The applicant will continue his studies aimed at understanding the roles of RNA-protein interactions in functions directed by the 5'-NCR of picornavirus RNAs. Although other activities (eg. virion assembly) may be associated with the 5'-NCR of picornavirus genomic RNAs, he will focus his efforts on functions (ie. viral translation and RNA replication) known to be directed by this region of viral RNAs. For translation functions he will test the hypothesis that specific ribonucleoprotein complexes between cellular proteins and uncapped viral RNAs are required prior to binding ribosomes for initiation of cap-independent protein synthesis. For the replication functions, the PI will test the hypothesis that interaction of a cellular RNA binding protein (PCBP2) with a specific sequence in the 5'-NCR of poliovirus RNA and the viral protein 3CD is necessary for initiation of viral RNA synthesis. He will take advantage of his collection of viable mutants and pseudorevertants containing site-directed lesions in the 5'-NCR as well as a number of biochemical assays for functional associations between the 5'-NCR and cellular or viral proteins. Specifically, the PI will: (1) Elucidate the role of neuronal-cell specific factors in poliovirus translation initiation. (2) Determine the cellular expression pattern and biochemical properties of PCBP2. (3) Define the function of PCBP2 in cap-independent translation via its interaction with stem-loop IV in the IRES of poliovirus RNAs. (4) Determine the relationship between PCBP2 ribonucleoprotein complex formation with stem-loop I and viral RNA replication. The applicant states that these approaches, coupled with the analysis of mutant viral growth properties in HeLa cells and neuronal cells, should provide new insights into the mechanisms employed by the picornaviruses to insure the faithful translation and replication of viral RNAs during an infection of mammalian cells. He also indicated that, more broadly, his studies will lead to a high resolution """"""""map"""""""" of specific macromolecular interactions between RNAs and protein in the orchestration of higher order structures required for effecting functions in the cytoplasm of eukaryotic cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI026765-11
Application #
6124202
Study Section
Experimental Virology Study Section (EVR)
Program Officer
Meegan, James M
Project Start
1988-07-01
Project End
2002-11-30
Budget Start
1999-12-01
Budget End
2000-11-30
Support Year
11
Fiscal Year
2000
Total Cost
$259,872
Indirect Cost
Name
University of California Irvine
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
161202122
City
Irvine
State
CA
Country
United States
Zip Code
92697
Ullmer, Wendy; Semler, Bert L (2018) Direct and Indirect Effects on Viral Translation and RNA Replication Are Required for AUF1 Restriction of Enterovirus Infections in Human Cells. MBio 9:
Lévêque, Nicolas; Garcia, Magali; Bouin, Alexis et al. (2017) Functional Consequences of RNA 5'-Terminal Deletions on Coxsackievirus B3 RNA Replication and Ribonucleoprotein Complex Formation. J Virol 91:
Ullmer, Wendy; Semler, Bert L (2016) Diverse Strategies Used by Picornaviruses to Escape Host RNA Decay Pathways. Viruses 8:
Lévêque, Nicolas; Semler, Bert L (2015) A 21st century perspective of poliovirus replication. PLoS Pathog 11:e1004825
Flather, Dylan; Semler, Bert L (2015) Picornaviruses and nuclear functions: targeting a cellular compartment distinct from the replication site of a positive-strand RNA virus. Front Microbiol 6:594
Tsai, Becky Pinjou; Jimenez, Judith; Lim, Sharon et al. (2014) A novel Bcr-Abl-mTOR-eIF4A axis regulates IRES-mediated translation of LEF-1. Open Biol 4:140180
Chase, Amanda J; Daijogo, Sarah; Semler, Bert L (2014) Inhibition of poliovirus-induced cleavage of cellular protein PCBP2 reduces the levels of viral RNA replication. J Virol 88:3192-201
Chase, Amanda J; Semler, Bert L (2014) Differential cleavage of IRES trans-acting factors (ITAFs) in cells infected by human rhinovirus. Virology 449:35-44
Cathcart, Andrea L; Semler, Bert L (2014) Differential restriction patterns of mRNA decay factor AUF1 during picornavirus infections. J Gen Virol 95:1488-92
Langereis, Martijn A; Feng, Qian; Nelissen, Frank H T et al. (2014) Modification of picornavirus genomic RNA using 'click' chemistry shows that unlinking of the VPg peptide is dispensable for translation and replication of the incoming viral RNA. Nucleic Acids Res 42:2473-82

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