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在GB肝炎病原体中鉴定出两个黄病毒样基因组。

Identification of two flavivirus-like genomes in the GB hepatitis agent.

作者信息

Simons J N, Pilot-Matias T J, Leary T P, Dawson G J, Desai S M, Schlauder G G, Muerhoff A S, Erker J C, Buijk S L, Chalmers M L

机构信息

Virus Discovery Group, Abbott Laboratories, North Chicago, IL 60064, USA.

出版信息

Proc Natl Acad Sci U S A. 1995 Apr 11;92(8):3401-5. doi: 10.1073/pnas.92.8.3401.

Abstract

A subtractive PCR methodology known as representational difference analysis was used to clone specific nucleotide sequences present in the infectious plasma from a tamarin infected with the GB hepatitis agent. Eleven unique clones were identified, seven of which were examined extensively. All seven clones appeared to be derived from sequences exogenous to the genomes of humans, tamarins, Saccharomyces cerevisiae, and Escherichia coli. In addition, sequences from these clones were not detected in plasma or liver tissue of tamarins prior to their inoculation with the GB agent. These sequences were detected by reverse transcription-PCR in acute-phase plasma of tamarins inoculated with the GB agent. Probes derived from two of the seven clones detected an RNA species of > or = 8.3 kb in the liver of a GB-agent-infected tamarin by Northern blot hybridization. Sequence analysis indicated that five of the seven clones encode polypeptides that possess limited amino acid identity with the nonstructural proteins of hepatitis C virus. Extension of the sequences found in the seven clones revealed that plasma from an infected tamarin contained two RNA molecules > 9 kb long. Limited sequence identity with various isolates of hepatitis C virus and the relative positions of putative RNA helicases and RNA-dependent RNA polymerases in the predicted protein products of these molecules suggested that the GB agent contains two unique flavivirus-like genomes.

摘要

一种称为代表性差异分析的消减PCR方法被用于克隆感染GB肝炎病原体的绢毛猴感染性血浆中存在的特定核苷酸序列。鉴定出11个独特的克隆,其中7个被广泛研究。所有7个克隆似乎都源自人类、绢毛猴、酿酒酵母和大肠杆菌基因组之外的序列。此外,在绢毛猴接种GB病原体之前,在其血浆或肝脏组织中未检测到这些克隆的序列。通过逆转录PCR在接种GB病原体的绢毛猴急性期血浆中检测到这些序列。从7个克隆中的2个克隆获得的探针通过Northern印迹杂交在感染GB病原体的绢毛猴肝脏中检测到一种大小≥8.3 kb的RNA物种。序列分析表明,7个克隆中的5个克隆编码的多肽与丙型肝炎病毒的非结构蛋白具有有限的氨基酸同源性。对7个克隆中发现的序列进行延伸分析发现,感染绢毛猴的血浆中含有两个长度大于9 kb的RNA分子。这些分子预测的蛋白质产物与丙型肝炎病毒的各种分离株具有有限的序列同源性,以及假定的RNA解旋酶和RNA依赖性RNA聚合酶的相对位置,表明GB病原体含有两个独特的黄病毒样基因组。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ce/42174/ddad56c07f19/pnas01492-0335-a.jpg

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