Hannig E M, Thiele D J, Leibowitz M J
Mol Cell Biol. 1984 Jan;4(1):101-9. doi: 10.1128/mcb.4.1.101-109.1984.
The M double-stranded RNA component of type 1 killer strains of the yeast Saccharomyces cerevisiae contains an internal 200-base pair adenine- and uracil-rich region. The plus strands of this viral genomic RNA contain an internal adenine-rich region which allows these strands to bind to polyuridylate-Sepharose as tightly as do polyadenylated RNAs with 3'-terminal polyadenylated tracts of 70 to 100 residues. Internal template coding of an adenine-rich tract in positive polarity in vivo and in vitro transcripts of M double-stranded RNA may serve as an alternate method of transcript polyadenylation. The 3'-terminal residue of the in vitro m transcript is a non-template-encoded purine residue. The 5' terminus of this transcript is involved in a stem-and-loop structure which includes an AUG initiation codon, along with potential 18S and 5.8S rRNA binding sites. Except for the 3'-terminal residue, transcription in in vitro shows complete fidelity.
酿酒酵母1型杀伤菌株的M双链RNA组分含有一个内部200个碱基对的富含腺嘌呤和尿嘧啶的区域。这种病毒基因组RNA的正链含有一个内部富含腺嘌呤的区域,这使得这些链与聚尿苷酸-琼脂糖的结合程度与具有70至100个残基的3'-末端聚腺苷酸化序列的聚腺苷酸化RNA一样紧密。M双链RNA在体内和体外转录本中以正极性对富含腺嘌呤序列进行内部模板编码,这可能是转录本聚腺苷酸化的另一种方法。体外m转录本的3'-末端残基是一个非模板编码的嘌呤残基。该转录本的5'末端参与一个茎环结构,该结构包括一个AUG起始密码子以及潜在的18S和5.8S rRNA结合位点。除了3'-末端残基外,体外转录显示出完全的保真度。