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克隆的感染性新西兰黑鼠嗜异性小鼠白血病病毒的包膜和长末端重复序列

Envelope and long terminal repeat sequences of a cloned infectious NZB xenotropic murine leukemia virus.

作者信息

O'Neill R R, Buckler C E, Theodore T S, Martin M A, Repaske R

出版信息

J Virol. 1985 Jan;53(1):100-6. doi: 10.1128/JVI.53.1.100-106.1985.

Abstract

An infectious NZB xenotropic murine leukemia virus (MuLV) provirus (NZB was molecularly cloned from the Hirt supernatant of NZB-IU-6-infected mink cells, and the nucleotide sequence of its env gene and long terminal repeat (LTR) was determined. The partial nucleotide sequence previously reported for the env gene of NFS-Th-1 xenotropic proviral DNA (Repaske, et al., J. Virol. 46:204-211, 1983) is identical to that of the infectious NZB xenotropic MuLV DNA reported here. Alignment of nucleotide or deduced amino acid sequences, or both, of xenotropic, mink cell focus-forming, and ecotropic MuLV proviral DNAs in the env region identified sequence differences among the three host range classes of C-type MuLVs. Major differences were confined to the 5' half of env; a high degree of homology was found among the three classes of MuLVs in the 3' half of env. Alignment of the nucleotide sequence of the LTR of NZB xenotropic MuLV with those of the LTRs of NFS-Th-1 xenotropic, mink cell focus-forming, and ecotropic MuLVs revealed extensive homology between the LTRs of xenotropic and MCF247 MuLVs. An inserted 6-base-pair repeat 5' to the TATA box was a unique feature of both NZB and NFS-Th-1 xenotropic LTRs.

摘要

一种具有感染性的新西兰黑鼠嗜异性鼠白血病病毒(MuLV)前病毒(NZB是从感染了NZB - IU - 6的水貂细胞的Hirt上清液中进行分子克隆得到的,并测定了其env基因和长末端重复序列(LTR)的核苷酸序列。先前报道的NFS - Th - 1嗜异性前病毒DNA的env基因部分核苷酸序列(Repaske等人,《病毒学杂志》46:204 - 211,1983)与本文报道的具有感染性的新西兰黑鼠嗜异性MuLV DNA的序列相同。对嗜异性、水貂细胞集落形成和嗜亲性MuLV前病毒DNA在env区域的核苷酸或推导氨基酸序列(或两者)进行比对,确定了C型MuLVs的三种宿主范围类别之间的序列差异。主要差异局限于env的5'端一半;在env的3'端一半,三类MuLVs之间发现了高度同源性。将新西兰黑鼠嗜异性MuLV的LTR核苷酸序列与NFS - Th - 1嗜异性、水貂细胞集落形成和嗜亲性MuLV的LTR核苷酸序列进行比对,发现嗜异性和MCF247 MuLV的LTR之间存在广泛同源性。在TATA框5'端插入的一个6碱基对重复序列是新西兰黑鼠和NFS - Th - 1嗜异性LTR的独特特征。

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