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禽肉瘤/白血病病毒3'非翻译区的点突变导致包装缺陷。

Point mutations in the avian sarcoma/leukosis virus 3' untranslated region result in a packaging defect.

作者信息

Aschoff J M, Foster D, Coffin J M

机构信息

Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts 02111, USA.

出版信息

J Virol. 1999 Sep;73(9):7421-9. doi: 10.1128/JVI.73.9.7421-7429.1999.

Abstract

The 3' untranslated region (3' UTR) between the 3' end of env and the long terminal repeat is well conserved among avian retroviruses and is essential for efficient replication. Deletion of the dr1 element within the 3' UTR has been reported to have various effects, including reduced levels of unspliced RNA in the cytoplasm, decreased stability of unspliced RNA, decreased particle production, and decreased genomic RNA packaging. To probe the role of specific sequences within dr1 in virus replication, site-directed mutagenesis was utilized to perturb parts of the predicted secondary structure of dr1. Seven of thirteen mutations had no significant effect; the others resulted in an approximately 10- to 20-fold reduction in replication. These mutants were further characterized and found to impair cytoplasmic accumulation of unspliced RNA only slightly. Furthermore, no decreases were observed in the stability of the unspliced RNA or in the production of virus particles. Genomic RNA packaging, however, was reduced by about 10-fold. Similar amounts of particles were produced by cells containing the mutant and wild-type DNA, and all particles contained similar levels of reverse transcriptase activity. The results suggest that the region of the dr1 disrupted by the mutations plays a role in genomic RNA packaging, although that packaging may not be the only role for dr1.

摘要

env基因3'端与长末端重复序列之间的3'非翻译区(3'UTR)在禽逆转录病毒中高度保守,对高效复制至关重要。据报道,3'UTR内dr1元件的缺失具有多种影响,包括细胞质中未剪接RNA水平降低、未剪接RNA稳定性下降、病毒粒子产生减少以及基因组RNA包装减少。为了探究dr1内特定序列在病毒复制中的作用,利用定点诱变扰乱dr1预测二级结构的部分区域。13个突变中有7个没有显著影响;其他突变导致复制减少约10至20倍。对这些突变体进行进一步表征,发现它们仅轻微损害未剪接RNA的细胞质积累。此外,未观察到未剪接RNA稳定性或病毒粒子产生的降低。然而,基因组RNA包装减少了约10倍。含有突变体和野生型DNA的细胞产生的病毒粒子数量相似,并且所有粒子都含有相似水平的逆转录酶活性。结果表明,被突变破坏的dr1区域在基因组RNA包装中起作用,尽管这种包装可能不是dr1的唯一作用。

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