The importance of E2A proteins as potent regulators of B- and T- cell formation is firmly established, but their role in activated B- or plasma cells remains unclear. We have recently amplified the cDNA encoding a B-cell restricted basic helix-loop-helix transcription factor member, designated activated B-cell factor 1, from a cDNA library prepared from human plasma cells. The expression pattern of ABF-1 has been demonstrated to be restricted to activated B-cells and EBV-transformed B cell lines. The proposed studies are aimed at investigating the cell- restricted regulatory elements that govern human ABF-1 gene expression as well as analyzing the genomic organization of ABF- 1. A broad spectrum of genetic and biochemical techniques will be used, including gene cloning and sequencing, DNA transfections, electrophoretic-mobility shift assays, Western- and Southern blotting and fluorescence microscopy. The results of these studies will identify transcription factors that regulate ABF-1 gene expression in activated B lymphocytes and EBV-infected B cells. In addition, they will provide important structural information regarding ABF-1 as well as map the chromosomal location of the ABF-1 gene.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
1R15AI045767-01A1
Application #
6082787
Study Section
Cell Development and Function Integrated Review Group (CDF)
Program Officer
Prograis, Lawrence J
Project Start
2000-07-01
Project End
2003-06-30
Budget Start
2000-07-01
Budget End
2003-06-30
Support Year
1
Fiscal Year
2000
Total Cost
$87,501
Indirect Cost
Name
University of the Pacific-Stockton
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
City
Stockton
State
CA
Country
United States
Zip Code
95211