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本文引用的文献

1
Targeted disruption of the alpha1,3-galactosyltransferase gene in cloned pigs.克隆猪中α1,3-半乳糖基转移酶基因的靶向破坏。
Nat Biotechnol. 2002 Mar;20(3):251-5. doi: 10.1038/nbt0302-251.
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Porcine endogenous retrovirus transmission characteristics of an inbred herd of miniature swine.小型猪近交群体中猪内源性逆转录病毒的传播特征
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Characterization of chromosomally assigned replication-competent gamma porcine endogenous retroviruses derived from a large white pig and expression in human cells.源自大白猪的染色体定位的具有复制能力的γ型猪内源性逆转录病毒的特性及其在人细胞中的表达
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Production of alpha-1,3-galactosyltransferase knockout pigs by nuclear transfer cloning.通过核移植克隆生产α-1,3-半乳糖基转移酶基因敲除猪。
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Identification of a novel type C porcine endogenous retrovirus: evidence that copy number of endogenous retroviruses increases during host inbreeding.一种新型C型猪内源性逆转录病毒的鉴定:宿主近亲繁殖过程中内源性逆转录病毒拷贝数增加的证据。
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The porcine endogenous retrovirus long terminal repeat contains a single nucleotide polymorphism that confers distinct differences in estrogen receptor binding affinity between PERV A and PERV B/C subtypes.猪内源性逆转录病毒长末端重复序列包含一个单核苷酸多态性,该多态性导致PERV A和PERV B/C亚型在雌激素受体结合亲和力上存在明显差异。
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The number of a U3 repeat box acting as an enhancer in long terminal repeats of polytropic replication-competent porcine endogenous retroviruses dynamically fluctuates during serial virus passages in human cells.在多嗜性具有复制能力的猪内源性逆转录病毒的长末端重复序列中,作为增强子的U3重复框数量在人细胞中连续病毒传代过程中动态波动。
J Virol. 2001 Aug;75(15):6933-40. doi: 10.1128/JVI.75.15.6933-6940.2001.
8
Multiple groups of novel retroviral genomes in pigs and related species.猪及相关物种中的多组新型逆转录病毒基因组。
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9
Antiretroviral agents inhibit infection of human cells by porcine endogenous retroviruses.抗逆转录病毒药物可抑制猪内源性逆转录病毒对人类细胞的感染。
Antimicrob Agents Chemother. 2000 Dec;44(12):3432-3. doi: 10.1128/AAC.44.12.3432-3433.2000.
10
Xenotransplantation: reappraising the risk of retroviral zoonosis.异种移植:重新评估逆转录病毒人畜共患病的风险。
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异三聚体蛋白复合物NF-Y对猪源及感染人细胞释放的猪内源性逆转录病毒的转录调控以及免疫抑制药物的影响

Transcriptional regulation of porcine endogenous retroviruses released from porcine and infected human cells by heterotrimeric protein complex NF-Y and impact of immunosuppressive drugs.

作者信息

Scheef Gregor, Fischer Nicole, Flory Egbert, Schmitt Isabel, Tönjes Ralf R

机构信息

Paul-Ehrlich-Institut, Paul-Ehrlich-Strasse 51-59, D-63225 Langen, Germany.

出版信息

J Virol. 2002 Dec;76(24):12553-63. doi: 10.1128/jvi.76.24.12553-12563.2002.

DOI:10.1128/jvi.76.24.12553-12563.2002
PMID:12438581
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC136706/
Abstract

Recent studies revealed a significant promoter activity of porcine endogenous retrovirus (PERV) long terminal repeats (LTRs) in different human and mammalian cell lines, which is mediated by a 39-bp repeat located in the U3 region in different numbers, representing an enhancer (G. Scheef, N. Fischer, U. Krach, and R. R. Tönjes, J. Virol. 75:6933-6940, 2001). A statistical transcription factor analysis revealed putative binding sites for the CCAAT-binding transcription factor NF-Y inside the 39-bp repeat. Specific binding of NF-Y to the repeat sequence was demonstrated by electrophoretic mobility shift assays and supershift assays with specific antibodies directed against the three subunits of NF-Y. To identify further transcription-regulating elements, genetically modified LTRs lacking the repeat box, U3, R, or U5 were investigated. The results indicated a strong inhibitory element in the R region, as the deletion of R caused a significantly increased promoter activity. Since PERV might play a potential role in the application of xenogeneic cell therapy and xenotransplantation techniques, we have investigated whether immunosuppressive drugs that are routinely used in transplantation medicine have an impact on the promoter activity. Neither cyclosporine nor prednisolone had any influence on the promoter strength of the PERV LTRs. By performing a real-time PCR we were able to compare the proviral loads of porcine and infected human cells as well as the amount of released virions, which revealed a direct link between LTR activity and the number of released retroviruses.

摘要

最近的研究表明,猪内源性逆转录病毒(PERV)长末端重复序列(LTR)在不同的人类和哺乳动物细胞系中具有显著的启动子活性,这是由位于U3区域的不同数量的39bp重复序列介导的,该重复序列代表一种增强子(G. Scheef、N. Fischer、U. Krach和R. R. Tönjes,《病毒学杂志》75:6933 - 6940,2001年)。一项统计转录因子分析揭示了39bp重复序列内CCAAT结合转录因子NF-Y的推定结合位点。通过电泳迁移率变动分析和针对NF-Y三个亚基的特异性抗体进行的超迁移分析,证实了NF-Y与重复序列的特异性结合。为了鉴定更多的转录调控元件,研究了缺失重复框、U3、R或U5的基因修饰LTR。结果表明R区域存在一个强抑制元件,因为R的缺失导致启动子活性显著增加。由于PERV可能在异种细胞治疗和异种移植技术的应用中发挥潜在作用,我们研究了移植医学中常规使用的免疫抑制药物是否对启动子活性有影响。环孢素和泼尼松龙对PERV LTRs的启动子强度均无任何影响。通过进行实时PCR,我们能够比较猪细胞和感染人类细胞的前病毒载量以及释放的病毒粒子数量,这揭示了LTR活性与释放的逆转录病毒数量之间的直接联系。