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一个棉花 RING 型泛素连接酶(E3)基因的特性与启动子分析。

Characterization and promoter analysis of a cotton RING-type ubiquitin ligase (E3) gene.

机构信息

Department of Biochemistry and Molecular Biology, Mississippi State University, Mississippi State, Box 9650, MS, 39762, USA.

出版信息

Mol Biotechnol. 2010 Oct;46(2):140-8. doi: 10.1007/s12033-010-9280-7.

Abstract

A cotton fiber cDNA, GhRING1, and its corresponding gene have been cloned and characterized. The GhRING1 gene encodes a RING-type ubiquitin ligase (E3) containing 338 amino acids (aa). The GhRING1 protein contains a RING finger motif with conserved cysteine and histine residues at the C-terminus, and is classified as a C(3)H(2)C(3)-type RING protein. Blast searches show that GhRING1 has the highest homology to At3g19950, a zinc finger family protein from Arabidopsis. Real time RT-PCR analysis indicates that the GhRING1 gene is expressed in cotton fibers in a developmental manner. The transcript level of GhRING1 gene reaches a maximum in elongating fibers at 15 days post-anthesis (DPA). In vitro auto-ubiquitination assays using wheat germ extract and a reconstitution system demonstrate that GhRING1 has the ubiquitin E3 ligase activity. The histochemical GUS assay was performed to analyze tissue specificity of the GhRING1 and At3g19950 promoters in transgenic Arabidopsis plants. The GUS assay shows that the promoter of At3g19950 is highly activated in leaves, roots, trichomes, and also in anthers and stigma of flowers. In contrast, the GUS expression directed by the GhRING1 promoter is only located at stipules and anthers. The expression pattern of GhRING1 suggests that protein ubiquitination and turnover may be involved in transition to different stages of cotton fiber development.

摘要

一个棉花纤维 cDNA,GhRING1,及其对应的基因已经被克隆和鉴定。GhRING1 基因编码一个 RING 型泛素连接酶(E3),包含 338 个氨基酸(aa)。GhRING1 蛋白含有一个 RING 指基序,在 C 末端保守的半胱氨酸和组氨酸残基,被分类为 C(3)H(2)C(3)-型 RING 蛋白。Blast 搜索表明 GhRING1 与拟南芥的 At3g19950 具有最高的同源性,At3g19950 是一个锌指家族蛋白。实时 RT-PCR 分析表明,GhRING1 基因在棉花纤维中以发育方式表达。GhRING1 基因的转录水平在开花后 15 天(DPA)伸长纤维中达到最大值。使用小麦胚提取物和重建系统进行的体外自动泛素化测定表明,GhRING1 具有泛素 E3 连接酶活性。组织化学 GUS 测定用于分析 GhRING1 和 At3g19950 启动子在转基因拟南芥植物中的组织特异性。GUS 测定表明,At3g19950 启动子在叶片、根、毛状体中高度激活,也在花的花药和柱头中激活。相比之下,由 GhRING1 启动子指导的 GUS 表达仅位于托叶和花药中。GhRING1 的表达模式表明,蛋白质泛素化和周转可能参与棉花纤维发育的不同阶段的转变。

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