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不同类型的乙型肝炎病毒(HBV)DNA整合体可能反映整合过程。

Different type of hepatitis B virus (HBV) DNA integrants that may reflect the integration process.

作者信息

Okubo K, Nakamura T, Tokino T, Matsubara K

机构信息

Institute for Molecular and Cellular Biology, Osaka University, Suita, Japan.

出版信息

Gastroenterol Jpn. 1990 Sep;25 Suppl 2:23-30. doi: 10.1007/BF02779924.

Abstract

Through analyses of HBV DNA integratns in human cellular DNA, we identified three different integrant types, each of which may reflect the process of primary integrant formation by the viral DNA. The first type, which we call "simple type" consists of integrants found in some hepatocellular carcinomas (HCC's). The structure of the viral genome is simple, and part of it is deleted. The viral cohesive end sequence appears at one of the viral-cellular DNA junctions, and integration has elicited a microdeletion in the target cellular DNA sequence. This structure suggests viral DNA replication intermediates as substrates for integration. Judging from its frequency in HCC, this type may represent the most preferred one, if not all, among the primary integration products. The second type, which we call "complex type" is essentially the same as the first type, except tht the viral genome structure is complex. We considered the possibility that they may have been produced via the same process, using preformed complex viral genomes such as "novel form DNA's" (Rogler and Summers, 1982) as substrates. In cultured fetal hepatocytes, integration of HBV DNA can occur only a few days after infection. Among such integrants, we found a third type integrant, having a simple viral genome, but having a larger cellular DNA deletion. We propose that different forms of viral DNA may be used as substrates in the integration process, and the process is characterized by its eliciting of deletions of different size in the target cellular DNA. The most preferred substrate may be the one producing the simple type integrants, and the most frequently occurring deletion in the target DNA may be the microdeletion.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过对人类细胞DNA中HBV DNA整合情况的分析,我们鉴定出三种不同的整合体类型,每种类型可能反映了病毒DNA形成初级整合体的过程。第一种类型,我们称之为“简单型”,存在于一些肝细胞癌(HCC)中。病毒基因组结构简单,部分发生了缺失。病毒粘性末端序列出现在病毒 - 细胞DNA连接处之一,并且整合引发了靶细胞DNA序列中的微缺失。这种结构表明病毒DNA复制中间体是整合的底物。从其在HCC中的频率判断,这种类型可能代表了初级整合产物中最优选的一种,如果不是全部的话。第二种类型,我们称之为“复杂型”,与第一种类型基本相同,只是病毒基因组结构复杂。我们考虑了它们可能通过相同过程产生的可能性,使用预先形成的复杂病毒基因组,如“新形式DNA”(Rogler和Summers,1982)作为底物。在培养的胎儿肝细胞中,HBV DNA整合仅在感染后几天发生。在这些整合体中,我们发现了第三种类型的整合体,其病毒基因组简单,但细胞DNA缺失更大。我们提出不同形式的病毒DNA可能在整合过程中用作底物,并且该过程的特征在于其在靶细胞DNA中引发不同大小的缺失。最优选的底物可能是产生简单型整合体的底物,并且靶DNA中最常出现的缺失可能是微缺失。(摘要截短于250字)

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