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本文引用的文献

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Murine endogenous retroviruses and their transcriptional potentials.小鼠内源性逆转录病毒及其转录潜能。
Mamm Genome. 2004 Nov;15(11):914-23. doi: 10.1007/s00335-004-2409-x.
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Intrinsic immunity: a front-line defense against viral attack.固有免疫:抵御病毒攻击的一线防御
Nat Immunol. 2004 Nov;5(11):1109-15. doi: 10.1038/ni1125.
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Molecular cloning, complete sequence, and biological characterization of a xenotropic murine leukemia virus constitutively released from the human B-lymphoblastoid cell line DG-75.从人B淋巴母细胞系DG-75中持续释放的嗜异性鼠白血病病毒的分子克隆、全序列及生物学特性分析
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A virus-virus interaction circumvents the virus receptor requirement for infection by pathogenic retroviruses.一种病毒与病毒之间的相互作用规避了致病性逆转录病毒感染所需的病毒受体。
J Virol. 2003 Mar;77(6):3460-9. doi: 10.1128/jvi.77.6.3460-3469.2003.
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Wild mice: an ever-increasing contribution to a popular mammalian model.野生小鼠:对一种广受欢迎的哺乳动物模型的贡献日益增加。
Trends Genet. 2003 Jan;19(1):24-31. doi: 10.1016/s0168-9525(02)00007-0.
6
Receptor usage and fetal expression of ovine endogenous betaretroviruses: implications for coevolution of endogenous and exogenous retroviruses.绵羊内源性β逆转录病毒的受体使用情况及胎儿表达:对内源性和外源性逆转录病毒共同进化的影响
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7
Characterization of a polytropic murine leukemia virus proviral sequence associated with the virus resistance gene Rmcf of DBA/2 mice.与DBA/2小鼠的病毒抗性基因Rmcf相关的多嗜性鼠白血病病毒前病毒序列的特征分析。
J Virol. 2002 Aug;76(16):8218-24. doi: 10.1128/jvi.76.16.8218-8224.2002.
8
Genetic control of a mouse serum lipoprotein factor that inactivates murine leukemia viruses: evaluation of apolipoprotein F as a candidate.一种可使鼠白血病病毒失活的小鼠血清脂蛋白因子的遗传控制:载脂蛋白F作为候选因子的评估。
J Virol. 2002 Mar;76(5):2279-86. doi: 10.1128/jvi.76.5.2279-2286.2002.
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Fv-4: identification of the defect in Env and the mechanism of resistance to ecotropic murine leukemia virus.Fv-4:Env缺陷的鉴定及对嗜亲性鼠白血病病毒的抗性机制
J Virol. 2001 Nov;75(22):11244-8. doi: 10.1128/JVI.75.22.11244-11248.2001.
10
Mink cell focus-forming murine leukemia virus killing of mink cells involves apoptosis and superinfection.水貂细胞病灶形成型鼠白血病病毒对水貂细胞的杀伤涉及细胞凋亡和超感染。
J Virol. 2001 Jul;75(13):6007-15. doi: 10.1128/JVI.75.13.6007-6015.2001.

Rmcf2是亚洲小鼠物种栗色小鼠中的一种嗜异性前病毒,可阻断多嗜性小鼠γ逆转录病毒的感染。

Rmcf2, a xenotropic provirus in the Asian mouse species Mus castaneus, blocks infection by polytropic mouse gammaretroviruses.

作者信息

Wu Tiyun, Yan Yuhe, Kozak Christine A

机构信息

Laboratory of Molecular Microbiology, National Institute and Allergy and Infectious Diseases, Bethesda, MD 20892-0460, USA.

出版信息

J Virol. 2005 Aug;79(15):9677-84. doi: 10.1128/JVI.79.15.9677-9684.2005.

DOI:10.1128/JVI.79.15.9677-9684.2005
PMID:16014929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1181588/
Abstract

Cells from the Asian wild mouse species Mus castaneus are resistant to infection by the polytropic host range group of mouse gammaretroviruses. Two factors are responsible for this resistance: a defective XPR1 cell surface receptor for polytropic murine leukemia viruses (P-MLVs), and a resistance factor detectable only in interspecies hybrids between M. castaneus and mice with an XPR1 variant that permits infection by xenotropic MLVs (X-MLVs) as well as P-MLVs. This second novel virus resistance phenotype has been associated with expression of viral Env glycoprotein; Northern blotting with specific hybridization probes identified a spliced X-MLV env message unique to virus-resistant mice. These observations suggest that resistance is due to expression of one or more endogenous X-MLV envelope genes that interfere with infection by exogenous P-MLVs. M. castaneus contains multiple X-MLV proviruses, but serial backcrosses reduced this proviral content and permitted identification of a single proviral env sequence inherited with resistance. The resistance phenotype and the provirus were mapped to the same site on distal chromosome 18. The provirus was shown to be a full-length provirus highly homologous to previously described X-MLVs. Use of viral pseudotypes confirmed that this resistance gene, termed Rmcf2, prevents entry of P-MLVs. Rmcf2 resembles the virus resistance genes Fv4 and Rmcf in that it produces Env glycoprotein but fails to produce infectious virus; the proviruses associated with all three resistance genes have fatal defects. This type of provirus Env-mediated resistance represents an important defense mechanism in wild mouse populations exposed to endemic infections.

摘要

亚洲野生小鼠物种栗褐家鼠(Mus castaneus)的细胞对多嗜性宿主范围组的小鼠γ逆转录病毒感染具有抗性。这种抗性由两个因素导致:多嗜性鼠白血病病毒(P-MLVs)的XPR1细胞表面受体存在缺陷,以及一种抗性因子,该因子仅在栗褐家鼠与具有允许异嗜性MLVs(X-MLVs)以及P-MLVs感染的XPR1变体的小鼠之间的种间杂交后代中可检测到。这种第二种新型病毒抗性表型与病毒Env糖蛋白的表达有关;用特异性杂交探针进行的Northern印迹法鉴定出一种仅在病毒抗性小鼠中存在的剪接X-MLV env信息。这些观察结果表明,抗性是由于一个或多个内源性X-MLV包膜基因的表达,这些基因干扰了外源性P-MLVs的感染。栗褐家鼠含有多个X-MLV前病毒,但连续回交减少了这种前病毒含量,并使得能够鉴定出与抗性一起遗传的单个前病毒env序列。抗性表型和前病毒被定位到18号染色体远端的同一位点。该前病毒被证明是一个与先前描述的X-MLVs高度同源的全长前病毒。使用病毒假型证实,这个被称为Rmcf2的抗性基因可阻止P-MLVs进入。Rmcf2与病毒抗性基因Fv4和Rmcf相似,因为它产生Env糖蛋白但不产生感染性病毒;与所有这三个抗性基因相关的前病毒都有致命缺陷。这种由前病毒Env介导的抗性类型代表了野生小鼠群体中抵御地方性感染的一种重要防御机制。