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编码磷脂酰丝氨酸合酶的酵母PSS基因的核苷酸序列及特性分析

Nucleotide sequence and characterization of the yeast PSS gene encoding phosphatidylserine synthase.

作者信息

Nikawa J, Tsukagoshi Y, Kodaki T, Yamashita S

出版信息

Eur J Biochem. 1987 Aug 17;167(1):7-12. doi: 10.1111/j.1432-1033.1987.tb13297.x.

Abstract
  1. A yeast chromosomal DNA which contains the structural gene for phosphatidylserine synthase (PSS) was isolated by genetic complementation from a wild-type yeast genomic library. The PSS gene was subcloned into a 1.1-kb fragment of the yeast DNA on the YEp13 vector. 2. The PSS gene on the multicopy plasmid caused the fourfold over-production of the enzyme and fully restored the phosphatidylserine content of the transformant. The phospholipid composition of the transformant was similar to that of the wild type. 3. Sequence analysis showed that this DNA fragment contains an open reading frame capable of encoding 276 amino acid residues with a calculated relative molecular mass of 30,804. Northern blot analysis of poly(A)-rich RNA of the wild-type yeast indicated that this DNA segment is transcribed into a single mRNA species. 4. The DNA sequence contained two putative transcriptional initiation signals, each followed by the ATG initiator codon. Deletion experiments indicated that the 5'-proximal ATG codon is essential for the synthesis of the functional phosphatidylserine synthase.
摘要
  1. 通过基因互补从野生型酵母基因组文库中分离出一种包含磷脂酰丝氨酸合酶(PSS)结构基因的酵母染色体DNA。PSS基因被亚克隆到YEp13载体上酵母DNA的一个1.1 kb片段中。2. 多拷贝质粒上的PSS基因导致该酶产量增加四倍,并完全恢复了转化体中磷脂酰丝氨酸的含量。转化体的磷脂组成与野生型相似。3. 序列分析表明,该DNA片段包含一个开放阅读框,能够编码276个氨基酸残基,计算相对分子质量为30,804。对野生型酵母富含多聚腺苷酸(poly(A))的RNA进行Northern印迹分析表明,该DNA片段转录成单一的mRNA种类。4. DNA序列包含两个假定的转录起始信号,每个信号后面跟着ATG起始密码子。缺失实验表明,5'-近端ATG密码子对于功能性磷脂酰丝氨酸合酶的合成至关重要。

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