Organisms develop in precisely organized patterns that are controlled by complex cellular mechanisms. Many of these mechanisms are conserved throughout higher eukaryotes. Some proteins are responsible for directing the development of specific parts of the body (e.g. homeotic proteins). Others, such as RNA helicase A (RHA), are involved in basic cellular processes in all cells, and defects in these proteins produce developmental abnormalities throughout the organism. RNA helicases are involved in various steps of mRNA metabolism, such as transcription and splicing. Helicases use energy from A1'P hydrolysis to separate duplex nucleic acids into single strands. RNA helicase A is essential for proper development in mice, flies, and the model organism C. elegans. Its precise cellular function is unknown, but in vitro experiments with the human RHA homolog provide some clues. For example, human RHA is required for the in vitro transcription activation of RNA polymerase II by CBP, a protein involved in cAMP signaling in the cell. Mutations in CBP cause the human disease Rubinstein-Taybi syndrome, which is associated with developmental abnormalities such as broad digits and mental retardation. Human RHA is also responsible for genomic viral RNA export from the nucleus. In order to determine the precise cellular function of RHA, this proposal involves biochemical and genetic studies of RHA- 1, the RHA homolog in C. elegans. RNA binding, ATPase, and RNA helicase properties of RHA-1 will be studied in vitro using purified protein and well-defined RNA substrates. Candidate proteins that may bind to RHA- 1 in the cell will be tested using the yeast two-hybrid system. These binding partners may reveal the cellular function of RHA-1 and they may alter the biochemical activity of RHA- 1. Finally, worms with reduced function of RHA- 1 and/or its binding partners will be generated to determine the physiological function of RHA-1. The ultimate goal is to determine the cellular function of RHA-1 to obtain a better understanding of how transcription and mRNA processing affect the development in all eukaryotes, including humans.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
1R15GM061520-01A1
Application #
6357654
Study Section
Genetics Study Section (GEN)
Program Officer
Rhoades, Marcus M
Project Start
2001-08-01
Project End
2003-12-31
Budget Start
2001-08-01
Budget End
2003-12-31
Support Year
1
Fiscal Year
2001
Total Cost
$145,000
Indirect Cost
Name
University of South Florida
Department
Type
Schools of Arts and Sciences
DUNS #
City
Tampa
State
FL
Country
United States
Zip Code
33612
Walstrom, Katherine M; Schmidt, Deborah; Bean, Christopher J et al. (2005) RNA helicase A is important for germline transcriptional control, proliferation, and meiosis in C. elegans. Mech Dev 122:707-20