4.5 Article

The transcription factor, Bright, is not expressed in all human B lymphocyte subpopulations

Journal

CELLULAR IMMUNOLOGY
Volume 228, Issue 1, Pages 42-53

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.cellimm.2004.03.004

Keywords

bright; B cell; BTK; XLA

Funding

  1. NIAID NIH HHS [T32 AI007633, AI45864] Funding Source: Medline
  2. PHS HHS [07633, 44215] Funding Source: Medline

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Bright is an ARID family transcription factor that increases immunoglobulin heavy chain transcription. In the mouse, Bright expression is tightly regulated and B cell-restricted and the Bright protein associates with Bruton's tyrosine kinase (Btk), the defective enzyme in X-linked immunodeficiency. Human X-linked agammaglobulinemia results from defects in Btk and leads to early blocks in B lymphocyte development. Because so little is known about human Bright, we sought to determine where human Bright is expressed in normal B cell differentiation and whether it also forms complexes with Btk. Although human and mouse Bright exhibited similar expression patterns in normal B cells, many human transformed B cell lines did not express Bright protein. However, the human protein bound prototypic Bright DNA-binding motifs and, like mouse Bright, was capable of associating with Btk. These data suggest potentially important similarities exist in Bright expression and activity in human and mouse B lymphocytes. (C) 2004 Elsevier Inc. All rights reserved.

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