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启动子结合的全长内含子环状RNA- RNA聚合酶II复合物调节人类寄生虫中的基因表达

Promoter-Bound Full-Length Intronic Circular RNAs-RNA Polymerase II Complexes Regulate Gene Expression in the Human Parasite .

作者信息

García-Lerena Jesús Alberto, González-Blanco Gretter, Saucedo-Cárdenas Odila, Valdés Jesús

机构信息

Departamento de Bioquímica, CINVESTAV-México, Av. IPN 2508 Colonia San Pedro Zacatenco, Mexico City 07360, Mexico.

Departamento de Histología, Facultad de Medicina, Universidad Autónoma de Nuevo León, Monterrey 67700, Mexico.

出版信息

Noncoding RNA. 2022 Jan 27;8(1):12. doi: 10.3390/ncrna8010012.

Abstract

Ubiquitous eukaryotic non-coding circular RNAs are involved in numerous co- and post-transcriptional regulatory mechanisms. Recently, we reported full-length intronic circular RNAs (flicRNAs) in , with 3'ss-5'ss ligation points and 5'ss GU-rich elements essential for their biogenesis and their suggested role in transcription regulation. Here, we explored how flicRNAs impact gene expression regulation. Using CLIP assays, followed by qRT-PCR, we identified that the RabX13 control flicRNA and virulence-associated flicRNAs were bound to the HA-tagged RNA Pol II C-terminus domain in transformants. The U2 snRNA was also present in such complexes, indicating that they belonged to transcription initiation/elongation complexes. Correspondingly, inhibition of the second step of splicing using boric acid reduced flicRNA formation and modified the expression of their parental genes and non-related genes. flicRNAs were also recovered from chromatin immunoprecipitation eluates, indicating that the flicRNA-Pol II complex was formed in the promoter of their cognate genes. Finally, two flicRNAs were found to be cytosolic, whose functions remain to be uncovered. Here, we provide novel evidence of the role of flicRNAs in gene expression regulation in cis, apparently in a widespread fashion, as an element bound to the RNA polymerase II transcription initiation complex, in .

摘要

普遍存在的真核生物非编码环状RNA参与了众多的共转录和转录后调控机制。最近,我们报道了[具体物种]中的全长内含子环状RNA(flicRNAs),其3'ss-5'ss连接点和富含5'ss GU的元件对其生物合成至关重要,并且它们在转录调控中具有潜在作用。在此,我们探究了flicRNAs如何影响基因表达调控。通过CLIP分析,随后进行qRT-PCR,我们发现在[具体物种]转化体中,RabX13调控flicRNA和毒力相关flicRNA与HA标签的RNA聚合酶II C末端结构域结合。U2 snRNA也存在于此类复合物中,表明它们属于转录起始/延伸复合物。相应地,使用硼酸抑制剪接的第二步会减少flicRNA的形成,并改变其亲本基因和非相关基因的表达。flicRNAs也从染色质免疫沉淀洗脱物中回收,表明flicRNA-聚合酶II复合物在其同源基因的启动子中形成。最后,发现两种flicRNAs存在于细胞质中,其功能尚待揭示。在此,我们提供了新的证据,证明flicRNAs在[具体物种]中以一种广泛的方式顺式调控基因表达,作为与RNA聚合酶II转录起始复合物结合的元件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/246d/8876499/e16d748060ac/ncrna-08-00012-g001.jpg

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