首页 | 本学科首页   官方微博 | 高级检索  
     检索      

水稻(Oryza sativa)新型液泡Na+/H+逆向转运蛋白基因的特征分析和表达
引用本文:刘祝玲,韩胜芳,肖凯.水稻(Oryza sativa)新型液泡Na+/H+逆向转运蛋白基因的特征分析和表达[J].作物学报,2007,33(2):327-332.
作者姓名:刘祝玲  韩胜芳  肖凯
作者单位:1 河北农业大学农学院; 2 河北农业大学生命科学学院, 河北保定071001
摘    要:以拟南芥AtNHX1 cDNA 片段作为探针,筛查水稻盐胁迫植株叶片cDNA 文库,获得与AtNHX1同源的水稻新型液泡Na+/H+逆向转运蛋白基因(OsANT1)。序列分析表明,OsANT1 全长cDNA为2 178 bp,包括一个长度为1 608 bp的完整开放阅读框,编码535个氨基酸残基。在DNA水平上,OsANT1基因含有15个外显子和14个内含子,长度为4 835 bp。OsANT1含有12个跨膜域,系统进化树分析结果表明,与来自拟南芥、水稻、小麦、玉米、大麦、马蔺和芦苇等的Na+/H+逆向转运蛋白高度同源。盐胁迫条件下,OsANT1的表达具有盐分诱导特征,且随着胁迫的增大而增加。表明该基因可能在水稻抵御盐分胁迫的过程中具有一定作用。

关 键 词:水稻(Oryza  sativa  OsANT1  基因特征  基因表达
收稿时间:2006-01-17
修稿时间:1900-01-01

Expression and Characterization of a Novel Vacuole Na+/H+ Antiporter Gene in Rice (Oryza sativa)
Institution:1 College of Agronomy; 2 College of Life Science, Agricultural University of Hebei, Baoding 071001, Hebei, China
Abstract:Using a cDNA fragment PCR amplified from Arabidopsis AtNHX1 as the probe, a novel vacuole Na+/H+ antiporter gene (OsANT1) in rice was obtained based on the screening of a cDNA library made from leaves of rice plants treated with 200 mmol L-1 NaCl. The results indicated that the full-length of OsANT1 cDNA was 2 178 bp. The open reading frame (ORF) of OsANT1 was
1 608 bp with 535 translated amino acids. OsANT1 had 15 exons and 14 introns with a total length of 4 835 bp at the DNA level. It was found that OsANT1 contained 12 transmembrane domains and had high similarities with other vacuole Na+/H+ antiporters from plant species, such as Arabidopsis thaliana, Oryza sativa, Triticum aestivum, Zea mays, Hordeum vulgare, Iris lacteal, and Phragmites australis. The expression of OsANT1 in leaf, stem and root was all induced by NaCl and the expression levels were increased with the increase of NaCl concentration applied and the elongation of NaCl treatment time. Taken together, it is suggested that OsANT1 is functional for rice to withstand NaCl under salt stress.
Keywords:Rice (Oryza sativa)  OsANT1  Gene characterization  Gene expression
点击此处可从《作物学报》浏览原始摘要信息
点击此处可从《作物学报》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号