Studies from this laboratory and others from the last five years indicate that rhree distinct proteins are required specifically to bind mRNA to 43S preinitiation complexes and these three proteins are eukaryotic initiation factor (eIF) 4A, 4B and 4F. In the most general terms, eIF-4F recognizes the 5' m7G cap structure of eukaryotic mKNAs, eIF-4A is an ATP-dependent, single-stranded RNA binding protein, and eIF-4B coordinates their interaction. Our current efforts are designed to examine how these three factors (and perhaps others) are involved in the following: 1) How do 4OS subunits bind to mRNAs and move the mRNA to the initiating AUG codon? 2) Is the general mechanism for reinitiation (the downstream initiation of a bicistronic mRNA) the same as for the first initiation event or is it dissimilar? 3) Does internal initiation occur in polycistronic mRNAs (usually viral) and if so, by what mechanism? To examine these questions, we intend to use purified factors in both a fractionated system and a nuclease treated lysate and with SP6 transcripts to yield a series of """"""""mutated"""""""" mRNAs. These studies will extend our current knowledge as well as confirm previous notions on the function of the three mRNA specific initiation factors. In particular, these studies should offer unique insights into the initiation of uncapped mRNAs and polycistronic mRNAs, both usually only found in virally infected cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM026796-11
Application #
3274249
Study Section
Physiological Chemistry Study Section (PC)
Project Start
1979-07-01
Project End
1993-07-31
Budget Start
1990-08-01
Budget End
1991-07-31
Support Year
11
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Case Western Reserve University
Department
Type
Schools of Medicine
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106
Kaye, Nicholas M; Emmett, Kelly J; Merrick, William C et al. (2009) Intrinsic RNA binding by the eukaryotic initiation factor 4F depends on a minimal RNA length but not on the m7G cap. J Biol Chem 284:17742-50
Svitkin, Yuri V; Evdokimova, Valentina M; Brasey, Ann et al. (2009) General RNA-binding proteins have a function in poly(A)-binding protein-dependent translation. EMBO J 28:58-68
Pisarev, Andrey V; Kolupaeva, Victoria G; Pisareva, Vera P et al. (2006) Specific functional interactions of nucleotides at key -3 and +4 positions flanking the initiation codon with components of the mammalian 48S translation initiation complex. Genes Dev 20:624-36
Robert, Francis; Gao, Hong Qing; Donia, Marwa et al. (2006) Chlorolissoclimides: new inhibitors of eukaryotic protein synthesis. RNA 12:717-25
Robert, Francis; Kapp, Lee D; Khan, Shakila N et al. (2006) Initiation of protein synthesis by hepatitis C virus is refractory to reduced eIF2.GTP.Met-tRNA(i)(Met) ternary complex availability. Mol Biol Cell 17:4632-44
Hui, Daniel J; Terenzi, Fulvia; Merrick, William C et al. (2005) Mouse p56 blocks a distinct function of eukaryotic initiation factor 3 in translation initiation. J Biol Chem 280:3433-40
Honda, Kazuhiro; Smith, Mark A; Zhu, Xiongwei et al. (2005) Ribosomal RNA in Alzheimer disease is oxidized by bound redox-active iron. J Biol Chem 280:20978-86
Komar, Anton A; Gross, Stephane R; Barth-Baus, Diane et al. (2005) Novel characteristics of the biological properties of the yeast Saccharomyces cerevisiae eukaryotic initiation factor 2A. J Biol Chem 280:15601-11
Orton, Kevin C; Ling, Jun; Waskiewicz, Andrew J et al. (2004) Phosphorylation of Mnk1 by caspase-activated Pak2/gamma-PAK inhibits phosphorylation and interaction of eIF4G with Mnk. J Biol Chem 279:38649-57
Merrick, William C (2004) Cap-dependent and cap-independent translation in eukaryotic systems. Gene 332:1-11

Showing the most recent 10 out of 73 publications