Hodge M R, Cumsky M G
Department of Molecular Biology and Biochemistry, University of California, Irvine 92717.
Mol Cell Biol. 1989 Jun;9(6):2765-70. doi: 10.1128/mcb.9.6.2765-2770.1989.
The Saccharomyces cerevisiae COX5b gene contains a small intron that is unique in two respects. First, it interrupts the ATG codon that initiates translation of the COX5b product. Second, it contains a sequence at the 5' splice junction (5'-GCATGT-3') that differs from the highly conserved yeast hexanucleotide (5'-GTAPyGT-3') and from the 5'-GT found at the corresponding position in nearly all introns of eucaryotic protein-coding genes. We have analyzed both the transcripts derived from the COX5b gene and the splicing of its intron. We show here that an unspliced mRNA precursor constituted a minor fraction of the total COX5b message, even when the gene was overexpressed. We also show that both major transcripts derived from COX5b had been spliced. Our results suggest that at least in the case of COX5b, a 5'-GC can function as efficiently as the highly conserved 5'-GT in the splicing reaction.
酿酒酵母COX5b基因含有一个小内含子,该内含子在两个方面具有独特性。首先,它打断了启动COX5b产物翻译的ATG密码子。其次,它在5'剪接位点(5'-GCATGT-3')含有一个序列,该序列不同于高度保守的酵母六核苷酸(5'-GTAPyGT-3')以及几乎所有真核生物蛋白质编码基因内含子相应位置处的5'-GT。我们分析了源自COX5b基因的转录本及其内含子的剪接情况。我们在此表明,即使该基因过表达,未剪接的mRNA前体在COX5b总信息中也只占一小部分。我们还表明,源自COX5b的两个主要转录本都已被剪接。我们的结果表明,至少就COX5b而言,5'-GC在剪接反应中能像高度保守的5'-GT一样有效地发挥作用。