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一种由HIV-1逆转录酶介导的非同源重组模型,解释了赋予复制适应性优势的序列基序重复现象。

A Model of Non-Homologous Recombination Mediated by HIV-1 Reverse Transcriptase Explaining Sequence Motif Duplications That Confer a Replication Fitness Advantage.

作者信息

Panchapakesan Arun, Ranga Udaykumar

机构信息

HIV-AIDS Laboratory, Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur, Bengaluru 560064, India.

Molecular Biology Laboratory, Y R Gaitonde Centre for AIDS Research and Education (YRG CARE), Chennai 600031, India.

出版信息

Viruses. 2025 May 7;17(5):680. doi: 10.3390/v17050680.

Abstract

The Reverse Transcriptase of the Human Immunodeficiency Virus (HIV) is distinguished by its high rate of homologous recombination. A less-studied consequence of this phenomenon is the increased occurrence of non-homologous recombination, which results in length polymorphism. While most of these genome-wide variations are sporadic, some provide a replication advantage to variant strains, such as those in the Long Terminal Repeat (LTR) and p6-Gag regions. By analyzing sequences from these two regions in the HIV-1 databases, we categorize all types of non-homologous recombination into four groups based on the presence or absence of two molecular features. Additionally, drawing on established models of homologous recombination, we propose a model that describes the process of sequence duplication. This model can also be applied to explain non-homologous recombination in different types of HIV and other viruses.

摘要

人类免疫缺陷病毒(HIV)的逆转录酶以其高同源重组率而著称。这种现象一个较少被研究的后果是,非同源重组的发生率增加,这导致了长度多态性。虽然这些全基因组变异大多是零星发生的,但有些变异为变异株提供了复制优势,比如长末端重复序列(LTR)和p6 - Gag区域的变异株。通过分析HIV - 1数据库中这两个区域的序列,我们根据两种分子特征的有无,将所有类型的非同源重组分为四类。此外,借鉴已有的同源重组模型,我们提出了一个描述序列重复过程的模型。这个模型也可用于解释不同类型HIV及其他病毒中的非同源重组。

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