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从全长cDNA推导的甘薯线粒体F1-ATP合酶δ亚基前体的一级结构

Primary structure of a precursor for the delta-subunit of sweet potato mitochondrial F1-ATPase deduced from full length cDNA.

作者信息

Kimura T, Takeda S, Asahi T, Nakamura K

机构信息

Laboratory of Biochemistry, School of Agriculture, Nagoya University, Japan.

出版信息

J Biol Chem. 1990 Apr 15;265(11):6079-85.

PMID:1690722
Abstract

A cDNA library constructed from poly(A)-rich RNA of the sweet potato tuberous root using a newly developed plasmid vector carrying tac-SP6 promoters was used to identify full length cDNAs for the nuclear-encoded delta-subunit of mitochondrial F1-ATPase by oligonucleotide-hybridization selection. Selected clones contained cDNA insert which carry the entire coding capacity for the pre-delta-subunit, since the RNA transcribed in vitro from SP6 promoter on the vector directed the synthesis of pre-delta-subunit polypeptide in a wheat germ in vitro translation assay. The nucleotide sequence of one of these cDNAs indicates that it can code for the pre-delta-subunit of 244 amino acids of which 199 amino acids encode the mature subunit. The amino acid sequence of the mature delta-subunit shows similarities of about 18-25% amino acid positional identity with the delta-subunits of bacterial F1-ATPases, about 26% with the delta-subunit of chloroplast CF1-ATPase, and about 32-37% with oligomycin sensitivity conferring proteins of animal and fungal mitochondria. The N-terminal presequence of the precursor composed of maximum of 45 amino acids does not show any obvious sequence homology with either the transit peptide of the nuclear-encoded pre-delta-subunit of chloroplast CF1 or the presequence of the nuclear-encoded pre-oligomycin sensitivity conferring proteins. At least two types of the delta-subunit cDNAs with very similar structures were identified from the library, and the presence of multiple copies of the delta-subunit gene in the hexaploid genome of the sweet potato is also suggested by genomic Southern blot hybridization.

摘要

利用携带tac-SP6启动子的新开发质粒载体,从甘薯块根富含多聚腺苷酸(poly(A))的RNA构建了一个cDNA文库,通过寡核苷酸杂交筛选来鉴定线粒体F1-ATP酶核编码δ亚基的全长cDNA。所选克隆包含携带前体δ亚基完整编码能力的cDNA插入片段,因为载体上SP6启动子体外转录的RNA在小麦胚体外翻译试验中指导了前体δ亚基多肽的合成。其中一个cDNA的核苷酸序列表明,它可以编码244个氨基酸的前体δ亚基,其中199个氨基酸编码成熟亚基。成熟δ亚基的氨基酸序列与细菌F1-ATP酶的δ亚基显示出约18 - 25%的氨基酸位置同一性,与叶绿体CF1-ATP酶的δ亚基约26%相同,与动物和真菌线粒体的寡霉素敏感性赋予蛋白约32 - 37%相同。由最多45个氨基酸组成的前体的N端前序列与叶绿体CF1核编码前体δ亚基的转运肽或核编码前体寡霉素敏感性赋予蛋白的前序列均未显示出任何明显的序列同源性。从文库中鉴定出至少两种结构非常相似的δ亚基cDNA,基因组Southern印迹杂交也表明甘薯六倍体基因组中存在多个δ亚基基因拷贝。

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