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平邑甜茶MhWRKY15基因cDNA克隆及其生物信息学分析

孙晓莉 冉昆 杨洪强 李强 姜倩倩

果树学报2011,Vol.28Issue(6):949-952,4.
果树学报2011,Vol.28Issue(6):949-952,4.

平邑甜茶MhWRKY15基因cDNA克隆及其生物信息学分析

Cloning of MhWRKY15 gene in Malus hupehensis and its bioinformatics analysis

孙晓莉 1冉昆 1杨洪强 1李强 1姜倩倩1

作者信息

  • 1. 山东农业大学园艺科学与工程学院·作物生物学国家重点实验室·山东省果树生物学重点实验室,山东泰安271018
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摘要

Abstract

Full-length cDNA sequence of WRKY15 gene from roots of Malus hupehensis (Pamp.) Rehd. var. pinyiensis Jiang, which was tentatively designated as MhWRKYIS, with GenBank accession number GU576874, was acquired by RT-PCR and RACE with primers designed respectively based on the EST sequence. Bioinformatics analysis indicated that MhWRKY15 was 1 091 bp in length, containing an open reading frame of 810 bp and encoding 269 amino acids, and it belonged to group II of WRKY transcription factors and was one member of WRKY15 family. The results also showed that the protein encoded by MhWRKY15 was a soluble protein, with the molecular formula C_1263H_1941N_365O_425S_12, the relative molecular weight was 29 423.2 ku and the isoelectric point was 5.30. There was one conserved WRKY domain in the protein sequence. The protein might be located in nucleus, and there were many phosphorylation sites, N glycosylation sites and O glycosylation sites. The predicted secondary structure demonstrated that random coil was the most important structural conformation.

关键词

平邑甜茶/WRKY15/cDNA/生物信息学

Key words

Malus hupehensis (Pamp.) Rehd./WRKY15/cDNA/Bioinformatics

分类

农业科技

引用本文复制引用

孙晓莉,冉昆,杨洪强,李强,姜倩倩..平邑甜茶MhWRKY15基因cDNA克隆及其生物信息学分析[J].果树学报,2011,28(6):949-952,4.

基金项目

国家转基因生物新品种培育重大专项(2008ZX08009-3) (2008ZX08009-3)

高校博士点专项科研基金(20103702110003) (20103702110003)

果树学报

OA北大核心CSCDCSTPCD

1009-9980

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