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拟南芥ERECTA基因在茎尖分生组织和器官原基中表达。

The Arabidopsis ERECTA gene is expressed in the shoot apical meristem and organ primordia.

作者信息

Yokoyama R, Takahashi T, Kato A, Torii K U, Komeda Y

机构信息

Division of Biological Sciences, Graduate School of Science, Hokkaido University, Sapporo, Japan.

出版信息

Plant J. 1998 Aug;15(3):301-10. doi: 10.1046/j.1365-313x.1998.00203.x.

DOI:10.1046/j.1365-313x.1998.00203.x
PMID:9750343
Abstract

In Arabidopsis thaliana (L.) Heynh, the mutation in ERECTA is known to confer a compact inflorescence by a reduction in the lengths of internodes and pedicels. We analyzed the expression pattern of this gene during plant development. In situ hybridization and histochemical analysis using transgenic plants carrying chimeric gene fusions, with the ERECTA promoter fused to the beta-glucuronidase (GUS) gene, showed that ERECTA was predominantly expressed in the shoot apical meristems and organ primordia. ERECTA expression in the shoot apical meristem was weak early in plant development but increased with the transition from the vegetative to the reproductive growth phase. ERECTA was also strongly expressed in organ primordia and immature organs but weakly in mature organs. Thus, ERECTA was expressed in a cell-specific and developmentally regulated manner. In order to identify the regulatory mechanism responsible for the expression pattern of ERECTA, the cis-acting regions in the ERECTA promoter were defined by study of the expression of the chimeric genes that consist of the 5'- or internal deleted promoter and a GUS reporter gene in transgenic plants. The results showed that the essential cis-regulatory elements governing the spatially and temporally specific expression of ERECTA are located between positions -462 and -228 bp and between positions -228 and -153 bp with respect to the transcriptional initiation site.

摘要

在拟南芥中,已知ERECTA基因的突变会通过缩短节间和花梗的长度来形成紧凑的花序。我们分析了该基因在植物发育过程中的表达模式。使用携带嵌合基因融合体的转基因植物进行原位杂交和组织化学分析,该融合体是将ERECTA启动子与β-葡萄糖醛酸酶(GUS)基因融合,结果表明ERECTA主要在茎尖分生组织和器官原基中表达。在植物发育早期,ERECTA在茎尖分生组织中的表达较弱,但随着从营养生长阶段向生殖生长阶段的转变而增加。ERECTA在器官原基和未成熟器官中也强烈表达,但在成熟器官中表达较弱。因此,ERECTA以细胞特异性和发育调控的方式表达。为了确定负责ERECTA表达模式的调控机制,通过研究由5'-缺失或内部缺失的启动子与GUS报告基因组成的嵌合基因在转基因植物中的表达,确定了ERECTA启动子中的顺式作用区域。结果表明,控制ERECTA在空间和时间上特异性表达的必需顺式调控元件位于相对于转录起始位点的-462至-228 bp之间以及-228至-153 bp之间。

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