Xu W B, Roufa D J
Center for Basic Cancer Research and Division of Biology, Kansas State University, Manhattan 66506, USA.
Gene. 1996 Mar 9;169(2):257-62. doi: 10.1016/0378-1119(96)88652-5.
Starting with a cloned cDNA encoding human ribosomal protein S24 [Brown et al., Gene 91 (1990) 293-296], we PCR-amplified two introns from the human RPS24 locus. These then were used as unique nucleic-acid probes to isolate a 12-kb RPS24 gene fragment from a library of human genomic DNA. The nucleotide sequence of human RPS24 (4942 bp), its exon-intron organization and mRNA transcription start point were determined using standard procedures. RT-PCR analyses of S24 mRNAs from multiple human tissues and cell lines revealed two mRNA isoforms which differ from each other, as well as murine S24 mRNAs due to alternative exon splices near the 3' end of the gene.
我们从一个编码人核糖体蛋白S24的克隆cDNA(Brown等人,《基因》91卷,第293 - 296页,1990年)开始,通过聚合酶链反应(PCR)从人RPS24基因座扩增出两个内含子。然后将这些内含子用作独特的核酸探针,从人基因组DNA文库中分离出一个12千碱基对(kb)的RPS24基因片段。使用标准程序确定了人RPS24的核苷酸序列(4942碱基对)、其外显子 - 内含子结构以及mRNA转录起始点。对来自多种人类组织和细胞系的S24 mRNA进行逆转录 - 聚合酶链反应(RT - PCR)分析,发现了两种彼此不同的mRNA异构体,并且由于该基因3'端附近外显子的选择性剪接,它们也与小鼠S24 mRNA不同。