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本文引用的文献

1
Indole-3-acetamide-dependent auxin biosynthesis: a widely distributed way of indole-3-acetic acid production?吲哚-3-乙酰胺依赖的生长素生物合成:一种广泛分布的吲哚-3-乙酸产生方式?
Eur J Cell Biol. 2010 Dec;89(12):895-905. doi: 10.1016/j.ejcb.2010.06.021. Epub 2010 Aug 10.
2
Global analysis of gene activity during Arabidopsis seed development and identification of seed-specific transcription factors.拟南芥种子发育过程中基因活性的全局分析及种子特异性转录因子的鉴定。
Proc Natl Acad Sci U S A. 2010 May 4;107(18):8063-70. doi: 10.1073/pnas.1003530107. Epub 2010 Apr 12.
3
Auxin biosynthesis and its role in plant development.生长素的生物合成及其在植物发育中的作用。
Annu Rev Plant Biol. 2010;61:49-64. doi: 10.1146/annurev-arplant-042809-112308.
4
Biochemical analyses of indole-3-acetaldoxime-dependent auxin biosynthesis in Arabidopsis.拟南芥中吲哚 - 3 - 乙醛肟依赖性生长素生物合成的生化分析。
Proc Natl Acad Sci U S A. 2009 Mar 31;106(13):5430-5. doi: 10.1073/pnas.0811226106. Epub 2009 Mar 11.
5
The NtAMI1 gene functions in cell division of tobacco BY-2 cells in the presence of indole-3-acetamide.在吲哚-3-乙酰胺存在的情况下,NtAMI1基因在烟草BY-2细胞的细胞分裂中发挥作用。
FEBS Lett. 2009 Jan 22;583(2):487-92. doi: 10.1016/j.febslet.2008.12.049. Epub 2008 Dec 31.
6
LEAFY COTYLEDON1 is a key regulator of fatty acid biosynthesis in Arabidopsis.叶状子叶1是拟南芥中脂肪酸生物合成的关键调节因子。
Plant Physiol. 2008 Oct;148(2):1042-54. doi: 10.1104/pp.108.126342. Epub 2008 Aug 8.
7
Identification and characterization of carrot HAP factors that form a complex with the embryo-specific transcription factor C-LEC1.与胚胎特异性转录因子C-LEC1形成复合物的胡萝卜HAP因子的鉴定与特性分析
J Exp Bot. 2007;58(13):3819-28. doi: 10.1093/jxb/erm238.
8
A Homoeotic Mutant of Arabidopsis thaliana with Leafy Cotyledons.拟南芥的同源突变体,具有叶状子叶。
Science. 1992 Dec 4;258(5088):1647-50. doi: 10.1126/science.258.5088.1647.
9
Arabidopsis amidase 1, a member of the amidase signature family.拟南芥酰胺酶1,酰胺酶特征家族的一员。
FEBS J. 2007 Jul;274(13):3440-51. doi: 10.1111/j.1742-4658.2007.05876.x. Epub 2007 Jun 6.
10
CONSTANS and the CCAAT box binding complex share a functionally important domain and interact to regulate flowering of Arabidopsis.CONSTANS与CCAAT盒结合复合体共享一个功能重要的结构域,并相互作用以调控拟南芥的开花。
Plant Cell. 2006 Nov;18(11):2971-84. doi: 10.1105/tpc.106.043299. Epub 2006 Nov 30.

在发芽后的前两天,AMIDASE1(AMI1)的表达受到抑制。

Expression of AMIDASE1 (AMI1) is suppressed during the first two days after germination.

机构信息

Centro de Biotecnología y Genómica de Plantas (U.P.M. - I.N.I.A.), Campus de Montegancedo, Pozuelo de Alarcón (Madrid), Spain.

出版信息

Plant Signal Behav. 2010 Dec;5(12):1642-4. doi: 10.4161/psb.5.12.13810. Epub 2010 Dec 1.

DOI:10.4161/psb.5.12.13810
PMID:21150258
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3115122/
Abstract

The regulation of cellular auxin levels is a critical factor in determining plant growth and architecture, as indole-3-acetic acid (IAA) gradients along the plant axis and local IAA maxima are known to initiate numerous plant growth responses. The regulation of auxin homeostasis is mediated in part by transport, conjugation and deconjugation, as well as by de novo biosynthesis. However, the pathways of IAA biosynthesis are yet not entirely characterized at the molecular and biochemical level. It is suggested that several biosynthetic routes for the formation of IAA have evolved. One such pathway proceeds via the intermediate indole-3-acetamide (IAM), which is converted into IAA by the activity of specific IAM hydrolases, such as Arabidopsis AMIDASE1 (AMI1). In this article we present evidence to support the argument that AMI1-dependent IAA synthesis is likely not to be used during the first two days of seedling development.

摘要

细胞内生长素水平的调节是决定植物生长和形态建成的关键因素,因为已知植物轴上的吲哚-3-乙酸 (IAA) 梯度和局部 IAA 最大值会引发许多植物生长反应。生长素的动态平衡主要通过运输、共轭和去共轭以及从头生物合成来调节。然而,在分子和生化水平上,IAA 生物合成的途径尚未完全阐明。有人提出,已经形成了几种 IAA 形成的生物合成途径。其中一条途径是通过中间产物吲哚-3-乙酰胺 (IAM) 进行的,IAM 可以通过特定的 IAM 水解酶(如拟南芥酰胺酶 1(AMI1))的活性转化为 IAA。在本文中,我们提供了证据支持这样一个观点,即 AMI1 依赖性 IAA 合成在幼苗发育的头两天可能不会被利用。