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鉴定出13种新型人类修饰引导RNA。

Identification of 13 novel human modification guide RNAs.

作者信息

Vitali Patrice, Royo Hélène, Seitz Hervé, Bachellerie Jean-Pierre, Hüttenhofer Alexander, Cavaillé Jérôme

机构信息

Institute for Molecular Biology, Department of Functional Genomics, University of Innsbruck, Peter-Mayr-Strasse 4b, 6020 Innsbruck, Austria.

出版信息

Nucleic Acids Res. 2003 Nov 15;31(22):6543-51. doi: 10.1093/nar/gkg849.

DOI:10.1093/nar/gkg849
PMID:14602913
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC275545/
Abstract

Members of the two expanding RNA subclasses termed C/D and H/ACA RNAs guide the 2'-O-methylations and pseudouridylations, respectively, of rRNA and spliceosomal RNAs (snRNAs). Here, we report on the identification of 13 novel human intron-encoded small RNAs (U94-U106) belonging to the two subclasses of modification guides. Seven of them are predicted to direct 2'-O-methylations in rRNA or snRNAs, while the remainder represent novel orphan RNA modification guides. From these, U100, which is exclusively detected in Cajal bodies (CBs), is predicted to direct modification of a U6 snRNA uridine, U(9), which to date has not been found to be pseudouridylated. Hence, within CBs, U100 might function in the folding pathway or other aspects of U6 snRNA metabolism rather than acting as a pseudouridylation guide. U106 C/D snoRNA might also possess an RNA chaperone activity only since its two conserved antisense elements match two rRNA sequences devoid of methylated nucleotides and located remarkably close to each other within the 18S rRNA secondary structure. Finally, we have identified a retrogene for U99 snoRNA located within an intron of the Siat5 gene, supporting the notion that retro-transposition events might have played a substantial role in the mobility and diversification of snoRNA genes during evolution.

摘要

被称为C/D和H/ACA RNA的两个不断扩展的RNA亚类的成员,分别指导核糖体RNA(rRNA)和剪接体RNA(snRNA)的2'-O-甲基化和假尿苷酸化。在此,我们报告了13种新的人类内含子编码小RNA(U94-U106)的鉴定结果,它们属于修饰指导的两个亚类。其中7种预计可指导rRNA或snRNA中的2'-O-甲基化,其余的则代表新的孤儿RNA修饰指导分子。其中,仅在卡哈尔体(CBs)中检测到的U100,预计可指导U6 snRNA尿苷U(9)的修饰,而U(9)迄今为止尚未发现有假尿苷酸化现象。因此,在CBs内,U100可能在U6 snRNA代谢的折叠途径或其他方面发挥作用,而不是作为假尿苷酸化指导分子。U106 C/D小核仁RNA(snoRNA)可能也仅具有RNA伴侣活性,因为其两个保守的反义元件与两个没有甲基化核苷酸的rRNA序列匹配,并且在18S rRNA二级结构中彼此非常接近。最后,我们在Siat5基因的一个内含子中鉴定出了U99 snoRNA的一个反转录基因,这支持了反转录事件可能在进化过程中snoRNA基因的移动性和多样性方面发挥了重要作用这一观点。

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本文引用的文献

1
A common sequence motif determines the Cajal body-specific localization of box H/ACA scaRNAs.一个共同的序列基序决定了盒式H/ACA scaRNA在卡哈尔体中的特异性定位。
EMBO J. 2003 Aug 15;22(16):4283-93. doi: 10.1093/emboj/cdg394.
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RNomics in Drosophila melanogaster: identification of 66 candidates for novel non-messenger RNAs.黑腹果蝇中的RNA组学:66种新型非信使RNA候选物的鉴定。
Nucleic Acids Res. 2003 May 15;31(10):2495-507. doi: 10.1093/nar/gkg361.
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Modification of Sm small nuclear RNAs occurs in the nucleoplasmic Cajal body following import from the cytoplasm.Sm小核RNA的修饰在从细胞质输入后于核质中的卡哈尔体中发生。
EMBO J. 2003 Apr 15;22(8):1878-88. doi: 10.1093/emboj/cdg187.
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Targeting of U4/U6 small nuclear RNP assembly factor SART3/p110 to Cajal bodies.U4/U6小核核糖核蛋白组装因子SART3/p110定位于卡哈尔体。
J Cell Biol. 2003 Feb 17;160(4):505-16. doi: 10.1083/jcb.200210087. Epub 2003 Feb 10.
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Experimental RNomics: identification of 140 candidates for small non-messenger RNAs in the plant Arabidopsis thaliana.实验性RNA组学:拟南芥中小非信使RNA的140个候选物的鉴定。
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Cloning and comparative sequence analysis of PUM1 and PUM2 genes, human members of the Pumilio family of RNA-binding proteins.RNA 结合蛋白 Pumilio 家族的人类成员 PUM1 和 PUM2 基因的克隆及比较序列分析
Gene. 2002 Oct 16;299(1-2):195-204. doi: 10.1016/s0378-1119(02)01060-0.
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The expanding snoRNA world.不断扩展的小核仁RNA世界
Biochimie. 2002 Aug;84(8):775-90. doi: 10.1016/s0300-9084(02)01402-5.
9
A Cajal body-specific pseudouridylation guide RNA is composed of two box H/ACA snoRNA-like domains.一种Cajal体特异性假尿苷化向导RNA由两个盒式H/ACA小核仁RNA样结构域组成。
Nucleic Acids Res. 2002 Nov 1;30(21):4643-9. doi: 10.1093/nar/gkf592.
10
Identification of tandemly-repeated C/D snoRNA genes at the imprinted human 14q32 domain reminiscent of those at the Prader-Willi/Angelman syndrome region.在印记的人类14q32区域鉴定串联重复的C/D小核仁RNA基因,这让人联想到普拉德-威利/安吉尔曼综合征区域的那些基因。
Hum Mol Genet. 2002 Jun 15;11(13):1527-38. doi: 10.1093/hmg/11.13.1527.