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Analysis of adenovirus VA RNA(I) structure and stability using compensatory base pair modifications

机译:使用补偿碱基对修饰分析腺病毒VA RNA(I)的结构和稳定性

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摘要

Adenovirus VA RNAs are short non-coding transcripts that assist in maintaining viral protein expression in infected cells. Six sets of mismatch and compensatory base pair mutants of VA RNA(I) were examined by gel mobility and RNA UV melting to assess the contribution of each structural domain to its overall structure and stability. Each domain of VA RNA(I) was first assigned to one of two apparent unfolding transitions in the wild-type melting profile. The Terminal Stem and Central Domain unfold in a single cooperative apparent transition with an apparent T-m of similar to 60 degrees C. In contrast, the Apical Stem unfolds independently and with much higher apparent T-m of similar to 83 degrees C. Remarkably, this domain appears to behave as an almost entirely autonomous unit within the RNA, mirroring the functional division within the RNA between PKR binding and inhibition. The effects of mismatch and compensatory mutations at five of the six sites on the RNA melting profile are consistent with proposed base pairing and provide further validation of the current secondary structure model. Mutations in the Central Domain were tested in PKR inhibition assays and a component of the VA RNA(I) Central Domain structure essential for PKR inhibitory activity was identified.
机译:腺病毒VA RNA是短的非编码转录本,可帮助维持感染细胞中病毒蛋白的表达。通过凝胶迁移率和RNA UV熔解检查了六组VA RNA(I)的错配和补偿碱基对突变体,以评估每个结构域对其整体结构和稳定性的贡献。首先将VA RNA(I)的每个结构域分配给野生型熔解图谱中两个明显的未折叠转变之一。末端茎和中央结构域在单个协同表观过渡中展开,其表观Tm接近60摄氏度。相反,顶端茎独立地展开,并且表观Tm更高,近似于83摄氏度。充当RNA中几乎完全自治的单元,反映了PKR结合与抑制之间RNA的功能划分。 RNA熔解图谱上六个位点中五个位点的错配和补偿突变的影响与拟议的碱基配对一致,并提供了当前二级结构模型的进一步验证。在PKR抑制试验中测试了Central Domain中的突变,并鉴定了PKR抑制活性所必需的VA RNA(I)Central Domain结构的组成部分。

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