Trypanosome alternative oxidase (TAO) is the only terminal oxidase found within the mitochondrial electron transport system in the bloodstream form (BF) of the parasite, the form that exist in the mammalian host. TAO expression is developmentally regulated in the bloodstream (BF) and procyclic forms (PF). Studies in our lab have demonstrated that TAO is regulated at the level of mRNA stability and de novo protein synthesis is required for the reduction of the mRNA pool in the PF form. In trypanosomes, gene expression is regulated post transcriptionally and the 3'- untranslated regions (UTRs) play important roles for this regulation process. TAO contains a long 3'- UTR of about 2 kilobases, and preliminary data suggest that it is most likely involved in the transcript stability in the PF. Recent evidence suggest that TAO and the cytochrome pathway protein expression are coodinately regulated, in Trypanosoma brucei. Thus, we propose here, to investigate the role of the specific regions of TAO 3'-UTR in the regulation of TAO gene expression in Trypanosoma brucei. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
1F31GM077048-01
Application #
6986845
Study Section
Special Emphasis Panel (ZRG1-IDM-P (29))
Program Officer
Gaillard, Shawn R
Project Start
2005-09-01
Project End
2007-08-31
Budget Start
2005-09-01
Budget End
2006-08-31
Support Year
1
Fiscal Year
2005
Total Cost
$33,294
Indirect Cost
Name
Meharry Medical College
Department
Microbiology/Immun/Virology
Type
Other Domestic Higher Education
DUNS #
041438185
City
Nashville
State
TN
Country
United States
Zip Code
37208