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本文引用的文献

1
The exogenous form of Jaagsiekte retrovirus is specifically associated with a contagious lung cancer of sheep.绵羊肺腺瘤逆转录病毒的外源性形式与绵羊的一种传染性肺癌特别相关。
J Virol. 1996 Mar;70(3):1618-23. doi: 10.1128/JVI.70.3.1618-1623.1996.
2
Mutation of the C/EBP binding sites in the Rous sarcoma virus long terminal repeat and gag enhancers.劳氏肉瘤病毒长末端重复序列和gag增强子中C/EBP结合位点的突变
J Virol. 1993 May;67(5):2862-70. doi: 10.1128/JVI.67.5.2862-2870.1993.
3
PCR amplification of up to 35-kb DNA with high fidelity and high yield from lambda bacteriophage templates.从λ噬菌体模板中以高保真度和高产量进行高达35千碱基DNA的PCR扩增。
Proc Natl Acad Sci U S A. 1994 Mar 15;91(6):2216-20. doi: 10.1073/pnas.91.6.2216.
4
The VBP and a1/EBP leucine zipper factors bind overlapping subsets of avian retroviral long terminal repeat CCAAT/enhancer elements.VBP和a1/EBP亮氨酸拉链因子与禽逆转录病毒长末端重复CCAAT/增强子元件的重叠亚集结合。
J Virol. 1994 Oct;68(10):6232-42. doi: 10.1128/JVI.68.10.6232-6242.1994.
5
Analysis of a type D retroviral capsid gene expressed in ovine pulmonary carcinoma and present in both affected and unaffected sheep genomes.对在绵羊肺癌中表达且存在于患病和未患病绵羊基因组中的D型逆转录病毒衣壳基因的分析。
Virology. 1994 Jul;202(1):480-4. doi: 10.1006/viro.1994.1366.
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Multiple forms of C/EBP beta bind the EFII enhancer sequence in the Rous sarcoma virus long terminal repeat.多种形式的C/EBPβ结合劳氏肉瘤病毒长末端重复序列中的EFII增强子序列。
Mol Cell Biol. 1994 Jul;14(7):4855-71. doi: 10.1128/mcb.14.7.4855-4871.1994.
7
Recovery of virtually full-length HIV-1 provirus of diverse subtypes from primary virus cultures using the polymerase chain reaction.使用聚合酶链反应从原代病毒培养物中回收多种亚型的几乎全长的HIV-1前病毒。
Virology. 1995 Oct 20;213(1):80-6. doi: 10.1006/viro.1995.1548.
8
Aetiology of jaagsiekte: experimental transmission to lambs by means of cultured cells and cell homogenates.羊肺腺瘤病的病因:通过培养细胞和细胞匀浆向羔羊进行实验性传播。
Onderstepoort J Vet Res. 1980 Mar;47(1):13-8.
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Determination of the leukaemogenicity of a murine retrovirus by sequences within the long terminal repeat.通过长末端重复序列内的序列测定鼠逆转录病毒的致白血病性。
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10
Thymotropism of murine leukemia virus is conferred by its long terminal repeat.鼠白血病病毒的亲胸腺性由其长末端重复序列赋予。
Proc Natl Acad Sci U S A. 1983 Jul;80(14):4203-7. doi: 10.1073/pnas.80.14.4203.

独特的长末端重复序列U3可将与绵羊肺癌相关的外源性绵羊肺腺瘤逆转录病毒与绵羊基因组中的内源性基因座区分开来。

Unique long terminal repeat U3 sequences distinguish exogenous jaagsiekte sheep retroviruses associated with ovine pulmonary carcinoma from endogenous loci in the sheep genome.

作者信息

Bai J, Zhu R Y, Stedman K, Cousens C, Carlson J, Sharp J M, DeMartini J C

机构信息

Department of Pathology, Colorado State University, Fort Collins 80523, USA.

出版信息

J Virol. 1996 May;70(5):3159-68. doi: 10.1128/JVI.70.5.3159-3168.1996.

DOI:10.1128/JVI.70.5.3159-3168.1996
PMID:8627796
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC190179/
Abstract

Ovine pulmonary carcinoma (OPC) is a contagious lung cancer of sheep that is presumed to be caused by an exogenous retrovirus of sheep, jaagsiekte sheep retrovirus (JSRV). The sheep genome carries 15 to 20 copies of endogenous sheep retrovirus (ESRV) loci that hybridize to JSRV DNA probes. In order to clarity the etiologic roles of ESRV and an exogenous JSRV-like retrovirus (exJSRV) in OPC, we assessed sequence differences between ESRV and JSRV. Molecular characterization of six ESRV loci revealed restriction sites specific for JSRV. Nucleotide sequences of ESRVs from sheep of different breeds were similar to those of JSRV in structural genes but divergent in U3. Therefore, primers specific for the U3 sequences of exJSRV were designed for use in the PCR. Of 13 tumor DNAs tested by PCR with these exogenous-virus U3 primers, 8 produced DNA fragments that hybridized with the JSRV gag probe, but neither lung DNAs from healthy sheep nor DNAs from nontumor tissues of diseased sheep produced similar DNA fragments. exJSRV PCR products from tumor DNAs of sheep with OPC from three continents had restriction profiles similar to each other but different from those of ESRVs upon digestion with EcoRI, HindIII, NdeI, KpnI, and ScaI. These exjSRVs could be classified into two genotypes according to U3 sequences and restriction profiles. U3 sequences of exJSRV proviruses in tumors strongly resembled those of JSRV but differed from those of ESRVs, suggesting that exJSRVs, rather than ESRVs, are primarily associated with oncogenesis in OPC.

摘要

绵羊肺癌(OPC)是一种绵羊的传染性肺癌,据推测是由绵羊的一种外源性逆转录病毒——绵羊肺腺瘤逆转录病毒(JSRV)引起的。绵羊基因组携带15至20个内源性绵羊逆转录病毒(ESRV)基因座,这些基因座可与JSRV DNA探针杂交。为了阐明ESRV和一种外源性JSRV样逆转录病毒(exJSRV)在OPC中的病因学作用,我们评估了ESRV和JSRV之间的序列差异。六个ESRV基因座的分子特征揭示了JSRV特有的限制性酶切位点。来自不同品种绵羊的ESRV核苷酸序列在结构基因上与JSRV相似,但在U3区域存在差异。因此,设计了针对exJSRV U3序列的引物用于PCR。在用这些外源性病毒U3引物进行PCR检测的13个肿瘤DNA中,有8个产生了与JSRV gag探针杂交的DNA片段,但健康绵羊的肺DNA和患病绵羊的非肿瘤组织DNA均未产生类似的DNA片段。来自三大洲患有OPC的绵羊肿瘤DNA的exJSRV PCR产物在用EcoRI、HindIII、NdeI、KpnI和ScaI消化后的限制性酶切图谱彼此相似,但与ESRV的不同。根据U3序列和限制性酶切图谱,这些exJSRV可分为两种基因型。肿瘤中exJSRV前病毒的U3序列与JSRV的非常相似,但与ESRV的不同,这表明exJSRV而非ESRV主要与OPC的肿瘤发生有关。