Bostian K A, Burn V E, Jayachandran S, Tipper D J
Nucleic Acids Res. 1983 Feb 25;11(4):1077-97. doi: 10.1093/nar/11.4.1077.
In vivo transcripts of the L (4.5 kb) and M (1.9 kb) dsRNA plasmids were examined in type I killers of Saccharomyces cerevisiae. Transcripts for both plasmids include full-length (l,m) and partial-length (la,ma) single-stranded species. Both L-dsRNA transcripts (l,la) have in vitro mRNA activity for L-P1, previously shown to be identical to ScV-P1, the 88,000 dalton major capsid protein of the virus-like particles containing L- and M1-dsRNAs. 1, but not 1a, is bound to poly(U)-sepharose and may be polyadenylated. Other L-dsRNA gene products and their transcripts may exist. For M1-dsRNA, both species (m, ma) have in vitro mRNA activity for M1-P1, the 32,000 dalton pre-protoxin encoded by M1-dsRNA. Both m and ma are bound to poly(U)-Sepharose and ma is probably a 5' terminal fragment of m. A functional model for M1-dsRNA killer plasmid structure is presented.
在酿酒酵母的I型杀伤细胞中检测了L(4.5 kb)和M(1.9 kb)双链RNA质粒的体内转录本。两种质粒的转录本都包括全长(l、m)和部分长度(la、ma)的单链种类。两种L-双链RNA转录本(l、la)对L-P1具有体外mRNA活性,L-P1先前已证明与ScV-P1相同,ScV-P1是含有L-和M1-双链RNA的病毒样颗粒的88,000道尔顿主要衣壳蛋白。1(而非1a)与聚(U)-琼脂糖结合,可能被聚腺苷酸化。可能存在其他L-双链RNA基因产物及其转录本。对于M1-双链RNA,两种种类(m、ma)对M1-P1具有体外mRNA活性,M1-P1是由M1-双链RNA编码的32,000道尔顿前原毒素。m和ma都与聚(U)-琼脂糖结合,ma可能是m的5'末端片段。提出了M1-双链RNA杀伤质粒结构的功能模型。