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玉米a1基因启动子中的转座子插入对Myb因子P和C1的转录有不同影响。

Transposon insertions in the promoter of the Zea mays a1 gene differentially affect transcription by the Myb factors P and C1.

作者信息

Pooma Wilailak, Gersos Christos, Grotewold Erich

机构信息

Department of Plant Biology and Plant Biotechnology Center, The Ohio State University, Columbus, Ohio 43210, USA.

出版信息

Genetics. 2002 Jun;161(2):793-801. doi: 10.1093/genetics/161.2.793.

Abstract

The understanding of control of gene regulation in higher eukaryotes relies heavily on results derived from non-in vivo studies, but rarely can the significance of these approximations be established in vivo. Here, we investigated the effect of Mutator and Spm insertions on the expression of the flavonoid biosynthetic gene a1, independently regulated by the transcription factors C1 and P. The a1-mum2 and a1-m2 alleles carry Mu1 and Spm insertions, respectively, in a cis-element (ARE) of unknown function located between the P- and C1-binding sites. We show that the insertions of Mu1 and Spm similarly influence the expression of a1 controlled by C1 or P. The P-controlled a1 expression in a1-m2 is Spm dependent, and the mutant phenotype of a1-mum2 is suppressed in the pericarp in the absence of the autonomous MuDR element. Footprints within the ARE affect the regulation of a1 by C1 and P differently, providing evidence that these factors control a1 expression using distinct cis-acting regulatory elements. Together, our findings contribute significantly to one of the best-described plant regulatory systems, while stressing the need to complement with in vivo experiments current approaches used for the study of control of gene expression.

摘要

对高等真核生物基因调控的理解在很大程度上依赖于非体内研究的结果,但这些近似结果在体内的意义却很少能得到证实。在此,我们研究了Mutator和Spm插入对类黄酮生物合成基因a1表达的影响,该基因由转录因子C1和P独立调控。a1-mum2和a1-m2等位基因分别在位于P结合位点和C1结合位点之间的一个功能未知的顺式元件(ARE)中携带Mu1和Spm插入。我们表明,Mu1和Spm的插入同样影响由C1或P控制的a1的表达。a1-m2中由P控制的a1表达依赖于Spm,并且在没有自主MuDR元件的情况下,a1-mum2的突变表型在果皮中受到抑制。ARE内的足迹对C1和P调控a1的方式有不同影响,这表明这些因子利用不同的顺式作用调控元件来控制a1的表达。总之,我们的发现对描述最详尽的植物调控系统之一有重大贡献,同时强调需要通过体内实验来补充当前用于研究基因表达调控的方法。

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