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来自沙冬青的磷脂酶Dα基因的过表达增强了磷脂酶Dα1缺陷型拟南芥突变体的耐盐性。

Overexpression of a phospholipase Dα gene from Ammopiptanthus nanus enhances salt tolerance of phospholipase Dα1-deficient Arabidopsis mutant.

作者信息

Yu Hao Qiang, Yong Tai Ming, Li Hong Jie, Liu Yan Ping, Zhou Shu Feng, Fu Feng Ling, Li Wan Chen

机构信息

Maize Research Institute, Sichuan Agricultural University, Chengdu, 611130, Sichuan, People's Republic of China.

Faculty of Plant Science, Tarim University, Alar, 843300, Xinjiang, People's Republic of China.

出版信息

Planta. 2015 Dec;242(6):1495-509. doi: 10.1007/s00425-015-2390-5. Epub 2015 Aug 30.

Abstract

A phospholipase Dα gene ( AnPLDα ) was cloned from xerophytic desert plant Ammopiptanthus nanus and its overexpression enhanced salt tolerance of a PLDα1 deficient Arabidopsis mutant. Phospholipase Dα (PLDα) hydrolyzes phosphatidylcholine to produce phosphatidic acid, and plays crucial role in plant tolerance to abiotic stress. In this study, a phospholipase Dα gene (AnPLDα) was cloned from xerophyte Ammopiptanthus nanus by the methods of homologous cloning and rapid amplification of cDNA ends, and evaluated for its function in stress tolerance. The full-length cDNA was 2832 bp long, containing an open reading frame of 2427 bp that encodes 808 amino acids. The putative protein was predicted to be localized to the cytoplasm and this was confirmed by transient expression of a fluorescent fusion protein. The endogenous expression of the AnPLDα gene was induced by high salt, dehydration, cold and abscisic acid. The heterologous expression of the AnPLDα gene improved salt tolerance of an Arabidopsis pldα1 knocked out mutant, and positively regulated the expression of the AtABI, AtNCED, AtRD29A, AtRD29B and AtADH genes. Therefore, the AnPLDα gene was concluded to be involved in response to abiotic stress. The AnPLDα gene is a hopeful candidate for transgenic application to improve stress tolerance of commercial crops.

摘要

从旱生沙漠植物膜荚黄芪中克隆了一个磷脂酶Dα基因(AnPLDα),其过表达增强了磷脂酶Dα1缺陷型拟南芥突变体的耐盐性。磷脂酶Dα(PLDα)水解磷脂酰胆碱生成磷脂酸,在植物对非生物胁迫的耐受性中起关键作用。本研究通过同源克隆和cDNA末端快速扩增方法从旱生植物膜荚黄芪中克隆了一个磷脂酶Dα基因(AnPLDα),并对其在胁迫耐受性中的功能进行了评估。全长cDNA长2832 bp,包含一个2427 bp的开放阅读框,编码808个氨基酸。预测该推定蛋白定位于细胞质,荧光融合蛋白的瞬时表达证实了这一点。AnPLDα基因的内源表达受高盐、脱水、低温和脱落酸诱导。AnPLDα基因的异源表达提高了拟南芥pldα1敲除突变体的耐盐性,并正向调节AtABI、AtNCED、AtRD29A、AtRD29B和AtADH基因的表达。因此,得出结论AnPLDα基因参与非生物胁迫响应。AnPLDα基因是转基因应用以提高商业作物胁迫耐受性的一个有希望的候选基因。

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