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天冬酰胺合成酶人cDNA的分离及其在詹森大鼠肉瘤细胞中的表达。

Isolation of human cDNAs for asparagine synthetase and expression in Jensen rat sarcoma cells.

作者信息

Andrulis I L, Chen J, Ray P N

出版信息

Mol Cell Biol. 1987 Jul;7(7):2435-43. doi: 10.1128/mcb.7.7.2435-2443.1987.

Abstract

Asparagine synthetase cDNAs containing the complete coding region were isolated from a human fibroblast cDNA library. DNA sequence analysis of the clones showed that the message contained one open reading frame encoding a protein of 64,400 Mr, 184 nucleotides of 5' untranslated region, and 120 nucleotides of 3' noncoding sequence. Plasmids containing the asparagine synthetase cDNAs were used in DNA-mediated transfer of genes into asparagine-requiring Jensen rat sarcoma cells. The cDNAs containing the entire protein-coding sequence expressed asparagine synthetase activity and were capable of conferring asparagine prototrophy on the Jensen rat sarcoma cells. However, cDNAs which lacked sequence for as few as 20 amino acids at the amino terminal could not rescue the cells from auxotrophy. The transferant cell lines contained multiple copies of the human asparagine synthetase cDNAs and produced human asparagine synthetase mRNA and asparagine synthetase protein. Several transferants with numerous copies of the cDNAs exhibited only basal levels of enzyme activity. Treatment of these transferant cell lines with 5-azacytidine greatly increased the expression of asparagine synthetase mRNA, protein, and activity.

摘要

从人成纤维细胞cDNA文库中分离出包含完整编码区的天冬酰胺合成酶cDNA。对这些克隆进行DNA序列分析表明,该信使RNA包含一个编码64400 Mr蛋白质的开放阅读框、184个核苷酸的5'非翻译区和120个核苷酸的3'非编码序列。含有天冬酰胺合成酶cDNA的质粒用于将基因通过DNA介导转移到需要天冬酰胺的詹森大鼠肉瘤细胞中。包含完整蛋白质编码序列的cDNA表达天冬酰胺合成酶活性,并能够使詹森大鼠肉瘤细胞获得天冬酰胺原养型。然而,在氨基末端缺少多达20个氨基酸序列的cDNA无法使细胞从营养缺陷型中挽救出来。转移细胞系包含多个拷贝的人天冬酰胺合成酶cDNA,并产生人天冬酰胺合成酶mRNA和天冬酰胺合成酶蛋白。几个含有大量cDNA拷贝的转移细胞系仅表现出基础水平的酶活性。用5-氮杂胞苷处理这些转移细胞系可大大增加天冬酰胺合成酶mRNA、蛋白质和活性的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bf4/365375/e4eefe3b8b3c/molcellb00079-0147-a.jpg

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