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水稻OsLEA2基因的克隆及表达分析
利用RT-PCR技术从水稻中克隆到OsLEA2的eDNA。序列分析表明,OsLEA2基因的读码框为312bp,编码一个由103个氨基酸残基组成的蛋白,富含Ala、Lys、Glu、Hjs、Val和衄,不含Asn、Cys、Phe和TW。OsLEA2蛋白的1-73位氨基酸残基形成LEA_I结构域。OsLEA2蛋白的二级结构有3个Ⅱ·螺旋构象区域,没有伸展的B-片层构象,为亲水蛋白。进化树分析表明OsLEA2属于第4组LEA蛋白的4A亚组,OsLEA2与4A亚组LEA蛋白的氨基酸一致性为29%-45%。实时定量liT-PCR分析表明表明OsLEA2基因在水稻的不同生长发育时期的不同组织中都能表达,在完...
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Published in | 西南农业学报 Vol. 25; no. 3; pp. 743 - 749 |
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Main Author | |
Format | Journal Article |
Language | Chinese |
Published |
重庆三峡学院生命科学与工程学院,重庆,404000
2012
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Subjects | |
Online Access | Get full text |
ISSN | 1001-4829 |
DOI | 10.3969/j.issn.1001-4829.2012.03.001 |
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Summary: | 利用RT-PCR技术从水稻中克隆到OsLEA2的eDNA。序列分析表明,OsLEA2基因的读码框为312bp,编码一个由103个氨基酸残基组成的蛋白,富含Ala、Lys、Glu、Hjs、Val和衄,不含Asn、Cys、Phe和TW。OsLEA2蛋白的1-73位氨基酸残基形成LEA_I结构域。OsLEA2蛋白的二级结构有3个Ⅱ·螺旋构象区域,没有伸展的B-片层构象,为亲水蛋白。进化树分析表明OsLEA2属于第4组LEA蛋白的4A亚组,OsLEA2与4A亚组LEA蛋白的氨基酸一致性为29%-45%。实时定量liT-PCR分析表明表明OsLEA2基因在水稻的不同生长发育时期的不同组织中都能表达,在完熟期的根和穗中,OsLEA2基因的表达明显升高。 |
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Bibliography: | HU Ting-zhang, WU Ying-mei, YANG Jun-nian, WU Xiao-li (School of Life Science and Engineering, Chongqing Three Gorges University, Chongqing 404000, China) 51-1213/S The cDNA sequence of OsLEA2 from rice was cloned and analyzed by RT-PCR. The results showed that OsLEA2 contained a 312 bp ORF encoding a putative polypeptide of 103 amino acids, which was rich in Ala, Lys, Glu, His, Val and Arg, and lacking in Asu, Cys, Pbe and Trp residues. OsLEA2 protein contained a Pfam:LEA_I domain architecture at position 1 -73 with three a-helical domains and without {5-sheet domain, and was strongly hydrophilic. The phylogenetic relationship between related group 4 LEA proteins from different plants was analyzed, which showed that OsLEA2 belonged to subgroup 4A. The amino acid sequence of OsLEA2 showed 29 % -45 % se- quence identity with other members of subgroup 4A LEA proteins from plants. Real-time RT-PCR analysis revealed that OsLEA2 could ex- press in different tissue organ during different development stages of rice. I |
ISSN: | 1001-4829 |
DOI: | 10.3969/j.issn.1001-4829.2012.03.001 |