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人腺病毒2型早期区域1B的组织:四种差异剪接mRNA的鉴定

Organization of early region 1B of human adenovirus type 2: identification of four differentially spliced mRNAs.

作者信息

Virtanen A, Pettersson U

出版信息

J Virol. 1985 May;54(2):383-91. doi: 10.1128/JVI.54.2.383-391.1985.

DOI:10.1128/JVI.54.2.383-391.1985
PMID:3989911
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC254808/
Abstract

The mRNAs from early region 1B of adenovirus type 2 have been studied by Northern blot, S1 nuclease, and cDNA analysis. Two novel mRNAs, designated 14S and 14.5S, have been observed in addition to the previously identified 9S, 13S, and 22S mRNAs. They are 1.26 and 1.31 kilobases long and differ from the 13S and 22S mRNAs in being composed of three exons instead of two. Their two terminal exons are the same as those present in the 13S mRNA, whereas the middle exon is unique to each of the two novel mRNA species. The structures of the 14S and 14.5S mRNAs allow the prediction of their coding capacities: both mRNA species, like the 22S and 13S mRNAs, contain an uninterrupted translational reading frame encoding a 21,000-molecular-weight (21K) polypeptide. The 14S mRNA can, in addition, encode a 16.5K polypeptide which shares N-terminal and C-terminal sequences with the 55K polypeptide, known to be encoded by the 22S mRNA. The 14.5S mRNA species encodes a hypothetical 9.2K polypeptide which has the same N terminus as the 55K polypeptide but a unique C terminus. The two mRNAs differ in their kinetics of appearance; the 14.5S mRNA is preferentially expressed late after infection in contrast to the 14S mRNA, which is present in approximately equal amounts early and late after infection. Taken together with previously published information the results suggest that early region 1B of adenovirus type 2 encodes five proteins in addition to virion polypeptide IX. These have predicted molecular weights of 55,000, 21,000, 16,500, 9,200, and 8,100.

摘要

利用Northern印迹法、S1核酸酶和cDNA分析法对2型腺病毒早期1B区的mRNA进行了研究。除了先前鉴定出的9S、13S和22S mRNA外,还观察到两种新的mRNA,分别命名为14S和14.5S。它们的长度分别为1.26和1.31千碱基,与13S和22S mRNA不同,由三个外显子组成而非两个。它们的两个末端外显子与13S mRNA中的相同,而中间外显子在这两种新的mRNA中各自独特。14S和14.5S mRNA的结构使其编码能力得以预测:这两种mRNA,与22S和13S mRNA一样,都含有一个不间断的翻译阅读框,编码一种分子量为21,000(21K)的多肽。此外,14S mRNA还可编码一种16.5K多肽,该多肽与已知由22S mRNA编码的55K多肽共享N端和C端序列。14.5S mRNA编码一种假定的9.2K多肽,其N端与55K多肽相同,但C端独特。这两种mRNA在出现动力学上有所不同;与14S mRNA不同,14.5S mRNA在感染后期优先表达,14S mRNA在感染早期和后期的含量大致相等。结合先前发表的信息,结果表明2型腺病毒早期1B区除了病毒体多肽IX外,还编码五种蛋白质。这些蛋白质的预测分子量分别为55,000、21,000、16,500、9,200和8,100。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f35/254808/d22132cc6895/jvirol00122-0154-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f35/254808/260047505e6b/jvirol00122-0151-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f35/254808/e7413b9c1c2d/jvirol00122-0152-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f35/254808/b92e0d11348b/jvirol00122-0152-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f35/254808/7f9c20b9a5ef/jvirol00122-0153-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f35/254808/68dec54b215f/jvirol00122-0153-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f35/254808/d22132cc6895/jvirol00122-0154-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f35/254808/260047505e6b/jvirol00122-0151-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f35/254808/e7413b9c1c2d/jvirol00122-0152-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f35/254808/b92e0d11348b/jvirol00122-0152-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f35/254808/7f9c20b9a5ef/jvirol00122-0153-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f35/254808/68dec54b215f/jvirol00122-0153-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f35/254808/d22132cc6895/jvirol00122-0154-a.jpg

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