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敲除一个假定的转运蛋白会导致衣藻中蓝光信号传导发生改变。

Knock-out of a putative transporter results in altered blue-light signalling in Chlamydomonas.

作者信息

Dame Gregory, Gloeckner Gernot, Beck Christoph F

机构信息

Institut für Biologie III, Universität Freiburg, Schaenzlestrasse 1, D-79104 Freiburg, Germany.

出版信息

Plant J. 2002 Sep;31(5):577-87. doi: 10.1046/j.1365-313x.2002.01379.x.

Abstract

Nitrogen starvation and blue light are the two environmental cues that control sexual differentiation in Chlamydomonas reinhardtii. Insertional mutagenesis was applied to generate mutants that still require nitrogen starvation as the initiating signal for gametogenesis but were no longer dependent on irradiation. In one mutant analysed, sequences adjacent to the site of insertion were cloned and used for the isolation of a genomic clone that, upon transformation, could complement the mutant phenotype. The gene identified (LRG6) encodes two mRNAs that appear to be the products of differential splicing. The two putative gene products derived from these mRNAs differ in their C-terminal ends. Both predicted gene products exhibit multiple hydrophobic domains with alpha-helical secondary structure typical for integral membrane proteins. These proteins may form pores, and may function as transporters of as-yet unknown substrates. Since rendering the LRG6 gene non-functional resulted in light-independence of gamete formation, it is suggested that this transporter may inhibit signal flux from the photoreceptor to target genes - either directly by its activity or indirectly by serving as a scaffold for signalling proteins. Shutting off this transporter may be required for the activation of signal flux in this pathway. This concept is supported by the observed reduction in LRG6 mRNA levels during the first phase of gametic differentiation.

摘要

氮饥饿和蓝光是控制莱茵衣藻性别分化的两个环境信号。采用插入诱变来产生突变体,这些突变体在配子发生时仍需要氮饥饿作为起始信号,但不再依赖光照。在分析的一个突变体中,克隆了与插入位点相邻的序列,并用于分离一个基因组克隆,该克隆在转化后能够互补突变体表型。鉴定出的基因(LRG6)编码两种mRNA,它们似乎是可变剪接的产物。源自这些mRNA的两种假定基因产物在其C末端有所不同。两种预测的基因产物都具有多个疏水结构域,具有典型的整合膜蛋白的α-螺旋二级结构。这些蛋白质可能形成孔道,并可能作为尚未知底物的转运蛋白发挥作用。由于使LRG6基因失去功能导致配子形成不依赖光照,因此表明这种转运蛋白可能直接通过其活性或间接通过作为信号蛋白的支架来抑制从光感受器到靶基因的信号通量。关闭这种转运蛋白可能是激活该途径中信号通量所必需的。这一概念得到了在配子分化第一阶段观察到的LRG6 mRNA水平降低的支持。

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