteins encoded by other LTP genes. Sequence alignment indicated high simila-rity (98.3%) of protein encoded by blt4.9 from hulless barley and barley (Hordeum vulgare L.). The Real-time PCR assay showed that blt4.9 was up-regulated by 20–30%PEG-6000, 4ºC and 50mmol L-1 ABA and the expression level was higher in the most tolerant variety Handizi than in the most susceptible variety Dama, indicating a possible relationship between stress tolerance and blt4.9 in hulless barley. These results provide basic information in the utilization of LTP genes to improve hulless barley tolerance to abiotic stresses.

关键词

青稞/blt4.9基因/克隆/非生物胁迫/基因表达量

Key words

Hulless barley/blt4.9/Isolation of gene/Abiotic stresses/Gene expression level

引用本文复制引用

姚晓华,吴昆仑..青稞脂质转运蛋白基因blt4.9的克隆及其对非生物胁迫的响应[J].作物学报,2016,42(3):399-406,8.

基金项目

本研究由国家自然科学基金项目(31160284)和国家现代农业产业技术体系建设专项(CARS-05)资助。This study was supported by the National Natural Science Foundation of China (31160284) and the Special Program of Modern Agro-industry Technology System (CARS-05) (31160284)

作物学报

OA北大核心CSCDCSTPCD

0496-3490

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