Shapira R, Choi G H, Nuss D L
Department of Molecular Oncology and Virology, Roche Institute of Molecular Biology, Roche Research Center, Nutley, NJ 07110.
EMBO J. 1991 Apr;10(4):731-9. doi: 10.1002/j.1460-2075.1991.tb08004.x.
The complete nucleotide sequence of the largest double-stranded (ds) RNA present in hypovirulent strain EP713 of the chestnut blight pathogen, Cryphonectria parasitica, was determined and the predicted genetic organization was confirmed by translational mapping analysis. The deduced RNA sequence was 12 712 bp in length, excluding the terminal poly(A):poly(U) homopolymer domain. The strand terminating with 3'-poly(A) contained two contiguous large open reading frames (ORF A and ORF B) beginning at nucleotide residues 496-498 and extending to nucleotide positions 11 859-11 861. The junction between ORF A and ORF B consisted of the sequence 5'-UAAUG-3', where UAA served as the termination codon for ORF A and AUG was the 5'-proximal initiation codon within ORF B. ORF A (622 codons in length, excluding the termination codon) was recently shown to encode two polypeptides, p29 and p40, which were generated from a nascent polyprotein by an autocatalytic event mediated by p29 (Choi et al., 1991). A similar autocatalytic event was observed during in vitro translation of ORF B (3165 codons in length) resulting in the release of a 48 kd polypeptide from the amino-terminal portion of the ORF B-encoded polyprotein. These results are discussed in terms of the opportunities they provide for elucidating the molecular basis of transmissible hypovirulence and possible origins of hypovirulence-associated dsRNAs.
测定了栗疫病菌低毒力菌株EP713中存在的最大双链(ds)RNA的完整核苷酸序列,并通过翻译图谱分析证实了预测的基因组织。推导的RNA序列长度为12712 bp,不包括末端的聚(A):聚(U)同聚物结构域。以3'-聚(A)结尾的链包含两个连续的大开放阅读框(ORF A和ORF B),起始于核苷酸残基496 - 498,延伸至核苷酸位置11859 - 11861。ORF A和ORF B之间的连接处由序列5'-UAAUG-3'组成,其中UAA作为ORF A的终止密码子,AUG是ORF B内5'-近端起始密码子。最近发现ORF A(长度为622个密码子,不包括终止密码子)编码两种多肽,p29和p40,它们是由新生多蛋白通过p29介导的自催化事件产生的(Choi等人,1991)。在ORF B(长度为3165个密码子)的体外翻译过程中观察到类似的自催化事件,导致从ORF B编码的多蛋白的氨基末端部分释放出一种48 kd的多肽。根据它们为阐明可传播低毒力的分子基础和低毒力相关dsRNA的可能起源提供的机会来讨论这些结果。