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AtGRP5 调控区的组织表达模式受正、负调控元件的共同控制。

The tissue expression pattern of the AtGRP5 regulatory region is controlled by a combination of positive and negative elements.

机构信息

Laboratório de Genômica Funcional e Transdução de Sinal, Departamento de Genética, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.

出版信息

Plant Cell Rep. 2010 May;29(5):461-71. doi: 10.1007/s00299-010-0835-7. Epub 2010 Feb 27.

Abstract

The AtGRP5 gene from Arabidopsis thaliana encodes a glycine-rich protein which has a major activity in protoderm-derived cells and is expressed in cells that undergo the first anatomical modifications leading to somatic embryo development. It has been previously demonstrated that its minimum promoter is 316 bp long including the 5'UTR and presents three putative TATA-boxes sequences and several regions that are homologous to previous characterized cis-acting elements. In order to better characterize the AtGRP5 expression and to identify the promoter regions involved in its preferential epidermal expression, in situ hybridization and 5' promoter deletions were employed. In situ hybridization and GUS expression assays indicate that, besides being present during somatic embryogenesis, AtGRP5 is also expressed during the zygotic embryo development. The sequential 5' deletions indicate that multiple negative and positive regulatory elements are present in the AtGRP5 promoter and operate in order to confer its distinct expression pattern. A 44-bp region was shown to be essential for the epidermal expression of this gene in leaves, stems, flowers and fruits, and is also responsible for high activity of the AtGRP5 promoter in zygotic embryos. An element responsible for the phloem expression was also identified in a 35-bp region.

摘要

来自拟南芥的 AtGRP5 基因编码一个甘氨酸丰富的蛋白,该蛋白在原表皮细胞中具有主要活性,并在经历导致体细胞胚胎发育的第一个解剖学修饰的细胞中表达。先前已经证明,其最小启动子长 316bp,包括 5'UTR,并具有三个假定的 TATA 框序列和几个与先前表征的顺式作用元件同源的区域。为了更好地表征 AtGRP5 的表达并鉴定参与其表皮表达的启动子区域,采用了原位杂交和 5'启动子缺失。原位杂交和 GUS 表达分析表明,除了在体细胞胚胎发生期间存在外,AtGRP5 在合子胚发育过程中也表达。连续的 5'缺失表明,AtGRP5 启动子中存在多个负调控和正调控元件,它们协同作用以赋予其独特的表达模式。一个 44-bp 的区域对于该基因在叶片、茎、花和果实中的表皮表达是必需的,并且还负责 AtGRP5 启动子在合子胚中的高活性。在一个 35-bp 的区域中也鉴定到一个负责韧皮部表达的元件。

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