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克雅氏病中的潜在逆转录病毒RNA。

Potential retroviral RNAs in Creutzfeldt-Jakob disease.

作者信息

Murdoch G H, Sklaviadis T, Manuelidis E E, Manuelidis L

机构信息

Section of Neuropathology, Yale Medical School, New Haven, Connecticut 06510.

出版信息

J Virol. 1990 Apr;64(4):1477-86. doi: 10.1128/JVI.64.4.1477-1486.1990.

Abstract

The molecular nature of the related infectious agents that cause Creutzfeldt-Jakob disease (CJD) and scrapie is poorly understood, and an agent-specific nucleic acid genome has not yet been identified. Several biological manifestations of these agents resemble those seen in retrovirus-induced diseases. We therefore attempted to identify an agent-specific retrovirus-like RNA transcript in CJD infectious fractions. A series of synthetic oligonucleotides complementary to known mammalian retroviral primer binding sites were used in a primer extension assay. Substrate nucleic acids isolated from partially purified hamster brain CJD infectious fractions and from parallel normal brain fractions were compared with total starting brain RNA. This sensitive exogenous strong-stop reaction revealed that CJD infectious fractions contained a series of potential retroviral RNAs including apparent transcripts of endogenous hamster IAP genes. Most transcripts selectively recovered in the fractions were substantially protected from micrococcal nuclease digestion, and at least one substrate RNA, consistent with an intracisternal A particle, was packaged in a form that had the same buoyant density as CJD infectivity. Although a completely CJD-specific transcript was not identified, the copurification of potential retroviral transcripts with CJD infectivity suggests that models of disease involving retrovirus-like nucleic acid elements deserve further consideration.

摘要

导致克雅氏病(CJD)和羊瘙痒症的相关感染因子的分子本质仍知之甚少,且尚未鉴定出因子特异性核酸基因组。这些因子的一些生物学表现类似于逆转录病毒诱导疾病中所观察到的表现。因此,我们试图在CJD感染组分中鉴定一种因子特异性的类逆转录病毒RNA转录本。在引物延伸试验中使用了一系列与已知哺乳动物逆转录病毒引物结合位点互补的合成寡核苷酸。将从部分纯化的仓鼠脑CJD感染组分和平行的正常脑组分中分离的底物核酸与起始脑总RNA进行比较。这种灵敏的外源强终止反应表明,CJD感染组分含有一系列潜在的逆转录病毒RNA,包括仓鼠内源性IAP基因的明显转录本。在这些组分中选择性回收的大多数转录本基本上免受微球菌核酸酶消化的影响,并且至少一种与脑池内A颗粒一致的底物RNA以与CJD感染性相同的浮力密度形式被包装。虽然未鉴定出完全CJD特异性的转录本,但潜在的逆转录病毒转录本与CJD感染性的共纯化表明,涉及类逆转录病毒核酸元件的疾病模型值得进一步考虑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0777/249281/e861fa78e1ae/jvirol00059-0071-a.jpg

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