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本文引用的文献

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Auxin transport in membrane vesicles from Cucurbita pepo L.南瓜膜囊泡中的生长素运输
Planta. 1983 Apr;157(3):193-201. doi: 10.1007/BF00405182.
2
Local treatment with indole-3-acetic acid induces differential growth responses in Zea mays L. roots.吲哚-3-乙酸的局部处理诱导玉米根的差异生长反应。
Planta. 1991 Aug;185(1):58-64. doi: 10.1007/BF00194515.
3
Indole-3-acetic acid levels after phytochrome-mediated changes in the stem elongation rate of dark- and light-grown Pisum seedlings.光形态建成介导的暗生长和光生长豌豆苗茎伸长率变化后吲哚-3-乙酸水平。
Planta. 1992 Aug;188(1):85-92. doi: 10.1007/BF00198943.
4
The aux1 Mutation of Arabidopsis Confers Both Auxin and Ethylene Resistance.拟南芥 aux1 突变体同时具有抗生长素和抗乙烯的特性。
Plant Physiol. 1990 Nov;94(3):1462-6. doi: 10.1104/pp.94.3.1462.
5
Auxin Transport Inhibitors: III. Chemical Requirements of a Class of Auxin Transport Inhibitors.生长素运输抑制剂:III. 一类生长素运输抑制剂的化学需求。
Plant Physiol. 1977 Dec;60(6):826-9. doi: 10.1104/pp.60.6.826.
6
Requirement of the Auxin Polar Transport System in Early Stages of Arabidopsis Floral Bud Formation.生长素极性运输系统在拟南芥花芽形成早期的需求
Plant Cell. 1991 Jul;3(7):677-684. doi: 10.1105/tpc.3.7.677.
7
An Auxin-Responsive Promoter Is Differentially Induced by Auxin Gradients during Tropisms.生长素梯度在向性运动过程中差异诱导生长素响应启动子。
Plant Cell. 1991 Nov;3(11):1167-1175. doi: 10.1105/tpc.3.11.1167.
8
Evidence for a Single Naphthylphthalamic Acid Binding Site on the Zucchini Plasma Membrane.西葫芦质膜上单个萘基邻苯二甲酸结合位点的证据。
Plant Physiol. 1993 Oct;103(2):449-456. doi: 10.1104/pp.103.2.449.
9
The N-1-Naphthylphthalamic Acid-Binding Protein Is an Integral Membrane Protein.N-1-萘基邻苯二甲酸结合蛋白是一种整合膜蛋白。
Plant Physiol. 1996 Jun;111(2):427-432. doi: 10.1104/pp.111.2.427.
10
Red light-regulated growth. I. Changes in the abundance of indoleacetic acid and a 22-kilodalton auxin-binding protein in the maize mesocotyl.红光调控生长。I. 玉米中胚轴中吲哚乙酸和一种22千道尔顿生长素结合蛋白丰度的变化。
Plant Physiol. 1991;97(1):352-8. doi: 10.1104/pp.97.1.352.

BIG:一种拟南芥中生长素极性运输所需的类钙调素蛋白。

BIG: a calossin-like protein required for polar auxin transport in Arabidopsis.

作者信息

Gil P, Dewey E, Friml J, Zhao Y, Snowden K C, Putterill J, Palme K, Estelle M, Chory J

机构信息

Plant Biology Laboratory, Howard Hughes Medical Institute, The Salk Institute for Biological Studies, La Jolla, California 92037 USA.

出版信息

Genes Dev. 2001 Aug 1;15(15):1985-97. doi: 10.1101/gad.905201.

DOI:10.1101/gad.905201
PMID:11485992
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC312751/
Abstract

Polar auxin transport is crucial for the regulation of auxin action and required for some light-regulated responses during plant development. We have found that two mutants of Arabidopsis-doc1, which displays altered expression of light-regulated genes, and tir3, known for its reduced auxin transport-have similar defects and define mutations in a single gene that we have renamed BIG. BIG is very similar to the Drosophila gene Calossin/Pushover, a member of a gene family also present in Caenorhabditis elegans and human genomes. The protein encoded by BIG is extraordinary in size, 560 kD, and contains several putative Zn-finger domains. Expression-profiling experiments indicate that altered expression of multiple light-regulated genes in doc1 mutants can be suppressed by elevated levels of auxin caused by overexpression of an auxin biosynthetic gene, suggesting that normal auxin distribution is required to maintain low-level expression of these genes in the dark. Double mutants of tir3 with the auxin mutants pin1, pid, and axr1 display severe defects in auxin-dependent growth of the inflorescence. Chemical inhibitors of auxin transport change the intracellular localization of the auxin efflux carrier PIN1 in doc1/tir3 mutants, supporting the idea that BIG is required for normal auxin efflux.

摘要

极性生长素运输对于生长素作用的调节至关重要,并且在植物发育过程中某些光调节反应中是必需的。我们发现拟南芥的两个突变体——doc1(其显示出光调节基因表达改变)和tir3(因其生长素运输减少而闻名)具有相似的缺陷,并且在我们重新命名为BIG的单个基因中发现了突变。BIG与果蝇基因Calossin/Pushover非常相似,该基因家族的一个成员也存在于秀丽隐杆线虫和人类基因组中。由BIG编码的蛋白质在大小上非常特别,为560 kD,并且包含几个假定的锌指结构域。表达谱实验表明,通过生长素生物合成基因过表达导致的生长素水平升高,可以抑制doc1突变体中多个光调节基因的表达改变,这表明正常的生长素分布对于在黑暗中维持这些基因的低水平表达是必需的。tir3与生长素突变体pin1、pid和axr1的双突变体在花序的生长素依赖性生长中表现出严重缺陷。生长素运输的化学抑制剂改变了doc1/tir3突变体中生长素流出载体PIN1的细胞内定位,支持了BIG是正常生长素流出所必需的这一观点。