The focus of this renewal application is the structure and function of aI2, a self-splicing intron from yeast mitochondria. In previous work it was shown that the ORF 1) is a maturase, 2) is a site- specific mobile element, and 3) contains homology to reverse transcriptases (RT), DNA endonucleases (Zn), and retroviral proteases (P). There are three major specific aims. 1) The aI2 intron is expressed as a 96kD precursor, and processed to p62 which contains RT, X and Zn. The applicant will determine if p62 also contains P and Z, a domain found in some non-LTR retroelements, and whether these sequences are important for splicing and/or mobility. 2) To determine the role of the maturase in splicing, two approaches are proposed. First, the PI will test the specific hypothesis that p62 promotes proper folding of the intron by looking for RNA-protein interactions using a variety of standard techniques. Associations with other proteins will also be assayed using the knowledge that p62 sediments as several RNPs. These biochemical approaches will be supplemented with information obtained from the creation of aI mutants and suppressors. Second, he will attempt to develop a p62-dependent splicing system, based on the fact that aI does not self-splice at low salt in vitro. Both forward and reverse splicing assays are described. 3) A working model for group II intron mobility will be tested which involves reverse transcription of the aI2- containing pre-mRNA and site-specific insertion into recipient, intronless genes. In addition to RT, Zn is essential, perhaps by providing the primer for first-strand cDNA synthesis. The presumptive case for an RNA intermediate will be definitively tested a la Boeke and Fink. The relationship of splicing to mobility will be investigated by the analysis of mutants, including the possibility that the excised intron is involved. The role of exon sequences in recipient and donor will be distinguished and the in vivo mobility requirements will be compared to those for a new in vitro endonuclease assay (to be carried by the Lambowitz laboratory). Finally, the applicant will investigate unusual mobility events which may involve an RT-independent pathway and a reverse-splicing-dependent pathway.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM031480-15
Application #
2021934
Study Section
Molecular Biology Study Section (MBY)
Project Start
1990-08-01
Project End
1999-11-30
Budget Start
1996-12-01
Budget End
1997-11-30
Support Year
15
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Biochemistry
Type
Schools of Medicine
DUNS #
City
Dallas
State
TX
Country
United States
Zip Code
75390
Huang, Hon-Ren; Rowe, Claire E; Mohr, Sabine et al. (2005) The splicing of yeast mitochondrial group I and group II introns requires a DEAD-box protein with RNA chaperone function. Proc Natl Acad Sci U S A 102:163-8
Dickson, Lorna; Connell, Stuart; Huang, Hon-Ren et al. (2004) Abortive transposition by a group II intron in yeast mitochondria. Genetics 168:77-87
Schafer, Bernd; Gan, Lin; Perlman, Philip S (2003) Reverse transcriptase and reverse splicing activities encoded by the mobile group II intron cobI1 of fission yeast mitochondrial DNA. J Mol Biol 329:191-206
Huang, Hon-Ren; Chao, Michael Y; Armstrong, Barbara et al. (2003) The DIVa maturase binding site in the yeast group II intron aI2 is essential for intron homing but not for in vivo splicing. Mol Cell Biol 23:8809-19
Podar, Mircea; Mullineaux, Lauren; Huang, Hon-Ren et al. (2002) Bacterial group II introns in a deep-sea hydrothermal vent environment. Appl Environ Microbiol 68:6392-8
Dickson, L; Huang, H R; Liu, L et al. (2001) Retrotransposition of a yeast group II intron occurs by reverse splicing directly into ectopic DNA sites. Proc Natl Acad Sci U S A 98:13207-12
Chu, V T; Adamidi, C; Liu, Q et al. (2001) Control of branch-site choice by a group II intron. EMBO J 20:6866-76
Zhang, Y; Bell, A; Perlman, P S et al. (2000) Pentamidine inhibits mitochondrial intron splicing and translation in Saccharomyces cerevisiae. RNA 6:937-51
Eskes, R; Liu, L; Ma, H et al. (2000) Multiple homing pathways used by yeast mitochondrial group II introns. Mol Cell Biol 20:8432-46
Podar, M; Perlman, P S (1999) Photocrosslinking of 4-thio uracil-containing RNAs supports a side-by-side arrangement of domains 5 and 6 of a group II intron. RNA 5:318-29

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