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白色念珠菌翻译延伸因子3编码基因的分离与序列分析。

Isolation and sequence analysis of the gene encoding translation elongation factor 3 from Candida albicans.

作者信息

Di Domenico B J, Lupisella J, Sandbaken M, Chakraburtty K

机构信息

Schering-Plough Research Institute, Bloomfield, NJ 07003.

出版信息

Yeast. 1992 May;8(5):337-52. doi: 10.1002/yea.320080502.

Abstract

The structural gene encoding translation elongation factor 3 (EF-3) has been cloned from a Candida albicans genomic library by hybridization to a Saccharomyces cerevisiae probe containing the Saccharomyces gene, YEF3 (Sandbaken et al., 1990b). The sequences were shown to be functionally homologous to the Saccharomyces gene by three criteria: (1) a Saccharomyces strain transformed with a high copy plasmid containing CaEF3 sequences overproduces the EF-3 peptide two-fold; (2) extracts from this strain exhibit a two-fold increase in the EF-3-catalysed, ribosome-dependent ATPase activity (Kamath and Chakraburtty, 1988); and (3) the Candida gene complements a Saccharomyces null mutant. The coding region, identified by DNA sequencing, indicates that CaEF3 encodes a 1050 amino acid polypeptide having a potential molecular weight of 116,865 Da. This protein shows 77% overall identity to the Saccharomyces YEF3 gene, with a significantly greater identity (94%) concentrated in the region of the protein thought to contain the catalytic domain of EF-3 (Sandbaken et al., 1990a). The upstream non-coding region contains T-rich regions typical of many yeast genes and several potential RAP1/GRF1 elements shown to regulate expression of a number of translational genes (Mager, 1988). The data confirm a high degree of conservation for EF-3 among the two organisms.

摘要

通过与含有酿酒酵母基因YEF3的酿酒酵母探针杂交,从白色念珠菌基因组文库中克隆出了编码翻译延伸因子3(EF-3)的结构基因(Sandbaken等人,1990b)。通过三个标准表明这些序列与酿酒酵母基因在功能上具有同源性:(1)用含有CaEF3序列的高拷贝质粒转化的酿酒酵母菌株,其EF-3肽的产量增加了两倍;(2)该菌株的提取物中,EF-3催化的、依赖核糖体的ATP酶活性增加了两倍(Kamath和Chakraburtty,1988);(3)白色念珠菌基因可互补酿酒酵母的缺失突变体。通过DNA测序确定的编码区表明,CaEF3编码一种1050个氨基酸的多肽,其潜在分子量为116,865道尔顿。该蛋白与酿酒酵母YEF3基因的总体一致性为77%,在被认为包含EF-3催化结构域的蛋白区域,一致性显著更高(94%)(Sandbaken等人,1990a)。上游非编码区含有许多酵母基因典型的富含T的区域以及几个潜在的RAP1/GRF1元件,这些元件已被证明可调节许多翻译基因的表达(Mager,1988)。这些数据证实了两种生物中EF-3的高度保守性。

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