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编码人亚精胺/精胺N1-乙酰基转移酶的全长cDNA的特性分析。

Characterization of a full-length cDNA which codes for the human spermidine/spermine N1-acetyltransferase.

作者信息

Xiao L, Celano P, Mank A R, Pegg A E, Casero R A

机构信息

Oncology Center Laboratories, Johns Hopkins University School of Medicine, Baltimore, MD 21231.

出版信息

Biochem Biophys Res Commun. 1991 Aug 30;179(1):407-15. doi: 10.1016/0006-291x(91)91385-p.

DOI:10.1016/0006-291x(91)91385-p
PMID:1652956
Abstract

Spermidine/spermine N1-acetyltransferase is the rate-limiting enzyme in the catabolism of cellular polyamines. Using a combination of cDNA library screening and anchored PCR methodologies, a full length cDNA designated AP3/F7 corresponding to the human SSAT was cloned using RNA from the human large cell undifferentiated lung carcinoma line NCI H157. The resulting cDNA clone is 1,060 base pairs with a 513 base open reading frame coding for a 171 amino acid protein, with a predicted subunit molecular weight of 20,023. The 5' non-coding region of AP3/F7 is 165 bases and the 3' untranslated region is 382 bases with a polyadenylation site 20 bases 5' to the poly(A) tail. This full length cDNA should be an aid in the study of the regulation of spermidine/spermine N1-acetyltransferase expression and the significance of the acetyltransferase in polyamine metabolism.

摘要

亚精胺/精胺N1 - 乙酰基转移酶是细胞多胺分解代谢中的限速酶。通过结合cDNA文库筛选和锚定PCR方法,使用来自人类大细胞未分化肺癌细胞系NCI H157的RNA克隆了一个对应于人精胺/亚精胺N1 - 乙酰基转移酶(SSAT)的全长cDNA,命名为AP3/F7。得到的cDNA克隆为1060个碱基对,具有一个513个碱基的开放阅读框,编码一个171个氨基酸的蛋白质,预测亚基分子量为20,023。AP3/F7的5'非编码区为165个碱基,3'非翻译区为382个碱基,在多聚腺苷酸尾巴5'端20个碱基处有一个多聚腺苷酸化位点。这个全长cDNA应该有助于研究亚精胺/精胺N1 - 乙酰基转移酶表达的调控以及该乙酰基转移酶在多胺代谢中的意义。

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Characterization of a full-length cDNA which codes for the human spermidine/spermine N1-acetyltransferase.编码人亚精胺/精胺N1-乙酰基转移酶的全长cDNA的特性分析。
Biochem Biophys Res Commun. 1991 Aug 30;179(1):407-15. doi: 10.1016/0006-291x(91)91385-p.
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Isolation and characterization of a cDNA clone that codes for human spermidine/spermine N1-acetyltransferase.编码人精胺/亚精胺N1-乙酰基转移酶的cDNA克隆的分离与鉴定。
J Biol Chem. 1991 Jan 15;266(2):810-4.
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