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为在酵母细胞核中表达而设计的线粒体基因的化学合成。

Chemical synthesis of a mitochondrial gene designed for expression in the yeast nucleus.

作者信息

Gearing D P, McMullen G L, Nagley P

出版信息

Biochem Int. 1985 Jun;10(6):907-15.

PMID:2931082
Abstract

A novel DNA sequence coding for subunit 8 of the mitochondrial ATPase of Saccharomyces cerevisiae has been constructed by chemical synthesis. The synthetic gene, termed NAP1, is designed for expression in the yeast nucleus and codes for a 48 amino acid polypeptide identical to that encoded by the mitochondrial aap1 gene of S. cerevisiae. The codons chosen for the NAP1 sequence correspond almost exclusively to those most frequently occurring in highly expressed yeast genes. The NAP1 coding region differs in 31 codons from that of aap1, and is flanked by sequences carrying restriction enzyme sites useful for cloning and for gene expression. A 170 bp double stranded DNA molecule was constructed by assembling 12 oligonucleotides (12 to 45 bases in length) in a single annealing/ligation mixture. This synthetic gene will provide a route for the systematic manipulation, through in vitro mutagenesis, of the structure of a protein normally encoded by mitochondrial DNA.

摘要

通过化学合成构建了一种编码酿酒酵母线粒体ATP酶8亚基的新DNA序列。这个合成基因被称为NAP1,设计用于在酵母细胞核中表达,编码一种48个氨基酸的多肽,与酿酒酵母线粒体aap1基因编码的多肽相同。为NAP1序列选择的密码子几乎完全对应于高表达酵母基因中最常出现的密码子。NAP1编码区与aap1的编码区在31个密码子上不同,两侧是带有用于克隆和基因表达的限制酶位点的序列。通过在单一退火/连接混合物中组装12个寡核苷酸(长度为12至45个碱基)构建了一个170 bp的双链DNA分子。这个合成基因将为通过体外诱变对通常由线粒体DNA编码的蛋白质结构进行系统操作提供一条途径。

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