Ul small nuclear RNAs (Ul RNAs) are abundant RNA molecules which, in the form of Ul-ribonucleoprotein particles (Ul snRNPs) are found in the nuclei of all higher eukaryotes; they are generally thought to be essential for the process of pre-mRNA splicing. The long-range goals of this project are to define the structures required for Ul RNA synthesis and function, and to elucidate how differential accumulation of Ul RNAs influences overall gene expression. The work will be carried out in three different organisms, human, frog and mouse, in order to utilize particular advantages of each system. The structural features of Ul DNA templates and Ul RNAs will be probed by introduction of wild-type or mutated Ul RNA genes into transcription systems either by microinjection or by transfection. Sequences upstream, downstream, and within the coding regions of cloned human and X. laevis Ul RNA genes will be analyzed for their function in transcription and roles in formation of mature Ul snRNPs. The newly synthesized Ul RNAs and/or Ul snRNPs will be characterized with respect to 5' and 3' maturation, base modification, association with snRNP proteins, and their ability to participate in the splicing of pre-mRNAs. Assays for participation of specific Ul RNAs in pre-mRNA splicing will be developed and applied to the analysis of how Ul RNA functions. The developmental control of Ul RNA gene expression will be studied in both frog and mouse embryos and tissues. The stages at which U1 gene expression changes from the embryonic to the somatic pattern will be determined and the mechanisms of control will be investigated. The ability of the different types of Ul RNAs to support the splicing of a variety of pre-mRNAs will be tested, as well as the ability of these RNAs to bind the normal complement of snRNP-associated proteins.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM030220-06
Application #
3277861
Study Section
Molecular Biology Study Section (MBY)
Project Start
1982-04-01
Project End
1988-11-30
Budget Start
1987-04-01
Budget End
1988-11-30
Support Year
6
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Lund, Elsebet; Liu, Mingzhu; Hartley, Rebecca S et al. (2009) Deadenylation of maternal mRNAs mediated by miR-427 in Xenopus laevis embryos. RNA 15:2351-63
Eis, Peggy S; Garcia-Blanco, Mariano A (2008) Quantification of microRNAs, splicing isoforms, and homologous mRNAs with the invader assay. Methods Mol Biol 488:279-318
Lund, E; Dahlberg, J E (2006) Substrate selectivity of exportin 5 and Dicer in the biogenesis of microRNAs. Cold Spring Harb Symp Quant Biol 71:59-66
Eis, Peggy S; Tam, Wayne; Sun, Liping et al. (2005) Accumulation of miR-155 and BIC RNA in human B cell lymphomas. Proc Natl Acad Sci U S A 102:3627-32
Lund, Elsebet; Guttinger, Stephan; Calado, Angelo et al. (2004) Nuclear export of microRNA precursors. Science 303:95-8
Trotta, Christopher R; Lund, Elsebet; Kahan, Lawrence et al. (2003) Coordinated nuclear export of 60S ribosomal subunits and NMD3 in vertebrates. EMBO J 22:2841-51
Dahlberg, James E; Lund, Elsebet; Goodwin, Elizabeth B (2003) Nuclear translation: what is the evidence? RNA 9:1-8
Glodowski, Doreen R; Petersen, Jeannine M; Dahlberg, James E (2002) Complex nuclear localization signals in the matrix protein of vesicular stomatitis virus. J Biol Chem 277:46864-70
Johnson, Arlen W; Lund, Elsebet; Dahlberg, James (2002) Nuclear export of ribosomal subunits. Trends Biochem Sci 27:580-5
Rutjes, S A; Lund, E; van der Heijden, A et al. (2001) Identification of a novel cis-acting RNA element involved in nuclear export of hY RNAs. RNA 7:741-52

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