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菠菜PsaD和PsaF基因的启动子和前导序列在烟草子叶中引导相反的光反应:ATG密码子下游的PsaD序列是正向光反应所必需的。

Promoter and leader sequences of the spinach PsaD and PsaF genes direct an opposite light response in tobacco cotyledons: PsaD sequences downstream of the ATG codon are required for a positive light response.

作者信息

Flieger K, Wicke A, Herrmann R G, Oelmüller R

机构信息

Botanisches Institut der Ludwig-Maximilans-Universität, München, Germany.

出版信息

Plant J. 1994 Sep;6(3):359-68. doi: 10.1046/j.1365-313x.1994.06030359.x.

Abstract

Subunits II and III of the photosystem I reaction centre are encoded by the nuclear genes PsaD and PsaF, respectively. In spinach, the expression of both genes is highly synchronized with regard to time, space and in response to stimulators such as light. Nevertheless, promoter sequences as well as the design and location of regulatory elements are strikingly different. Promoter and leader of PsaF, when fused to the GUS reporter gene, direct a positive light response in the cotyledons of transgenic tobacco seedlings. In contrast, the equivalent PsaD regions confer a negative-light regulation to the GUS gene. If a 6-kb fragment that contains 1802 bp of the promoter, the transcription unit as well as additional 2.5 kb downstream of the PsaD gene is introduced into tobacco, the transcript level from the PsaD transgene is positively light-regulated in tobacco cotyledons. Thus, regulatory elements of the spinach PsaD and PsaF promoters are arranged in a very different way and essential cis-determinants for the positive light response of the PsaD gene can be located within the coding region and/or even further downstream.

摘要

光系统I反应中心的亚基II和III分别由核基因PsaD和PsaF编码。在菠菜中,这两个基因的表达在时间、空间上以及对光等刺激的响应方面高度同步。然而,启动子序列以及调控元件的设计和位置却显著不同。当PsaF的启动子和前导序列与GUS报告基因融合时,可在转基因烟草幼苗的子叶中引导正向光反应。相反,PsaD的等效区域对GUS基因赋予负向光调控。如果将一个包含1802 bp启动子、转录单元以及PsaD基因下游另外2.5 kb的6 kb片段导入烟草,PsaD转基因在烟草子叶中的转录水平受到正向光调控。因此,菠菜PsaD和PsaF启动子的调控元件排列方式非常不同,PsaD基因正向光反应的关键顺式决定因素可能位于编码区内和/或更远的下游。

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