Bally M, Hughes J, Cesareni G
European Molecular Biology Laboratory, Heidelberg, FRG.
Nucleic Acids Res. 1988 Jun 24;16(12):5291-303. doi: 10.1093/nar/16.12.5291.
The gene for a previously unidentified small nuclear RNA has been cloned from Saccharomyces cerevisiae and its nucleotide sequence has been determined. The RNA, snR30, was mapped to a unique coding sequence 605 nucleotides long. SnR30 appears to be one of the most abundant snRNAs of S, cerevisiae in that it can be resolved by ethidium bromide staining on one-dimensional denaturing gels of total yeast RNA. Like other snRNAs, snR30 is enriched in nuclei preparations and possesses a trimethyl guanosine cap structure at its 5' end. After substituting one allele of the wild type gene in a diploid strain for a deleted gene, after sporulation, haploid strains carrying the deletion were unable to grow, indicating that snR30 is required for an essential, but as yet, unknown function. The nucleotide sequence close to the initiation site of the SNR30 gene is similar to that of other yeast SNR genes whose transcripts are associated with pre-rRNA, suggesting that snR30 is related to this group of snRNAs.
一个之前未被鉴定的小核RNA基因已从酿酒酵母中克隆出来,其核苷酸序列也已确定。该RNA,即snR30,被定位到一个长度为605个核苷酸的独特编码序列上。SnR30似乎是酿酒酵母中最丰富的snRNA之一,因为在总酵母RNA的一维变性凝胶上,它可以通过溴化乙锭染色分辨出来。与其他snRNA一样,snR30在细胞核提取物中富集,并且在其5'端具有一个三甲基鸟苷帽结构。在二倍体菌株中将野生型基因的一个等位基因替换为缺失基因后,经过孢子形成,携带该缺失的单倍体菌株无法生长,这表明snR30对于一种必需但尚未明确的功能是必需的。靠近SNR30基因起始位点的核苷酸序列与其他酵母SNR基因的序列相似,这些基因的转录本与前体rRNA相关,这表明snR30与这组snRNA有关。