DNA rearrangement, somatic mutation, and expression of immunoglobulin heavy chain (IgH) genes occur exclusively in B cells. During the last several years, my laboratory has identified and characterized cis and trans elements that are candidate regulators of VDJ joining, class switching and IgH gene expression. These include identification of a key B cell transcription factor, BSAP, and characterization of the IgH 3' regulatory region, which contains four enhancers. Only the most distal enhancer, hs4, appears to be active throughout B cell differentiation, as assessed in cultured cell lines. We have actively studied the extended 3' IgH region for its role in IgH gene replication, together with Roy Riblet and Carl Schildkraut. We find dramatic differences in usage of origins of DNA replication for the IgH gene cluster in cultured non-B cell lines and in B cell lines representing different stages of maturation. Changes in enhancer activation and origin usage are occurring within a single approximately 100 kb DNA segment. The hypothesis of this proposal is that in vivo, there is a temporal and developmental relationship between regulation of IgH 3' enhancers and usage of IgH origins of replication that involves a mechanistic interface. Our first goal is to determine the temporal and cell-type specific activity of hs4 as a transcriptional enhancer in vivo. We will generate mice with an hs4-regulated transgene linked to a GFP expression reporter. Mutational analysis of hs4 transcriptional activity will be carried out in cell lines. Our second goal is to locate and identify IgH origins of replication in non-B, B and plasma cell lines and to determine whether normal cells show similar utilization of specific IgH replication origins. A third goal is to determine whether a boundary for the IgH locus/ chromosomal domain is located at hs4, at the dominant downstream ori used in MEL, or in between. We will assess the chromatin configuration of the 100 kb region in which changes in enhancer activation and origin usage are both occurring.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
2R01AI013509-24A2
Application #
6195637
Study Section
Allergy and Immunology Study Section (ALY)
Program Officer
Ridge, John P
Project Start
1976-06-30
Project End
2003-06-30
Budget Start
2000-07-01
Budget End
2001-06-30
Support Year
24
Fiscal Year
2000
Total Cost
$414,705
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
009095365
City
Bronx
State
NY
Country
United States
Zip Code
10461
Birshtein, Barbara K (2014) Epigenetic Regulation of Individual Modules of the immunoglobulin heavy chain locus 3' Regulatory Region. Front Immunol 5:163
Volpi, Sabrina A; Verma-Gaur, Jiyoti; Hassan, Rabih et al. (2012) Germline deletion of Igh 3' regulatory region elements hs 5, 6, 7 (hs5-7) affects B cell-specific regulation, rearrangement, and insulation of the Igh locus. J Immunol 188:2556-66
Frezza, Domenico; Tolusso, Barbara; Giambra, Vincenzo et al. (2012) Polymorphisms of the IgH enhancer HS1.2 and risk of systemic lupus erythematosus. Ann Rheum Dis 71:1309-15
Birshtein, Barbara K (2012) The role of CTCF binding sites in the 3' immunoglobulin heavy chain regulatory region. Front Genet 3:251
Ju, Zhongliang; Chatterjee, Sanjukta; Birshtein, Barbara K (2011) Interaction between the immunoglobulin heavy chain 3' regulatory region and the IgH transcription unit during B cell differentiation. Mol Immunol 49:297-303
Chatterjee, Sanjukta; Ju, Zhongliang; Hassan, Rabih et al. (2011) Dynamic changes in binding of immunoglobulin heavy chain 3' regulatory region to protein factors during class switching. J Biol Chem 286:29303-12
Degner, Stephanie C; Verma-Gaur, Jiyoti; Wong, Timothy P et al. (2011) CCCTC-binding factor (CTCF) and cohesin influence the genomic architecture of the Igh locus and antisense transcription in pro-B cells. Proc Natl Acad Sci U S A 108:9566-71
Yan, Yi; Pieretti, Joyce; Ju, Zhongliang et al. (2011) Homologous elements hs3a and hs3b in the 3' regulatory region of the murine immunoglobulin heavy chain (Igh) locus are both dispensable for class-switch recombination. J Biol Chem 286:27123-31
Frezza, D; Giambra, V; Mattioli, C et al. (2009) Allelic frequencies of 3' Ig heavy chain locus enhancer HS1,2-A associated with Ig levels in patients with schizophrenia. Int J Immunopathol Pharmacol 22:115-23
Giambra, Vincenzo; Volpi, Sabrina; Emelyanov, Alexander V et al. (2008) Pax5 and linker histone H1 coordinate DNA methylation and histone modifications in the 3'regulatory region of the immunoglobulin heavy chain locus. Mol Cell Biol 28:6123-33

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