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从主要组织相容性复合体的Q10和D区域分离病毒样(VL30)元件。

Isolation of virus-like (VL30) elements from the Q10 and D regions of the major histocompatibility complex.

作者信息

Choi Y C, Meruelo D

机构信息

Department of Pathology, New York University Medical Center, New York 10016.

出版信息

Biochem Genet. 1991 Feb;29(1-2):91-101. doi: 10.1007/BF00578242.

Abstract

Previous studies from our laboratory have described two endogenous provirus-like sequences in a series of cosmids spanning the TL region of the major histocompatibility complex (MHC) of normal C57BL/10 mice. At least one of these viruses shares similarities with VL30 elements. To determine if additional VL30-like retroviral elements are integrated in the MHC, we constructed a cosmid library using DNA from a radiation leukemia virus (RadLV)-transformed cell line derived from C57BL/6 mice. The library was first screened using the H-2III (5') probe, which detects Class I genes of the H-2 complex. In the primary screening 163 H-2III positives were isolated. The H-2III-positive isolates were then hybridized with an AKR-derived virus probe, EcoB/S, which contains sequences from both the pol and the env genes of the virus. Nine virus-positive isolates were detected. Localization of these cosmid isolates containing viral sequences within the H-2 complex was done utilizing low-copy probes and confirmed using previously mapped cosmid isolates from other laboratories. We report here the isolation and characterization of VL30-like elements from the Qa and D regions of the MHC of several inbred mouse strains.

摘要

我们实验室之前的研究在一系列跨越正常C57BL/10小鼠主要组织相容性复合体(MHC)TL区域的黏粒中描述了两个内源性前病毒样序列。这些病毒中至少有一个与VL30元件有相似之处。为了确定MHC中是否整合了其他VL30样逆转录病毒元件,我们使用来自C57BL/6小鼠的辐射白血病病毒(RadLV)转化细胞系的DNA构建了一个黏粒文库。该文库首先用H-2III(5')探针进行筛选,该探针可检测H-2复合体的I类基因。在初次筛选中,分离出163个H-2III阳性克隆。然后将H-2III阳性克隆与源自AKR的病毒探针EcoB/S杂交,该探针包含病毒pol和env基因的序列。检测到9个病毒阳性克隆。利用低拷贝探针确定这些含有病毒序列的黏粒克隆在H-2复合体内的定位,并使用其他实验室先前定位的黏粒克隆进行了确认。我们在此报告从几种近交小鼠品系的MHC的Qa和D区域分离和鉴定VL30样元件的情况。

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