首页|甘蔗CIPK 23基因克隆及对低钾、干旱、盐胁迫的响应

甘蔗CIPK 23基因克隆及对低钾、干旱、盐胁迫的响应

扫码查看
本研究采用RT-PCR技术从低钾胁迫的甘蔗根系中克隆得到一个长度为1749 bp的与CBL互作的丝氨酸/苏氨酸蛋白激酶基因,命名为SsCIPK23(GenBank登录号为KM981737),包含1350 bp的开放阅读框(ORF),可编码一个449氨基酸残基的多肽。SsCIPK23具有CIPK基因家族典型的蛋白激酶结构域和NAF调控结构域。进化树分析显示SsCIPK23与其他作物的CIPK23关系较近,具有较高的保守性。qPCR分析结果表明,在低钾、干旱和盐胁迫下,SsCIPK23的表达都发生改变。在低钾胁迫24 h后SsCIPK23相对表达量开始上升,而且随着胁迫时间的延长,相对表达量持续增加;而在干旱和盐胁迫下,相对表达量最高出现在48 h,随后表达量开始下降,暗示了该基因在低钾、干旱和盐胁迫下发挥重要的调控作用,可为深入研究SsCIPK23基因功能奠定坚实的基础。
Molecular Cloning and Expression Analysis of CIPK 23 Gene from Sugarcane under Low Potassium, Drought and Salt Stress
In this study, A CBL-interacting protein kinase gene named SsCIPK23 (GenBank accession number:KM981737) was cloned by reverse transcription-polymerase chain reaction (RT-PCR) from root of sugarcane und-er low potassium stress. The full length of SsCIPK23 gene was 1 749 bp, containing a 1 350 bp complete open reading frame, which encoded 449 amino acids. The SsCIPK23 contained a protein kinase and a NAF domain which are the typical domains of CIPK family. The phylogenetic analysis of SsCIPK23 with CIPK family in various plants revealed that SsCIPK23 was closely related with CIPK23 of various plants and the CIPK23 genes in various plants were highly conservative. The result of qPCR indicated that the expression of SsCIPK23 was changed with low potassium, drought and salt stresses. Under low potassium stress, the expression of SsCIPK23 was up-regulated at 24 h under, and the relative expression increased with the stress time;under drought and salt stress, the highest relative express of SsCIPK23 appeared at 48 h and then relative express decreased at 92 h. The results revealed that the SsCIPK23 might take part in responses to various stress. It builds a great base for researching functional of SsCIPK23.

SugarcaneCIPK 23 geneLow potassium StressDrought stressSalt stress

凌秋平、曾巧英、胡斐、陈健文、吴嘉云、李奇伟、齐永文

展开 >

广东省甘蔗改良与生物炼制重点实验室,广州甘蔗糖业研究所,广州,510316

甘蔗 CIPK 23基因 低钾胁迫 干旱胁迫 盐胁迫

国家甘蔗产业技术体系国家自然科学基金广东省科技计划广东省科技计划

CARS-20-1-4312012592012A0614000052012A090300015

2015

分子植物育种
海南省生物工程协会

分子植物育种

CSTPCDCSCD北大核心
影响因子:0.765
ISSN:1672-416X
年,卷(期):2015.(6)
  • 18
  • 3