van Wezenbeek P, Verver J, Harmsen J, Vos P, van Kammen A
EMBO J. 1983;2(6):941-6. doi: 10.1002/j.1460-2075.1983.tb01525.x.
Middle component RNA (M RNA) of cowpea mosaic virus (CPMV) was transcribed into cDNA and double-stranded cDNA was inserted into the EcoRI site of plasmid pBRH2. The nucleotide sequence of inserts was determined, after subcloning in bacteriophages M13mp7, M13mp8 or M13mp9, by the dideoxy chain termination method. The complete sequence of CPMV M RNA, up to the poly(A) tail, is 3481 nucleotides long. The sequence contains a long open reading frame starting at nucleotide 161 from the 5' terminus and continuing to 180 nucleotides from the 3' terminus. The sequence does not contain a polyadenylation signal for the poly(A) tail at the 3' end of CPMV RNA. The initiation site at position 161 together with AUG codons in the same reading frame at positions 512 and/or 524 account for the two large colinear precursor polypeptides translated in vitro from M RNA. The amino acid sequence deduced from the nucleotide sequence suggests that both precursor polypeptides are proteolytically cleaved at glutaminyl-methionine and glutaminyl-glycine, respectively, to produce the two viral capsid proteins.
豇豆花叶病毒(CPMV)的中间组分RNA(M RNA)被转录成cDNA,双链cDNA被插入质粒pBRH2的EcoRI位点。在亚克隆到噬菌体M13mp7、M13mp8或M13mp9中后,通过双脱氧链终止法测定插入片段的核苷酸序列。CPMV M RNA直至聚腺苷酸尾的完整序列长度为3481个核苷酸。该序列包含一个长的开放阅读框,从5'末端的第161个核苷酸开始,一直延续到3'末端的第180个核苷酸。该序列在CPMV RNA的3'末端不包含用于聚腺苷酸尾的聚腺苷酸化信号。161位的起始位点与512位和/或524位同一阅读框中的AUG密码子共同构成了从M RNA体外翻译的两种大的共线性前体多肽。从核苷酸序列推导的氨基酸序列表明,两种前体多肽分别在谷氨酰胺基 - 甲硫氨酸和谷氨酰胺基 - 甘氨酸处被蛋白水解切割,以产生两种病毒衣壳蛋白。