Thermodynamic and Phylogenetic Insights into hnRNP A1 Recognition of the HIV-1 Exon Splicing Silencer 3 Element

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• 作者：Carrie Rollins ; Jeffrey D. Levengood ; Brittany D. Rife ; Marco Salemi ; Blanton S. Tolbert
• 刊名：Biochemistry
• 出版年：2014
• 出版时间：April 8, 2014
• 年：2014
• 卷：53
• 期：13
• 页码：2172-2184
• 全文大小：681K
• 年卷期：v.53,no.13(April 8, 2014)
• ISSN：1520-4995

文摘

Complete expression of the HIV-1 genome requires balanced usage of suboptimal splice sites. The 3鈥?acceptor site A7 (ssA7) is negatively regulated in part by an interaction between the host hnRNP A1 protein and a viral splicing silencer (ESS3). Binding of hnRNP A1 to ESS3 and other upstream silencers is sufficient to occlude spliceosome assembly. Efforts to understand the splicing repressive properties of hnRNP A1 on ssA7 have revealed hnRNP A1 binds specific sites within the context of a highly folded RNA structure; however, biochemical models assert hnRNP A1 disrupts RNA structure through cooperative spreading. In an effort to improve our understanding of the ssA7 binding properties of hnRNP A1, herein we have performed a combined phylogenetic and biophysical study of the interaction of its UP1 domain with ESS3. Phylogenetic analyses of group M sequences (x̅ = 2860) taken from the Los Alamos HIV database reveal the ESS3 stem loop (SL3^ESS3) structure has been conserved throughout HIV-1 evolution, despite variations in primary sequence. Calorimetric titrations with UP1 clearly show the SL3^ESS3 structure is a critical binding determinant because deletion of the base-paired region reduces the affinity by 150-fold (K_d values of 27.8 nM and 4.2 渭M). Cytosine substitutions of conserved apical loop nucleobases show UP1 preferentially binds purines over pyrimidines, where site-specific interactions were detected via saturation transfer difference nuclear magnetic resonance. Chemical shift mapping of the UP1鈥揝L3^ESS3 interface by ¹H鈥?sup>15N heteronuclear single-quantum coherence spectroscopy titrations reveals a broad interaction surface on UP1 that encompasses both RRM domains and the inter-RRM linker. Collectively, our results describe a UP1 binding mechanism that is likely different from current models used to explain the alternative splicing properties of hnRNP A1.