Human cytomegalovirus (HCMV) is a widespread pathogen of growing medical importance HCMV is an opportunistic pathogen in AIDS patients, transplant recipients and is also the leading cause of virally induced birth defects Based on the significant threats posed by HCMV, the overall goal of this research is to provide a more complete understanding of HCMV replication More specifically, the proposed research will explore the hypothesis that a 5kb immediate early transcript functions in the capacity of an RNA molecule Two research aims are outlined in this proposal (1) characterize the synthesis, structure and localization of the 5kb transcript and (2) further explore the function of transcripts derived from the 5kb region by constructing a viral mutant Detailed characterization of the function of the 5kb transcript will provide the opportunity to understand HCMV replication as well as illuminate aspects of cellular biology and possible allow development of therapeutic interventions for HCMV infection.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32AI054034-03
Application #
6896367
Study Section
Special Emphasis Panel (ZRG1-F08 (20))
Program Officer
Beisel, Christopher E
Project Start
2003-05-01
Project End
2006-04-30
Budget Start
2005-05-01
Budget End
2006-04-30
Support Year
3
Fiscal Year
2005
Total Cost
$51,548
Indirect Cost
Name
Princeton University
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
002484665
City
Princeton
State
NJ
Country
United States
Zip Code
08544
Kulesza, Caroline A; Shenk, Thomas (2006) Murine cytomegalovirus encodes a stable intron that facilitates persistent replication in the mouse. Proc Natl Acad Sci U S A 103:18302-7
Kulesza, Caroline A; Shenk, Thomas (2004) Human cytomegalovirus 5-kilobase immediate-early RNA is a stable intron. J Virol 78:13182-9