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通过cDNARDA法分离和识别盐藻(Dunaliella salina)盐胁迫相关基因
引用本文:方孝东,黄薇,林栖凤,李冠一,屈良鹄.通过cDNARDA法分离和识别盐藻(Dunaliella salina)盐胁迫相关基因[J].中国生物化学与分子生物学报,2004,20(1):67-72.
作者姓名:方孝东  黄薇  林栖凤  李冠一  屈良鹄
作者单位:1. 基因工程教育部重点实验室,中山大学生物工程研究中心,广州,510275;海南省耐盐作物生物技术重点实验室,海南大学生物科学技术研究所,海口,570228
2. 海南省耐盐作物生物技术重点实验室,海南大学生物科学技术研究所,海口,570228;西安交通大学生命科学与技术学院,西安,710049
3. 海南省耐盐作物生物技术重点实验室,海南大学生物科学技术研究所,海口,570228
4. 基因工程教育部重点实验室,中山大学生物工程研究中心,广州,510275
基金项目:国家教育部重点项目 ( 0 2 165 ),海南省自然科学基金 ( 3 0 0 0 9),国家“九五”重点科技攻关项目 ( 85 72 2 2 7 0 1),国家科技部项目基金 (J0 0 A 0 0 9)资助项目~~
摘    要:采用cDNA代表性差异分析 (RDA)技术 ,对盐藻在盐胁迫时差异表达的基因进行了分离鉴定 .在分离到的 10个基因中 ,有 5个与已知基因同源 (包括叶绿素a b结合蛋白基因、蛋白磷酸酶I催化亚基基因和 3个核糖体蛋白基因 ) ,还有 5个未知功能基因则是首次在盐藻中被分离 .值得注意的是 ,所有这 5个已知基因的功能都与细胞分裂或盐胁迫有关 .结果表明 :取样时盐藻细胞仍处于恢复阶段 ,所分离到的基因对于盐藻耐盐可能具有重要意义 ;蛋白磷酸酶I的下调表达可能是盐藻调节离子平衡的一个重要过程和细胞分裂受阻的原因所在 ;盐藻减缓细胞分裂速度可能是为了减少能量消耗 ,以留出足够的能量来应对盐胁迫 ;其它 5个未知基因可能也与盐藻适应盐胁迫机制有关 .

关 键 词:盐藻  盐胁迫  差异表达  基因分离鉴定  代表性差异分析  
收稿时间:2004-02-20
修稿时间:2003年2月25日

Isolation and Identification of Genes Involved in Salt-Adaptation of Dunaliella salina by cDNA RDA
FANG Xiao-dong,HUANG Wei,LIN Qi-feng ,LI Guan-yi ,QU Liang-hu.Isolation and Identification of Genes Involved in Salt-Adaptation of Dunaliella salina by cDNA RDA[J].Chinese Journal of Biochemistry and Molecular Biology,2004,20(1):67-72.
Authors:FANG Xiao-dong    HUANG Wei    LIN Qi-feng  LI Guan-yi  QU Liang-hu
Institution:( 1) Key Laboratory of Gene Engineering of Ministry of Education, Biotechnology Research Center, Zhongshan University, Guangzhou 510275, China; 2) Hainan Provincial Key Laboratory of Biotechnology for Salt-tolerance Crops, Institute of Biological Science and Technology, Hainan University, Haikou 570228, China; 3)Institute of Life Science and Technology, Xi′an Jiaotong University, Xi′an 710049, Shanxi, China
Abstract:Representational difference analysis of cDNA (cDNA RDA) has been performed to isolate the genes involved in salt-adaptation of D. salina. 11 differentially expressed clones were isolated. Among 10 sequences precisely determined from the clones, 5 sequences were homologues to known genes of other organisms, but the other 5 sequences with unknown function were identified for the first time. Remarkably, all of the 5 known genes, including 3 ribosomal protein genes, PP1 gene, and chlorophyll a/b binding protein gene, are either cell proliferation related or salt-tolerance related. It is suggested that D. salina cells are still in the process of recovering from salt stress at the time of sampling, and the isolated genes might be of importance for salt tolerance of D. salina. The decreased expression of PP1 gene might be an important process of ion homeostasis regulation for D. salina adapting to hyperosmotic shock, and the cause for the suppression of cell proliferation. The possible reason for the slowed proliferation rate of D. salina cell might be to reduce energy consumption to leave more energy to conquer salt stress. The other 5 unknown genes might be involved in salt-adaptation of D. salina also.
Keywords:Dunaliella salina  salt stress  differential expression  gene identification  cDNA RDA
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