Campbell L H, Borg K T, Haines J K, Moon R T, Schoenberg D R, Arrigo S J
Department of Microbiology and Immunology, Medical University of South Carolina, Charleston 29425-2230.
J Virol. 1994 Sep;68(9):5433-8. doi: 10.1128/JVI.68.9.5433-5438.1994.
In the absence of Rev or the Rev-responsive element, the Rev-dependent human immunodeficiency virus type 1 (HIV-1) RNAs do not behave as mRNAs; rather, they exhibit nuclear defects in splicing and/or nuclear export and cytoplasmic defects in stability and translation. A translational initiation factor, eIF-5A, has recently been shown to bind specifically to the Rev activation domain. As the binding of poly(A)-binding protein 1 (PAB1) to the poly(A) tail of mRNAs is involved in both the stability and translation of cytoplasmic mRNAs, we investigated whether Rev might influence the association of PAB1 with cytoplasmic HIV-1 RNAs. Antibodies were generated against PAB1. We used these antibodies in an immunoprecipitation assay to detect specific binding of PAB1 to cytoplasmic mRNAs. We found that in the presence of Rev, PAB1 was associated with Rev-dependent and Rev-independent RNAs in the cytoplasm of transfected cells. However, in the absence of functional Rev, we found little or no PAB1 associated with Rev-dependent RNAs. These RNAs were capable of binding PAB1 in vitro. These results demonstrate that HIV-1 RNAs are defective in PAB1 association in the absence of Rev.
在没有Rev或Rev反应元件的情况下,依赖Rev的1型人类免疫缺陷病毒(HIV-1)RNA不能作为mRNA发挥作用;相反,它们在剪接和/或核输出方面表现出核缺陷,在稳定性和翻译方面表现出细胞质缺陷。一种翻译起始因子,即真核翻译起始因子5A(eIF-5A),最近被证明能特异性结合Rev激活域。由于聚腺苷酸结合蛋白1(PAB1)与mRNA的聚腺苷酸尾结合参与细胞质mRNA的稳定性和翻译,我们研究了Rev是否可能影响PAB1与细胞质HIV-1 RNA的结合。制备了针对PAB1的抗体。我们在免疫沉淀试验中使用这些抗体来检测PAB1与细胞质mRNA的特异性结合。我们发现,在有Rev存在的情况下,PAB1与转染细胞细胞质中依赖Rev和不依赖Rev的RNA相关联。然而,在没有功能性Rev的情况下,我们发现很少或没有PAB1与依赖Rev的RNA相关联。这些RNA在体外能够结合PAB1。这些结果表明,在没有Rev的情况下,HIV-1 RNA在与PAB1结合方面存在缺陷。