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Using an in vitro system we have recently shown that the 3' ends of human pre-snRNAs synthesized by RNA polymerase II are produced by RNA processing directed by the snRNA gene-specific 3' box. Towards a complete characterization of this processing reaction we have further investigated the in vitro requirements for proper 3' end formation of pre-U1 snRNA. Here we show that the 5' cap plays a stimulatory role and processing requires creatine phosphate. Our results also indicate that the pre-U1 processing activity is heat sensitive and that an RNA component is required. In addition, the exact sequence adjacent to the 3' box influences the position of the pre-U1 3' end produced in vitro. Interestingly, the processing extract active for 3'-box-dependent processing also contains an activity that converts the 3' end of RNA containing the U1 Sm protein binding site and the 3' terminal stem-loop into the mature form.

Original publication

DOI

10.1093/nar/gkh619

Type

Journal article

Journal

Nucleic Acids Res

Publication Date

2004

Volume

32

Pages

2987 - 2994

Keywords

Adenosine Triphosphate, Base Sequence, Binding Sites, Coenzymes, Enzyme Stability, HeLa Cells, Hot Temperature, Humans, Molecular Sequence Data, Nucleic Acid Conformation, Phosphocreatine, RNA Caps, RNA Processing, Post-Transcriptional, RNA, Small Nuclear, Ribonucleoproteins