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CCAAT 框对人胸苷激酶 mRNA 表达的作用。

CCAAT-box contributions to human thymidine kinase mRNA expression.

作者信息

Mao X, Xia L, Liang G, Gai X, Huang D Y, Prystowsky M B, Lipson K E

机构信息

Jefferson Cancer Institute, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.

出版信息

J Cell Biochem. 1995 Apr;57(4):701-10. doi: 10.1002/jcb.240570415.

Abstract

In order to examine the role of two inverted CCAAT boxes near the start of transcription of the human thymidine kinase (TK) gene, a series of constructs were prepared in which one or both CCAAT boxes were deleted or mutated. These altered promoters (1.2 kb of 5'-flanking sequence) were used to express a TK minigene containing the first two exons and introns followed by the remainder of the cDNA. RNA blots were prepared from stable cell lines of ts13 cells containing these constructs under three conditions: 1) serum deprived cells, 2) serum stimulated cells, and 3) cells that had been stimulated with serum, but were arrested in the G1 phase of the cell cycle by the temperature sensitive mutation carried by these cells. TK mRNA expression from each construct was suppressed by the temperature sensitive block to cell cycle progression. Measurement of protein expression from the various altered TK promoters indicated that both CCAAT boxes contribute to promoter strength. These experiments also suggested that the two CCAAT boxes were not equivalent and that the distal CCAAT could substitute for the proximal CCAAT, but the converse was not true.

摘要

为了研究人胸苷激酶(TK)基因转录起始位点附近两个反向CCAAT框的作用,制备了一系列构建体,其中一个或两个CCAAT框被删除或突变。这些改变的启动子(5'侧翼序列的1.2 kb)用于表达一个TK小基因,该小基因包含前两个外显子和内含子,随后是cDNA的其余部分。在三种条件下,从含有这些构建体的ts13细胞稳定细胞系中制备RNA印迹:1)血清剥夺细胞,2)血清刺激细胞,3)用血清刺激但因这些细胞携带的温度敏感突变而停滞在细胞周期G1期的细胞。每种构建体的TK mRNA表达都被对细胞周期进程的温度敏感阻滞所抑制。对各种改变的TK启动子的蛋白质表达测量表明,两个CCAAT框都对启动子强度有贡献。这些实验还表明,两个CCAAT框并不等同,远端CCAAT可以替代近端CCAAT,但反之则不然。

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