Abstract

U2 RNA is one of five small nuclear RNAs that participate in the majority of mRNA splicing. In addition to its role in mRNA splicing, the biosynthesis of U2 RNA and three of the other spliceosomal RNAs is itself an intriguing process involving nuclear export followed by 5'-cap hypermethylation, assembly with specific proteins, 3' end processing, and then nuclear import. Previous work has identified sequences near the 3' end of pre-U2 RNA that are required for accurate and efficient processing. In this study, we have investigated the structural basis of U2 RNA 3' end processing by chemical and enzymatic probing methods. Our results demonstrate that the 3' end of pre-U2 RNA is a minihelix with an estimated stabilization free energy of -6.9 kcal/mol. Parallel RNA structure mapping experiments with mutant pre-U2 RNAs revealed that the presence of this 3' minihelix is itself not required for in vitro 3'-processing of pre-U2 RNA, in support of earlier studies implicating internal regions of pre-U2 RNA. Other considerations raise the possibility that this distinctive structural motif at the 3' end of pre-U2 RNA plays a role in the cleavage of the precursor from its longer primary transcript or in its nucleocytoplasmic traffic.

Highlights

  • The major spliceosome that operates on most eukaryotic pre-mRNAs contains five small RNAs, U1, U2, U4, U5, and U6

  • The other four major spliceosomal RNAs, U1, U2, U4, and U5, are transcribed by RNA polymerase II in mammalian cells as precursor molecules extended at their 3Ј ends that are exported to the cytoplasm where they undergo cap hypermethylation and ribonucleoprotein assembly followed by 3Ј end processing and nuclear import (4 –13)

  • The mammalian precursor molecules of U1, U2, U4, and U5 RNAs have been defined in several studies (4, 6, 8 –11, 14), and their 3Ј-processing has been well characterized for U2 RNA [11, 13, 15,16,17]

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Summary

Introduction

The major spliceosome that operates on most eukaryotic pre-mRNAs contains five small RNAs, U1, U2, U4, U5, and U6. We have investigated the structural basis of U2 RNA 3؅ end processing by chemical and enzymatic probing methods.

Results
Conclusion
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