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JCCC Member Directory

Randolph E. Wall, Ph.D.
Randolph E. Wall, Ph.D.

Affiliation(s):

Professor, Department of Microbiology, Immunology, and Molecular Genetics
Member, JCCC Tumor Immunology Program Area

Contact Information:

Phone:
(310) 825-7523
E-mail:

Scientific Interest(s):

Dr. Randolph Wall's research focuses on genes and mechanisms controlling B-lymphocyte development.

The stages in B-lymphocyte development are delineated by the activation and transcription of immunoglobulin genes and other tissue-specific genes. Research in Wall's laboratory is specifically directed at discovering the molecular mechanisms which control B-cell development by the cloning of B-cell-specific genes and the characterization of their function and regulation. The best studied B-cell-specific gene identified here (B29) codes for a critical member of the antigen receptor complex on B-cells and is essential for B-cell activation and development. Transcription factors shown to control the B29 promoter are now known to regulate the appearance of the earliest committed lymphoid precursor cells. B29 expression is critical for development of the earliest B-lineage precursors (i.e., pro-B and pre-B cells). Aberrant expression of the B29 gene is implicated in human chronic lymphocytic leukemia (B-CLL).

Another area of research in the Wall lab is directed at resolving the cytokines, signaling events and transcription factors which activate and control immunoglobulin gene expression in B-cell development. This research uses the combined approaches of molecular biology, immunology and genetics.

Selected Cancer-Related Publications:

Henson SE, Tsai SC, Malone CS, Soghomonian SV, Ouyang Y, Wall R, Marahrens Y, Teitell MA. Pir51, a Rad51-interacting protein with high expression in aggressive lymphoma, controls mitomycin C sensitivity and prevents chromosomal breaks. Mutat Res. 2006; 601(1-2): 113-24.

Doerr JR, Malone CS, Fike FM, Gordon MS, Soghomonian SV, Thomas RK, Tao Q, Murray PG, Diehl V, Teitell MA, Wall R. Patterned CpG methylation of silenced B cell gene promoters in classical Hodgkin lymphoma-derived and primary effusion lymphoma cell lines. J Mol Biol. 2005; 350(4): 631-40.

Patrone L, Henson SE, Wall R, Malone CS. A conserved sequence upstream of the B29 (Ig beta, CD79b) gene interacts with YY1. Mol Biol Rep. 2004; 31(1): 1-11.

French SW, Malone CS, Shen RR, Renard M, Henson SE, Miner MD, Wall R, Teitell MA. Sp1 transactivation of the TCL1 oncogene. J Biol Chem. 2003; 278(2): 948-55.

Gordon MS, Kanegai CM, Doerr JR, Wall R. Somatic hypermutation of the B cell receptor genes B29 (Igbeta, CD79b) and mb1 (Igalpha, CD79a). Proc Natl Acad Sci U S A. 2003; 100(7): 4126-31.