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Purifying selection of long dsRNA is the first line of defense against false activation of innate immunity

机译:纯化长dsRNA的选择是抵抗先天免疫错误激活的第一道防线

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摘要

Detection of putative long dsRNA structure across transcriptomes. Transcriptomes of 49 organisms, from yeast to human, were analyzed. Using BLAST, we searched for long highly similar sequences within the same mRNA and pre-mRNA sequence. Reversely oriented sequences (red) are likely to pair and form a long intra-molecular dsRNA structure. As a natural control, we use same-strand tandem duplicated sequences (blue), which are not relevant to the secondary structure. For example, looking at the pre-mRNA of the human gene, multiple same-strand (blue) and inverted (red) matches are found, most of these pair together repetitive elements (orange) within introns (thin black line). In contrast, the mRNA molecule shows very few hits, all of them pair tandem sequences within repetitive elements in the 3′ UTR. Green bars represent A-to-I editing events, all of which are located in regions that have an inverted sequence match in the pre-mRNA
机译:跨转录组检测假定的长dsRNA结构。分析了从酵母到人的49种生物的转录组。使用BLAST,我们在相同的mRNA和前mRNA序列内搜索了高度相似的长序列。反向序列(红色)可能配对并形成一个长的分子内dsRNA结构。作为自然对照,我们使用同链串联重复序列(蓝色),该序列与二级结构无关。例如,观察人类基因的前mRNA,发现有多个相同链(蓝色)和反向(红色)的匹配,这些匹配中的大多数在内含子内(黑色细线)一起组成重复元件(橙色)。相比之下,mRNA分子显示的命中很少,它们都在3'UTR的重复元件中配对串联序列。绿条表示从A到I的编辑事件,所有这些事件均位于前mRNA中具有反向序列匹配的区域中

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