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首页> 外文期刊>Journal of Experimental Botany >Analysis of CFB, a cytokinin-responsive gene of Arabidopsis thaliana encoding a novel F-box protein regulating sterol biosynthesis
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Analysis of CFB, a cytokinin-responsive gene of Arabidopsis thaliana encoding a novel F-box protein regulating sterol biosynthesis

机译:CFB分析,拟南芥Cytokinin响应基因编码新型F箱蛋白调节甾醇生物合成

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摘要

Protein degradation by the ubiquitin-26S proteasome pathway is important for the regulation of cellular processes, but the function of most F-box proteins relevant to substrate recognition is unknown. We describe the analysis of the gene Cytokinin-induced F-box encoding (CFB, AT3G44326), identified in a meta-analysis of cytokinin-related transcriptome studies as one of the most robust cytokinin response genes. F-box domain-dependent interaction with the E3 ubiquitin ligase complex component ASK1 classifies CFB as a functional F-box protein. Apart from F-box and transmembrane domains, CFB contains no known functional domains. CFB is expressed in all plant tissues, predominantly in root tissue. A ProCFB: GFP-GUS fusion gene showed strongest expression in the lateral root cap and during lateral root formation. CFB-GFP fusion proteins were mainly localized in the nucleus and the cytosol but also at the plasma membrane. cfb mutants had no discernible phenotype, but CFB overexpressing plants showed several defects, such as a white upper inflorescence stem, similar to the hypomorphic cycloartenol synthase mutant cas1-1. Both CFB overexpressing plants and cas1-1 mutants accumulated the CAS1 substrate 2,3-oxidosqualene in the white stem tissue, the latter even more after cytokinin treatment, indicating impairment of CAS1 function. This suggests that CFB may link cytokinin and the sterol biosynthesis pathway.
机译:蛋白质蛋白质蛋白酶体途径的蛋白质降解对于细胞过程的调节是重要的,但与底物识别相关的大多数F箱蛋白的功能是未知的。我们描述了在Cytokinin相关转录组研究的Meta分析中鉴定为最强大的细胞素响应基因之一的Meta分析中的基因细胞素诱导的F型盒编码(CFB,AT3G44326)的分析。与E3泛素连接酶复合组分ASK1将CFB分类为功能性F箱蛋白的F盒依赖性相互作用。除F盒和跨膜结构域外,CFB还没有已知的功能域。 CFB在所有植物组织中表达,主要是根组织。 ProCFB:GFP-GUS融合基因在侧根帽和侧根形成期间显示出最强的表达。 CFB-GFP融合蛋白主要是核和胞嘧啶的本地化,但也在质膜上。 CFB突变体没有可辨别的表型,但CFB过表达植物表现出几种缺陷,例如白色上部花序茎,类似于脱甲环戊烯醇合酶突变体Cas1-1。 CFB过表达植物和CAS1-1突变体累积在白色茎组织中的Cas1基板2,3-氧代喹啉,后者在细胞蛋白处理后更多,表明CAS1功能的损伤。这表明CFB可以将细胞蛋白和甾醇生物合成途径链接。

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