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猴B淋巴细胞嗜性乳头多瘤病毒DNA:复制起点周围区域的核苷酸序列

Monkey B-lymphotropic papovavirus DNA: nucleotide sequence of the region around the origin of replication.

作者信息

Furuno A, Miyamura T, Yoshiike K

出版信息

J Virol. 1984 May;50(2):451-6. doi: 10.1128/JVI.50.2.451-456.1984.

Abstract

We have determined the nucleotide sequence of the HindIII-B DNA segment of African green monkey B-lymphotropic papovavirus (LPV), which shows a highly restricted host range and whose genome is a 5.1-kilobase-long circular DNA. The segment, consisting of 1,123 base pairs, contained the origin of DNA replication, the putative control region for early transcription, and the region probably coding for the amino-terminal portion of T antigens. The symmetrical region at the center of replication origin, 5'-GAGGC CA GGGGCCCC TA GCCTC-3' (on the L strand), has diverged in the central portion from the corresponding regions of primate polyomaviruses simian virus 40, BK virus, and JC virus, but resembles that of mouse polyomavirus. The structure of the control region upstream of the replication origin was unique to LPV and contained several repeated sequences, the longest of which were two 60-base-pair tandem repeats. The amino-terminal region common to LPV small T and large T antigens showed some homology (41%) in the deduced amino acid sequence to that of both simian virus 40 and the mouse polyomavirus. Like other polyomaviruses, the probable carboxyl-terminal region unique to LPV small T antigen contained two sets of the Cys-x-Cys-x-x-Cys structure. These data show that, despite the unique structures in the control region, LPV is evolutionally related to the mouse polyomavirus and to simian virus 40.

摘要

我们已经确定了非洲绿猴B淋巴细胞嗜性乳头瘤病毒(LPV)的HindIII - B DNA片段的核苷酸序列,该病毒显示出高度受限的宿主范围,其基因组是一个5.1千碱基长的环状DNA。该片段由1123个碱基对组成,包含DNA复制起点、早期转录的假定控制区以及可能编码T抗原氨基末端部分的区域。复制起点中心的对称区域,5'-GAGGC CA GGGGCCCC TA GCCTC-3'(在L链上),在中心部分与灵长类多瘤病毒猴病毒40、BK病毒和JC病毒的相应区域有所不同,但与小鼠多瘤病毒的相似。复制起点上游控制区的结构是LPV特有的,包含几个重复序列,其中最长的是两个60碱基对的串联重复序列。LPV小T抗原和大T抗原共有的氨基末端区域在推导的氨基酸序列中与猴病毒40和小鼠多瘤病毒的氨基末端区域有一些同源性(41%)。与其他多瘤病毒一样,LPV小T抗原特有的可能的羧基末端区域包含两组Cys-x-Cys-x-x-Cys结构。这些数据表明,尽管控制区有独特结构,但LPV在进化上与小鼠多瘤病毒和猴病毒40相关。

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