水稻OsPIN1b基因GFP融合表达载体构建及转化水稻的研究

水稻生长素输出载体OsPIN1a可能参与调控水稻根负向光性反应。为了进一步研究其他OsPIN基因与水稻根负向光性的关系,以GenBank数据库报道的OsPIN1b核苷酸序列为基础,设计特异引物以RTPCR从水稻cDNA中扩增得到OsPIN1b基因。测序结果表明获得完整的OsPIN1b基因ORF序列;生物信息学分析表明,OsPIN1b基因序列全长1 665 bp,与已报道的序列相吻合,其GC含量为64.08%,编码554个氨基酸。进一步构建了该基因的GFP融合表达载体pCAMBIA-1301-OsPIN1b∷GFP并转化水稻中花11,分子检测和GUS染色表明外源片段已经成功整合到水稻基因组,为研...

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Published in广东农业科学 Vol. 42; no. 24; pp. 146 - 150
Main Author 胥华伟 王海 莫亿伟
Format Journal Article
LanguageChinese
Published 河南科技大学农学院,河南洛阳,471003%绍兴文理学院生命科学学院,浙江绍兴,312000 2015
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Abstract 水稻生长素输出载体OsPIN1a可能参与调控水稻根负向光性反应。为了进一步研究其他OsPIN基因与水稻根负向光性的关系,以GenBank数据库报道的OsPIN1b核苷酸序列为基础,设计特异引物以RTPCR从水稻cDNA中扩增得到OsPIN1b基因。测序结果表明获得完整的OsPIN1b基因ORF序列;生物信息学分析表明,OsPIN1b基因序列全长1 665 bp,与已报道的序列相吻合,其GC含量为64.08%,编码554个氨基酸。进一步构建了该基因的GFP融合表达载体pCAMBIA-1301-OsPIN1b∷GFP并转化水稻中花11,分子检测和GUS染色表明外源片段已经成功整合到水稻基因组,为研究OsPIN1b在水稻根负向光性中的作用奠定基础。
AbstractList 水稻生长素输出载体OsPIN1a可能参与调控水稻根负向光性反应。为了进一步研究其他OsPIN基因与水稻根负向光性的关系,以GenBank数据库报道的OsPIN1b核苷酸序列为基础,设计特异引物以RTPCR从水稻cDNA中扩增得到OsPIN1b基因。测序结果表明获得完整的OsPIN1b基因ORF序列;生物信息学分析表明,OsPIN1b基因序列全长1 665 bp,与已报道的序列相吻合,其GC含量为64.08%,编码554个氨基酸。进一步构建了该基因的GFP融合表达载体pCAMBIA-1301-OsPIN1b∷GFP并转化水稻中花11,分子检测和GUS染色表明外源片段已经成功整合到水稻基因组,为研究OsPIN1b在水稻根负向光性中的作用奠定基础。
Q945.7; 水稻生长素输出载体OsPIN1a可能参与调控水稻根负向光性反应.为了进一步研究其他OsPIN基因与水稻根负向光性的关系,以GenBank数据库报道的OsPIN1b核苷酸序列为基础,设计特异引物以RT-PCR从水稻cDNA中扩增得到OsPIN1b基因.测序结果表明获得完整的OsPIN1b基因ORF序列;生物信息学分析表明,OsPIN1b基因序列全长1 665 bp,与已报道的序列相吻合,其GC含量为64.08%,编码554个氨基酸.进一步构建了该基因的GFP融合表达载体pCAMBIA-1301-OsPIN1b∷GFP并转化水稻中花11,分子检测和GUS染色表明外源片段已经成功整合到水稻基因组,为研究OsPIN1b在水稻根负向光性中的作用奠定基础.
Author 胥华伟 王海 莫亿伟
AuthorAffiliation 河南科技大学农学院,河南洛阳471003 绍兴文理学院生命科学学院,浙江绍兴312000
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Author_FL XU Hua-wei
MO Yi-wei
WANG Hai
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DocumentTitleAlternate Construction and transformation of GFP fusion expression vector of rice OsPIN1b gene
DocumentTitle_FL Construction and transformation of GFP fusion expression vector of rice OsPIN1b gene
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Keywords 负向光性
OsPIN1b
水稻
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rice(Oryza sativa); OsPIN1b; negative phototropism
XU Hua-wei;WANG Hai;MO Yi-wei( 1. College of Agriculture, Henan University of Science and Techen.ology, Luoyang 471003, China; 2. School of Life Sciences, Shaoxing University, Shaoxing 312000, China )
Earlier research results showed that rice auxin efflux protein OsPIN1 a probably participated in regulating negative phototropism of rice roots. To explore the relationship between other OsPIN genes and negative phototropism of rice roots,gene-specific primers were used to amplify Os PIN1 b gene by RT-PCR based on the OsPIN1 b sequence in Gen Bank. Sequencing result showed that the full ORF was obtained(1 665 bp). Bioinformation analysis showed that the sequence was 100% identity with the reported sequence,the GC content of OsPIN1 b ORF was 64.08% and OsPIN1 b encoded 554 amino acid residues. The OsPIN1b-green fluorescent protein(gfp)fusion expression vector p CAMBIA-1301-Os PIN1b∷GFP was constructed and transformed into Japonicarice Zhonghua11 by Agrobac
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SubjectTerms OsPIN1b
水稻
负向光性
Title 水稻OsPIN1b基因GFP融合表达载体构建及转化水稻的研究
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