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跨膜生长素载体系统——生长素极性运输的动态调节因子

Transmembrane auxin carrier systems--dynamic regulators of polar auxin transport.

作者信息

Morris D A

机构信息

Cell Sciences Division, School of Biological Sciences, University of Southampton, Southampton, UK.

出版信息

Plant Growth Regul. 2000 Nov;32(2-3):161-72. doi: 10.1023/a:1010701527848.

Abstract

Recent investigations of the biochemistry, physiology and molecular genetics of polar auxin transport have greatly advanced our understanding of the process and of the part it plays in the regulation of development and in the responses of cells, tissues and organs to internal and external stimuli. The molecular and physiological characterization of mutants which exhibit lesions in polar auxin transport has led to the isolation and sequencing of genes which encode putative components of auxin carrier systems, or proteins which directly or indirectly regulate these systems. This work has revealed that specific auxin uptake and efflux carriers are coded not by single genes, but by whole families of genes, the expression of which is tissue or stimulus specific. Furthermore, evidence is accumulating rapidly that at least the auxin efflux carrier is a multi-component system consisting of both catalytic and regulatory subunits, including a separate phytotropin-binding protein. Other genes have been tentatively identified which code proteins that regulate the expression of genes coding auxin carrier components, or which regulate the intracellular traffic or activity of auxin carriers. Investigations of the turn-over and Golgi-mediated trafficking of auxin carrier proteins have revealed that essential components of at least the efflux carrier have a very short half-life in the plasma membrane and are replaced without the need for concurrent protein synthesis, leading to speculation that they might cycle between internal stores and the plasma membrane. The way is now clear for the development of specific molecular probes with which to investigate the intracellular transport and targeting of auxin carrier proteins.

摘要

最近对极性生长素运输的生物化学、生理学和分子遗传学的研究极大地推进了我们对这一过程的理解,以及它在发育调控中所起的作用,和细胞、组织及器官对内部和外部刺激的反应中所起的作用。对在极性生长素运输中表现出损伤的突变体进行分子和生理学特征分析,已导致分离和测序编码生长素载体系统假定组分的基因,或直接或间接调节这些系统的蛋白质的基因。这项工作表明,特定的生长素摄取和外排载体不是由单个基因编码,而是由整个基因家族编码,其表达具有组织特异性或刺激特异性。此外,越来越多的证据表明至少生长素外排载体是一个多组分系统,由催化亚基和调节亚基组成,包括一种单独的植物生长素结合蛋白。其他基因已被初步鉴定出来,它们编码调节生长素载体组分编码基因表达的蛋白质,或调节生长素载体的细胞内运输或活性的蛋白质。对生长素载体蛋白的周转和高尔基体介导的运输的研究表明,至少外排载体的基本组分在质膜中的半衰期非常短,并且在不需要同时进行蛋白质合成的情况下被替换,这引发了一种推测,即它们可能在内部储存库和质膜之间循环。现在开发用于研究生长素载体蛋白细胞内运输和靶向的特异性分子探针的道路已经畅通。

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