Sumner-Smith M, Hottinger H, Willis I, Koch T L, Arentzen R, Söll D
Mol Gen Genet. 1984;197(3):447-52. doi: 10.1007/BF00329941.
We have cloned and sequenced the wild-type and suppressor alleles of the S. pombe sup8 tRNA gene. The wild-type allele has a leucine UAA anticodon and the suppressor (sup8-e) carries the opal suppressor anticodon UCA. The gene has a 16 base pair intervening sequence that, in the RNA, is predicted to form a secondary structure which involves base pairing to the 5', rather than the usual 3' side of the 5' splice site. When incubated in Saccharomyces cerevisiae cell-free extracts both alleles are efficiently transcribed, the 5' leader and 3' trailer sequences are removed and CCA is added to the 3' processed end; however, the intervening sequence is not excised. This finding implies that the structural requirements of the splicing endonucleases in the two yeasts have diverged. No other tRNA genes with related sequences were detected in S. pombe DNA by hybridization, suggesting that other UUA isoacceptors may be structurally dissimilar to sup8 or that the UUA codon may be decoded by a UUG leucine isoacceptor.
我们已经克隆并测序了粟酒裂殖酵母sup8 tRNA基因的野生型和抑制子等位基因。野生型等位基因具有亮氨酸UAA反密码子,而抑制子(sup8-e)携带乳白抑制子反密码子UCA。该基因有一个16个碱基对的间隔序列,在RNA中,预计会形成一种二级结构,该结构涉及与5'剪接位点的5'端而非通常的3'端进行碱基配对。当在酿酒酵母无细胞提取物中孵育时,两个等位基因都能高效转录,5'前导序列和3'尾随序列被去除,并且CCA被添加到3'加工末端;然而,间隔序列并未被切除。这一发现意味着两种酵母中剪接内切核酸酶的结构要求已经发生了分化。通过杂交在粟酒裂殖酵母DNA中未检测到其他具有相关序列的tRNA基因,这表明其他UUA同功受体在结构上可能与sup8不同,或者UUA密码子可能由UUG亮氨酸同功受体解码。