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snoRNA a Novel Precursor of microRNA in Giardia lamblia

机译:snoRNA一种在贾第鞭毛虫中的微小RNA的新型前体

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摘要

An Argonaute homolog and a functional Dicer have been identified in the ancient eukaryote Giardia lamblia, which apparently lacks the ability to perform RNA interference (RNAi). The Giardia Argonaute plays an essential role in growth and is capable of binding specifically to the m7G-cap, suggesting a potential involvement in microRNA (miRNA)-mediated translational repression. To test such a possibility, small RNAs were isolated from Giardia trophozoites, cloned, and sequenced. A 26-nucleotide (nt) small RNA (miR2) was identified as a product of Dicer-processed snoRNA GlsR17 and localized to the cytoplasm by fluorescence in situ hybridization, whereas GlsR17 was found primarily in the nucleolus of only one of the two nuclei in Giardia. Three other small RNAs were also identified as products of snoRNAs, suggesting that the latter could be novel precursors of miRNAs in Giardia. Putative miR2 target sites were identified at the 3′-untranslated regions (UTR) of 22 variant surface protein mRNAs using the miRanda program. In vivo expression of Renilla luciferase mRNA containing six identical miR2 target sites in the 3′-UTR was reduced by 40% when co-transfected with synthetic miR2, while the level of luciferase mRNA remained unaffected. Thus, miR2 likely affects translation but not mRNA stability. This repression, however, was not observed when Argonaute was knocked down in Giardia using a ribozyme-antisense RNA. Instead, an enhancement of luciferase expression was observed, suggesting a loss of endogenous miR2-mediated repression when this protein is depleted. Additionally, the level of miR2 was significantly reduced when Dicer was knocked down. In all, the evidence indicates the presence of a snoRNA-derived miRNA-mediated translational repression in Giardia.
机译:在古代的真核生物贾第鞭毛虫中已鉴定出一种Argonaute同源物和一个功能性切丁酶,该菌显然缺乏进行RNA干扰(RNAi)的能力。贾第鞭毛虫(Giardia Argonaute)在生长中起着至关重要的作用,并且能够与m 7 G-cap特异性结合,表明可能参与了microRNA(miRNA)介导的翻译抑制。为了测试这种可能性,从贾第鞭毛虫滋养体中分离出小RNA,进行克隆和测序。 26核苷酸(nt)小RNA(miR2)被鉴定为Dicer处理的snoRNA GlsR17的产物,并通过荧光原位杂交定位于细胞质,而GlsR17主要存在于两个核中仅一个核的核仁中。贾第虫。 snoRNA的产物还鉴定出其他三个小RNA,这表明后者可能是贾第鞭毛虫中miRNA的新型前体。使用miRanda程序在22个变异表面蛋白mRNA的3'-非翻译区(UTR)上确定了miR2靶位点。当与合成miR2共转染时,在3'-UTR中含有六个相同miR2靶位点的海肾荧光素酶mRNA的体内表达降低了40%,而荧光素酶mRNA的水平仍然不受影响。因此,miR2可能会影响翻译,但不会影响mRNA的稳定性。但是,当使用核酶反义RNA在贾第鞭毛虫中将Argonaute击倒时,未观察到这种抑制。相反,观察到萤光素酶表达的增强,表明当该蛋白质耗尽时,内源性miR2介导的阻遏作用丧失。此外,当将Dicer敲低时,miR2的水平显着降低。总之,证据表明贾第鞭毛虫中存在snoRNA衍生的miRNA介导的翻译抑制。

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