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对辛德毕斯病毒缺陷干扰RNA的研究,这些RNA的5'末端有或没有天冬氨酸转运RNA(tRNAAsp)序列。

Studies of defective interfering RNAs of Sindbis virus with and without tRNAAsp sequences at their 5' termini.

作者信息

Tsiang M, Monroe S S, Schlesinger S

出版信息

J Virol. 1985 Apr;54(1):38-44. doi: 10.1128/JVI.54.1.38-44.1985.

Abstract

Three of six independently derived defective interfering (DI) particles of Sindbis virus generated by high-multiplicity passaging in cultured cells have tRNAAsp sequences at the 5' terminus of their RNAs (Monroe and Schlesinger, J. Virol. 49:865-872, 1984). In the present work, we found that the 5'-terminal sequences of the three tRNAAsp-negative DI RNAs were all derived from viral genomic RNA. One DI RNA sample had the same 5'-terminal sequence as the standard genome. The DI RNAs from another DI particle preparation were heterogeneous at the 5' terminus, with the sequence being either that of the standard 5' end or rearrangements of regions near the 5' end. The sequence of the 5' terminus of the third DI RNA sample consisted of the 5' terminus of the subgenomic 26S mRNA with a deletion from nucleotides 24 to 67 of the 26S RNA sequence. These data showed that the 5'-terminal nucleotides can undergo extensive variations and that the RNA is still replicated by virus-specific enzymes. DI RNAs of Sindbis virus evolve from larger to smaller species. In the two cases in which we followed the evolution of DI RNAs, the appearance of tRNAAsp-positive molecules occurred at the same time as did the emergence of the smaller species of DI RNAs. In pairwise competition experiments, one of the tRNAAsp-positive DI RNAs proved to be the most effective DI RNA, but under identical conditions, a second tRNAAsp-positive DI RNA was unable to compete with the tRNAAsp-negative DIs. Therefore, the tRNAAsp sequence at the 5' terminus of a Sindbis DI RNA is not the primary factor in determining which DI RNA becomes the predominant species in a population of DI RNA molecules.

摘要

通过在培养细胞中高倍传代产生的辛德毕斯病毒的六个独立衍生的缺陷干扰(DI)颗粒中,有三个在其RNA的5'末端具有tRNAAsp序列(门罗和施莱辛格,《病毒学杂志》49:865 - 872,1984)。在本研究中,我们发现三个tRNAAsp阴性DI RNA的5'末端序列均源自病毒基因组RNA。一个DI RNA样本具有与标准基因组相同的5'末端序列。来自另一种DI颗粒制剂的DI RNA在5'末端是异质的,其序列要么是标准5'末端的序列,要么是5'末端附近区域的重排。第三个DI RNA样本的5'末端序列由亚基因组26S mRNA的5'末端组成,26S RNA序列的核苷酸24至67处有缺失。这些数据表明5'末端核苷酸可发生广泛变异,并且RNA仍由病毒特异性酶复制。辛德毕斯病毒的DI RNA从较大的种类进化为较小的种类。在我们追踪DI RNA进化的两个案例中,tRNAAsp阳性分子的出现与较小种类的DI RNA的出现同时发生。在成对竞争实验中,其中一个tRNAAsp阳性DI RNA被证明是最有效的DI RNA,但在相同条件下,第二个tRNAAsp阳性DI RNA无法与tRNAAsp阴性DI竞争。因此,辛德毕斯DI RNA 5'末端的tRNAAsp序列不是决定哪种DI RNA在DI RNA分子群体中成为优势种类的主要因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46b5/254757/ebe824bfb1f6/jvirol00121-0049-a.jpg

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