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林业科学 ›› 2012, Vol. 48 ›› Issue (10): 41-48.doi: 10.11707/j.1001-7488.20121008

• 论文 • 上一篇    下一篇

巨桉EgrCBF 1 EgrCBF 2 基因的克隆和胁迫响应表达分析

王京京, 童再康, 黄程前, 程龙军   

  1. 浙江农林大学 亚热带森林培育国家重点实验室培育基地 临安 311300
  • 收稿日期:2012-02-17 修回日期:2012-03-19 出版日期:2012-10-25 发布日期:2012-10-25
  • 通讯作者: 程龙军

Cloning of EgrCBF 1 and EgrCBF 2 Genes from Eucalyptus grandis and their Expression under Stresses

Wang Jingjing, Tong Zaikang, Huang Chengqian, Cheng Longjun   

  1. The Nurturing Station for the State Key Laboratory of Subtropical Silviculture Zhejiang A & F University Lin'an 311300
  • Received:2012-02-17 Revised:2012-03-19 Online:2012-10-25 Published:2012-10-25

摘要:

从低温诱导的巨桉幼苗中克隆到2条CBF的全长cDNA序列,命名为EgrCBF 1EgrCBF 2 ,全长分别为1 062 bp和1 203 bp,编码220个氨基酸和196个氨基酸,命名为EgrCBF 1EgrCBF 2 (GenBank登录号分别为: JQ068827; JQ068828),都包含1个AP2结构域。2个基因编码的蛋白都与冈尼桉中CBF蛋白(DQ241820)具有很高的同源性,与EguCBF1a的同源性分别达到了91%和80%。RT-PCR分析表明,EgrCBF 1 主要在叶和根中表达,而EgrCBF 2 在叶、茎和根中都有表达。对不同低温条件(0,2,4,6,8 ℃)和4 ℃ 2,4,8,24,48 h处理下EgrCBF 1EgrCBF 2 的qRT-PCR分析表明: 2个基因都受低温诱导,并在2 ℃时诱导水平达到最高; 4 ℃下随低温时间的延长,它们的诱导表达特性都呈先升后降的趋势。在100 μmol·L-1 ABA,200 mmol·L-1 NaCl和干旱处理下,EgrCBF 1 受ABA和干旱诱导,EgrCBF 2 则受干旱和高盐胁迫诱导。

关键词: 巨桉, CBF, 冷, ABA, 干旱, 高盐

Abstract:

Two CBF genes named EgrCBF 1 and EgrCBF 2 (GenBank No. JQ068827; JQ068828)were isolated from Eucalyptus grandis seedlings under low temperature. Sequence analysis showed that EgrCBF 1 and EgrCBF 2 cDNA had 1 062 bp and 1 203 bp, respectively. The two genes encoded 220 and 196 amino acids, separately and both contained an AP2 domain. The results of homology comparison showed that EgrCBF1 and EgrCBF2 protein shared 91% and 80% homology with EguCBF 1 a. Spatial expression analyses showed that EgrCBF 1 expressed mainly in leaves and roots while EgrCBF 2 expressed in all leaves, stems and roots. qRT-PCR result of EgrCBF 1 and EgrCBF 2 under 0 ℃,2 ℃,4 ℃,6 ℃,and 8 ℃ revealed that they were both induced by low temperatures and reached the highest level at 2 ℃. Time course of the genes expressions at 4 ℃ for 2 h,4 h,8 h,24 h,and 48 h showed that their expressions increased at the first and then decreased. Changes in EgrCBF 1 and EgrCBF 2 expression under 100 μmol·L-1ABA, 200 mmol·L-1NaCl and drought were also analyzed. The results showed EgrCBF 1 was up-regulated under drought stress and ABA treatment, while the expression of EgrCBF 2 increased under drought and salt stress.

Key words: Eucalyptus grandis, CBF, cold, ABA, drought, salt

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