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Altered dynamics of scaRNA2 and scaRNA9 in response to stress correlates with disrupted nuclear organization

机译:响应压力而改变的scaRNA2和scaRNA9动力学与核组织受损有关

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Small Cajal body-specific RNAs (scaRNAs) are part of small Cajal body-specific ribonucleoproteins (scaRNPs) that modify small nuclear RNA (snRNA) in Cajal bodies (CBs). Several scaRNAs (scaRNA 2, 9 and 17) have been found to generate smaller, nucleolus-enriched fragments. We hypothesize that the fragments derived from scaRNA 2, 9 and 17 form regulatory RNPs that influence the level of modifications within rRNA by altering small nucleolar RNP (snoRNP) activity. Here we show that external factors such as DNA damaging agents can alter the scaRNA9 full length to processed fragment ratio. We also show that full-length scaRNA2 levels are likewise impacted by DNA damage, which correlates with the disruption of SMN, coilin and WRAP53 co-localization in CBs. The dynamics of scaRNA9 were also shown to be affected by Drosha levels, which suggests that this protein may participate in the biogenesis and processing of this non-coding RNA. Identification of factors that contribute to scaRNA 2, 9 and 17 processing may facilitate an assessment of how external stress can lead to changes in rRNA modifications.
机译:小Cajal身体特异性RNA(scaRNA)是小Cajal身体特异性核糖核蛋白(scaRNPs)的一部分,它们修饰Cajal身体(CBs)中的小核RNA(snRNA)。已发现几种scaRNA(scaRNA 2、9和17)可产生较小的,富含核仁的片段。我们假设源自scaRNA 2、9和17的片段形成调节性RNP,通过改变小核仁RNP(snoRNP)活性来影响rRNA内修饰的水平。在这里,我们显示外部因素(例如DNA破坏剂)可以改变scaRNA9全长与加工片段的比率。我们还显示,全长scaRNA2水平同样受到DNA损伤的影响,DNA损伤与CBs中SMN,线圈蛋白和WRAP53共定位的破坏有关。 scaRNA9的动力学也显示受Drosha水平的影响,这表明该蛋白可能参与该非编码RNA的生物发生和加工。鉴定有助于scaRNA 2、9和17加工的因素可能有助于评估外部压力如何导致rRNA修饰的变化。

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