Sturchler C, Carbon P, Krol A
Institut de Biologie Moléculaire et Cellulaire du CNRS, Strasbourg, France.
Nucleic Acids Res. 1992 Mar 25;20(6):1215-21. doi: 10.1093/nar/20.6.1215.
We present evidence for the existence of an additional long-range interaction in vertebrate U1 snRNAs. By submitting human U1 snRNP, HeLa nuclear extracts, authentic human or X. laevis in vitro transcribed U1 snRNAs to RNase V1, a nuclease specific for double-stranded regions, cleavages occurred in the sequence psi psi ACC (positions 5-9) residing in the 5' terminal region of the RNA. The RNase V1 sensitive region is insensitive to single-stranded probes, something unexpected knowing that it was considered single-stranded in order to base-pair to pre-mRNA 5' splice site. We have identified the sequence GGUAG (positions 132-136) as the only possible 3' partner. Mutants, either abolishing or restoring the interaction between the partners, coupled to an RNase V1 assay, served to substantiate this base-pairing model. The presence of this additional helix, even detected in nuclear extracts under in vitro splicing conditions, implies that a conformational change must occur to release a free U1 snRNA 5' end.
我们提供了脊椎动物U1小核RNA(snRNA)中存在额外长程相互作用的证据。通过将人U1小核核糖核蛋白颗粒(snRNP)、HeLa细胞核提取物、真实的人或非洲爪蟾体外转录的U1 snRNA用RNase V1(一种对双链区域特异的核酸酶)处理,在RNA 5'末端区域的ψψACC序列(第5 - 9位)出现了切割。RNase V1敏感区域对单链探针不敏感,考虑到它为了与前体mRNA的5'剪接位点碱基配对而被认为是单链,这是出乎意料的。我们已确定序列GGUAG(第132 - 136位)是唯一可能的3'配对序列。与RNase V1分析相结合的、消除或恢复配对序列间相互作用的突变体,用于证实这种碱基配对模型。这种额外螺旋结构的存在,甚至在体外剪接条件下的细胞核提取物中也能检测到,这意味着必须发生构象变化以释放游离的U1 snRNA 5'末端。