Richard Patricia, Darzacq Xavier, Bertrand Edouard, Jády Beáta E, Verheggen Céline, Kiss Tamás
Laboratoire de Biologie Moléculaire Eucaryote du CNRS, UMR5099, IFR109, 118 route de Narbonne, 31062 Toulouse, France.
EMBO J. 2003 Aug 15;22(16):4283-93. doi: 10.1093/emboj/cdg394.
Post-transcriptional synthesis of 2'-O-methylated nucleotides and pseudouridines in Sm spliceosomal small nuclear RNAs takes place in the nucleoplasmic Cajal bodies and it is directed by guide RNAs (scaRNAs) that are structurally and functionally indistinguishable from small nucleolar RNAs (snoRNAs) directing rRNA modification in the nucleolus. The scaRNAs are synthesized in the nucleoplasm and specifically targeted to Cajal bodies. Here, mutational analysis of the human U85 box C/D-H/ACA scaRNA, followed by in situ localization, demonstrates that box H/ACA scaRNAs share a common Cajal body-specific localization signal, the CAB box. Two copies of the evolutionarily conserved CAB consensus (UGAG) are located in the terminal loops of the 5' and 3' hairpins of the box H/ACA domains of mammalian, Drosophila and plant scaRNAs. Upon alteration of the CAB boxes, mutant scaRNAs accumulate in the nucleolus. In turn, authentic snoRNAs can be targeted into Cajal bodies by addition of exogenous CAB box motifs. Our results indicate that scaRNAs represent an ancient group of small nuclear RNAs which are localized to Cajal bodies by an evolutionarily conserved mechanism.
Sm剪接体小核RNA中2'-O-甲基化核苷酸和假尿苷的转录后合成发生在核质中的卡哈尔体中,由指导RNA(scaRNA)指导,scaRNA在结构和功能上与指导核仁中rRNA修饰的小核仁RNA(snoRNA)没有区别。scaRNA在核质中合成,并特异性定位于卡哈尔体。在这里,对人类U85盒C/D-H/ACA scaRNA进行突变分析,然后进行原位定位,结果表明盒H/ACA scaRNA共享一个共同的卡哈尔体特异性定位信号,即CAB盒。进化保守的CAB共有序列(UGAG)的两个拷贝位于哺乳动物、果蝇和植物scaRNA盒H/ACA结构域5'和3'发夹的末端环中。改变CAB盒后,突变的scaRNA在核仁中积累。反过来,通过添加外源性CAB盒基序,可以将真正的snoRNA靶向到卡哈尔体中。我们的结果表明,scaRNA代表了一组古老的小核RNA,它们通过一种进化保守的机制定位于卡哈尔体。