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两种剪接的单纯疱疹病毒1型立即早期mRNA的结构,它们定位于病毒DNA S成分的独特区域与重复区域的交界处。

Structures of two spliced herpes simplex virus type 1 immediate-early mRNA's which map at the junctions of the unique and reiterated regions of the virus DNA S component.

作者信息

Watson R J, Sullivan M, Vande Woude G F

出版信息

J Virol. 1981 Jan;37(1):431-44. doi: 10.1128/JVI.37.1.431-444.1981.

DOI:10.1128/JVI.37.1.431-444.1981
PMID:6260993
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC171020/
Abstract

We have examined the structures of two herpes simplex virus type 1 immediate-early (IE) RNAs (IE mRNA-4 and IE mRNA-5) which map at the junctions of the unique (Us) and reiterated regions (TRs/IRs) of the virus DNA short component. Hybrids between IE cytoplasmic RNA and herpes simplex virus type 1 DNA restriction fragments were digested with single-strand-specific nucleases S1 and exonuclease VII, and the products were analyzed by agarose gel electrophoresis. Data obtained with the nuclease digestion technique were confirmed by electron microscopy of R-loop structures formed with polyadenylated IE RNA and virus DNA fragments. It was found that both IE mRNA-4 and IE mRNA-5 contained a 260-base 5'-terminal cotranscript which mapped at equivalent loci within TRs/IRs. These 5'-terminal sequences were shown to be spliced to 3'-terminal cotranscripts of 1,450 bases (for IE mRNA-4) and 1,540 bases (for IE mRNA-5). The 3'-terminal cotranscripts contained sequences encoded by both TRs/IRs and opposite ends of Us, indicating that the introns contained by the IE mRNA-4 and IE mRNA-5 genes, found to be approximately 150 base pairs in size, mapped entirely within the reiterated sequences. The data suggest that these genes may contain common and unique components, and the implications of this model are discussed.

摘要

我们研究了两种1型单纯疱疹病毒即刻早期(IE)RNA(IE mRNA - 4和IE mRNA - 5)的结构,它们位于病毒DNA短组分的独特(Us)和重复区域(TRs/IRs)的交界处。用单链特异性核酸酶S1和核酸外切酶VII消化IE细胞质RNA与1型单纯疱疹病毒DNA限制性片段之间的杂交体,并通过琼脂糖凝胶电泳分析产物。通过对聚腺苷酸化的IE RNA和病毒DNA片段形成的R环结构进行电子显微镜观察,证实了核酸酶消化技术获得的数据。发现IE mRNA - 4和IE mRNA - 5都含有一个260个碱基的5'端共转录本,其位于TRs/IRs内的等效位点。这些5'端序列被证明与1450个碱基(对于IE mRNA - 4)和1540个碱基(对于IE mRNA - 5)的3'端共转录本进行了剪接。3'端共转录本包含由TRs/IRs和Us的相对末端编码的序列,表明IE mRNA - 4和IE mRNA - 5基因所含的内含子大小约为150个碱基对,完全位于重复序列内。数据表明这些基因可能包含共同和独特的组分,并讨论了该模型的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a49/171020/c170ee74a9c6/jvirol00001-0461-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a49/171020/749093bdc020/jvirol00001-0454-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a49/171020/96632ce64a27/jvirol00001-0455-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a49/171020/506faa6ed914/jvirol00001-0456-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a49/171020/83e065876669/jvirol00001-0457-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a49/171020/8c614444b858/jvirol00001-0458-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a49/171020/4df2941ec641/jvirol00001-0459-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a49/171020/135db930283e/jvirol00001-0461-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a49/171020/c170ee74a9c6/jvirol00001-0461-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a49/171020/749093bdc020/jvirol00001-0454-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a49/171020/96632ce64a27/jvirol00001-0455-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a49/171020/506faa6ed914/jvirol00001-0456-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a49/171020/83e065876669/jvirol00001-0457-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a49/171020/8c614444b858/jvirol00001-0458-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a49/171020/4df2941ec641/jvirol00001-0459-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a49/171020/135db930283e/jvirol00001-0461-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a49/171020/c170ee74a9c6/jvirol00001-0461-b.jpg

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Structures of two spliced herpes simplex virus type 1 immediate-early mRNA's which map at the junctions of the unique and reiterated regions of the virus DNA S component.两种剪接的单纯疱疹病毒1型立即早期mRNA的结构,它们定位于病毒DNA S成分的独特区域与重复区域的交界处。
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A herpes simplex virus type 1 function continuously required for early and late virus RNA synthesis.一种单纯疱疹病毒1型功能,早期和晚期病毒RNA合成持续需要该功能。
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单纯疱疹病毒1型的U(S)3蛋白激酶可阻断由U(S)1.5和U(L)13基因产物诱导的半胱天冬酶3激活,并以细胞类型特异性方式调节转导的U(S)1.5开放阅读框的表达。
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Small dense nuclear bodies are the site of localization of herpes simplex virus 1 U(L)3 and U(L)4 proteins and of ICP22 only when the latter protein is present.小而致密的核体是单纯疱疹病毒1型U(L)3和U(L)4蛋白以及仅当存在ICP22蛋白时其定位的位点。
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