Herzog E, Guilley H, Manohar S K, Dollet M, Richards K, Fritsch C, Jonard G
Institut de Biologie Moléculaire des Plantes du CNRS et de l'Université Louis Pasteur, Strasbourg, France.
J Gen Virol. 1994 Nov;75 ( Pt 11):3147-55. doi: 10.1099/0022-1317-75-11-3147.
The complete nucleotide sequence of RNA 1 of the tentative furovirus peanut clump virus (PCV) has been determined by characterization of cloned cDNA and by direct RNA sequencing. The sequence is 5897 nucleotides in length and contains three long open reading frames (ORFs). The 5'-terminal proximal ORF has the potential to encode a polypeptide of M(r) 130942 (P131) containing methyltransferase and RNA helicase homologous domains and displaying homology with large nonstructural proteins of alpha-like viruses, which are known or thought to be involved in virus replication. The P131 ORF is followed in-frame by a second ORF which is probably expressed by partial readthrough of the UGA termination codon of the P131 ORF to produce a polypeptide of M(r) 191044 (P191). The readthrough region of P191 contains the characteristic 'core' RNA polymerase motif, indicating that the PCV replicase proteins are expressed as a pair of overlapping proteins as in the tobamoviruses, tobraviruses and the furovirus soil-borne wheat mosaic virus (SBWMV). Sequence comparisons indicate that P131 and P191 are most closely related to the replicase proteins of SBWMV and the hordeivirus barley stripe mosaic virus (BSMV) but are only distantly related to the replicase of the furovirus beet necrotic yellow vein virus (BNYVV). The 3'-terminal proximal ORF can encode a putative polypeptide of M(r) 14556 (P15) which displays homology to small cysteine-rich proteins of hordeiviruses and SBWMV. We have corrected four errors in the sequence of PCV RNA 2 published previously by Manohar et al. (Virology 195, 33-41, 1993). One of these changes causes two small ORFs near the 3' terminus of RNA 2 to be fused together to create an ORF for a putative polypeptide of M(r) 16833 (P17) which displays extensive homology with the third protein of the triple gene block of BSMV RNA beta.
通过对克隆cDNA的特性分析和直接RNA测序,已确定暂定的帚状病毒花生丛簇病毒(PCV)RNA 1的完整核苷酸序列。该序列长度为5897个核苷酸,包含三个长开放阅读框(ORF)。5'末端近端的ORF有可能编码一个M(r)130942(P131)的多肽,该多肽含有甲基转移酶和RNA解旋酶同源结构域,并与α-样病毒的大型非结构蛋白具有同源性,已知或认为这些蛋白参与病毒复制。P131 ORF之后是第二个ORF,它可能通过P131 ORF的UGA终止密码子的部分通读而表达,产生一个M(r)191044(P191)的多肽。P191的通读区域包含特征性的“核心”RNA聚合酶基序,表明PCV复制酶蛋白如烟草花叶病毒、烟草脆裂病毒和帚状病毒土传小麦花叶病毒(SBWMV)一样,作为一对重叠蛋白表达。序列比较表明,P131和P191与SBWMV和大麦病毒大麦条纹花叶病毒(BSMV)的复制酶蛋白关系最为密切,但与帚状病毒甜菜坏死黄脉病毒(BNYVV)的复制酶关系较远。3'末端近端的ORF可编码一个推定的M(r)14556(P15)多肽,该多肽与大麦病毒和SBWMV的富含半胱氨酸的小蛋白具有同源性。我们已纠正了Manohar等人(《病毒学》195,33 - 41,1993)先前发表的PCV RNA 2序列中的四个错误。其中一个变化导致RNA 2 3'末端附近的两个小ORF融合在一起,形成一个推定的M(r)16833(P17)多肽的ORF,该多肽与BSMV RNAβ的三基因块的第三个蛋白具有广泛的同源性。