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用于在水稻中发现基因功能的模式化GAL4-VP16反式激活系统的建立。

Establishment of a patterned GAL4-VP16 transactivation system for discovering gene function in rice.

作者信息

Liang Dacheng, Wu Changyin, Li Caishun, Xu Caiguo, Zhang Jianwei, Kilian Andrzej, Li Xianghua, Zhang Qifa, Xiong Lizhong

机构信息

National Key Laboratory of Crop Genetic Improvement, National Center of Plant Gene Research (Wuhan), Huazhong Agricultural University, Wuhan 430070, China.

出版信息

Plant J. 2006 Jun;46(6):1059-72. doi: 10.1111/j.1365-313X.2006.02747.x.

Abstract

A binary GAL4-VP16-UAS transactivation system has been established in rice (Oryza sativa L.) in this study for the discovery of gene functions. This binary system consists of two types of transgenic lines, pattern lines and target lines. The pattern lines were produced by transformation of Zhonghua 11, a japonica cultivar, with a construct consisting of the transactivator gene GAL4-VP16 controlled by a minimal promoter and the GUSplus reporter controlled by the upstream activation sequence (UAS; cis-element to GAL4). Target lines were generated by transformation of Zhonghua 11 with constructs carrying the EGFP reporter and target genes of interest, both controlled by the UAS but in opposite directions. Hybrid plants were obtained by crossing target lines of 10 putative transcription factor genes from rice with six pattern lines showing expression in anther, stigma, palea, lemma and leaves. The EGFP and target genes perfectly co-expressed in hybrid plants with the same expression patterns as in the pattern lines. Various phenotypic changes, such as delayed flowering, multiple pistils, dwarfism, narrow and droopy leaves, reduced tillers, growth retardation and sterility, were induced as a result of the expression of the target genes. It is concluded that this transactivation system can provide a useful tool in rice to unveil latent functions of unknown or known genes.

摘要

本研究在水稻(Oryza sativa L.)中建立了一种二元GAL4-VP16-UAS反式激活系统,用于发现基因功能。该二元系统由两种转基因株系组成,即模式株系和靶标株系。模式株系是通过用一个构建体转化粳稻品种中花11而产生的,该构建体由一个由最小启动子控制的反式激活基因GAL4-VP16和一个由上游激活序列(UAS;GAL4的顺式元件)控制的GUSplus报告基因组成。靶标株系是通过用携带EGFP报告基因和感兴趣的靶标基因的构建体转化中花11而产生的,这两个基因均由UAS控制,但方向相反。通过将来自水稻的10个假定转录因子基因的靶标株系与6个在花药、柱头、内稃、外稃和叶片中表达的模式株系杂交,获得了杂交植株。EGFP和靶标基因在杂交植株中完美共表达,其表达模式与模式株系相同。由于靶标基因的表达,诱导了各种表型变化,如开花延迟、多雌蕊、矮化、叶片狭窄下垂、分蘖减少、生长迟缓以及不育。得出的结论是,这种反式激活系统可为水稻中揭示未知或已知基因的潜在功能提供一种有用的工具。

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