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离散的空间和时间顺式作用元件调控拟南芥花同源异型基因APETALA3的转录。

Discrete spatial and temporal cis-acting elements regulate transcription of the Arabidopsis floral homeotic gene APETALA3.

作者信息

Hill T A, Day C D, Zondlo S C, Thackeray A G, Irish V F

机构信息

Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT 06520, USA.

出版信息

Development. 1998 May;125(9):1711-21. doi: 10.1242/dev.125.9.1711.

DOI:10.1242/dev.125.9.1711
PMID:9521909
Abstract

The APETALA3 floral homeotic gene is required for petal and stamen development in Arabidopsis. APETALA3 transcripts are first detected in a meristematic region that will give rise to the petal and stamen primordia, and expression is maintained in this region during subsequent development of these organs. To dissect how the APETALA3 gene is expressed in this spatially and temporally restricted domain, various APETALA3 promoter fragments were fused to the uidA reporter gene encoding beta-glucuronidase and assayed for the resulting patterns of expression in transgenic Arabidopsis plants. Based on these promoter analyses, we defined cis-acting elements required for distinct phases of APETALA3 expression, as well as for petal-specific and stamen-specific expression. By crossing the petal-specific construct into different mutant backgrounds, we have shown that several floral genes, including APETALA3, PISTILLATA, UNUSUAL FLORAL ORGANS, and APETALA1, encode trans-acting factors required for second-whorl-specific APETALA3 expression. We have also shown that the products of the APETALA1, APETALA3, PISTILLATA and AGAMOUS genes bind to several conserved sequence motifs within the APETALA3 promoter. We present a model whereby spatially and temporally restricted APETALA3 transcription is controlled via interactions between proteins binding to different domains of the APETALA3 promoter.

摘要

APETALA3花同源异型基因是拟南芥花瓣和雄蕊发育所必需的。APETALA3转录本首先在一个将产生花瓣和雄蕊原基的分生组织区域中被检测到,并且在这些器官随后的发育过程中,该区域持续表达。为了剖析APETALA3基因在这个时空受限的区域中是如何表达的,将各种APETALA3启动子片段与编码β-葡萄糖醛酸酶的uidA报告基因融合,并检测转基因拟南芥植株中产生的表达模式。基于这些启动子分析,我们定义了APETALA3表达不同阶段以及花瓣特异性和雄蕊特异性表达所需的顺式作用元件。通过将花瓣特异性构建体导入不同的突变背景,我们已经表明,包括APETALA3、PISTILLATA、异常花器官和APETALA1在内的几个花基因,编码第二轮特异性APETALA3表达所需的反式作用因子。我们还表明,APETALA1、APETALA3、PISTILLATA和AGAMOUS基因的产物与APETALA3启动子内的几个保守序列基序结合。我们提出了一个模型,通过结合到APETALA3启动子不同结构域的蛋白质之间的相互作用,来控制APETALA3在空间和时间上受限的转录。

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