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Domains of Human U4atac SnRNA Required for U12-dependent Splicing in Vivo

Overview
Specialty Biochemistry
Date 2002 Nov 1
PMID 12409455
Citations 17
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Abstract

U4atac snRNA forms a base-paired complex with U6atac snRNA. Both snRNAs are required for the splicing of the minor U12-dependent class of eukaryotic nuclear introns. We have developed a new genetic suppression assay to investigate the in vivo roles of several regions of U4atac snRNA in U12-dependent splicing. We show that both the stem I and stem II regions, which have been proposed to pair with U6atac snRNA, are required for in vivo splicing. Splicing activity also requires U4atac sequences in the 5' stem-loop element that bind a 15.5 kDa protein that also binds to a similar region of U4 snRNA. In contrast, mutations in the region immediately following the stem I interaction region, as well as a deletion of the distal portion of the 3' stem-loop element, were active for splicing. Complete deletion of the 3' stem-loop element abolished in vivo splicing function as did a mutation of the Sm protein binding site. These results show that the in vivo sequence requirements of U4atac snRNA are similar to those described previously for U4 snRNA using in vitro assays and provide experimental support for models of the U4atac/U6atac snRNA interaction.

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References
1.
Wersig C, Bindereif A . Conserved domains of human U4 snRNA required for snRNP and spliceosome assembly. Nucleic Acids Res. 1990; 18(21):6223-9. PMC: 332485. DOI: 10.1093/nar/18.21.6223. View

2.
Bordonne R, Banroques J, Abelson J, Guthrie C . Domains of yeast U4 spliceosomal RNA required for PRP4 protein binding, snRNP-snRNP interactions, and pre-mRNA splicing in vivo. Genes Dev. 1990; 4(7):1185-96. DOI: 10.1101/gad.4.7.1185. View

3.
Vankan P, McGuigan C, Mattaj I . Roles of U4 and U6 snRNAs in the assembly of splicing complexes. EMBO J. 1992; 11(1):335-43. PMC: 556454. DOI: 10.1002/j.1460-2075.1992.tb05056.x. View

4.
Wersig C, Bindereif A . Reconstitution of functional mammalian U4 small nuclear ribonucleoprotein: Sm protein binding is not essential for splicing in vitro. Mol Cell Biol. 1992; 12(4):1460-8. PMC: 369587. DOI: 10.1128/mcb.12.4.1460-1468.1992. View

5.
Dandekar T, Tollervey D . Mutational analysis of Schizosaccharomyces pombe U4 snRNA by plasmid exchange. Yeast. 1992; 8(8):647-53. DOI: 10.1002/yea.320080808. View