Sequence and structure of the coding region of the human H-ras-1 gene from T24 bladder carcinoma cells.

O Fasano, E Taparowsky, J Fiddes, M Wigler, M Goldfarb
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Abstract

We have molecularly cloned and sequenced cDNA to the transcript of H-ras-1, the transforming gene of the T24 human bladder carcinoma cell line. The transcript derives from at least five exons in the H-ras-1 gene, and RNA splicing occurs at sites typical of exon-intron junctions. T24 H-ras-1 RNA has an AUG-initiated open reading frame of 567 nucleotides, which can encode a protein of mass comparable to the apparent molecular weight of the T24 H-ras-1 gene product. The T24 H-ras-1 gene product is nearly identical to v-H-ras p21, the transforming protein encoded by the genome of Harvey sarcoma virus. We discuss the implications of this sequence conservation in the structure-function relationships of ras proteins.

T24人膀胱癌细胞H-ras-1基因编码区的序列和结构。
我们对T24人膀胱癌细胞系转化基因H-ras-1的转录物进行了分子克隆和cDNA测序。转录本来自H-ras-1基因的至少五个外显子,RNA剪接发生在典型的外显子-内含子连接位点。T24 H-ras-1 RNA具有一个由aug启动的567个核苷酸的开放阅读框,可以编码一个质量与T24 H-ras-1基因产物表观分子量相当的蛋白质。T24 H-ras-1基因产物与哈维肉瘤病毒基因组编码的转化蛋白v-H-ras p21几乎相同。我们讨论了这种序列保守在ras蛋白结构-功能关系中的意义。
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