The overall goal of the proposed research will be to characterize, in a molecular and biological fashion, the genes encoding the members of the murine and human (CR1) gene family. This gene family include the CR1 and CR2 genes, and two new, previously undescribed gene. Additionally, the chromosomal location of human CR1 will be examined in relation to other linked genes sharing amino acid and nucleic acid homology to CR1. The mouse genome appears to contain at least four CR1/CR1- related genes which are expressed as mRNA transcripts in a variety of different tissues. The primary objective will be to clone and at least partially, if not completely, sequence these four genes and to characterize both biochemically and biologically the proteins encoded by these distinct genes. One of these genes is likely to be murine CR1 due to its tissue specific expression, nucleic acid homology to human CR1, and the size of it transcript. The other two genes appear not to encode CR1 or CR2, but instead two proteins expressed in tissues which suggest that they mat by either DAF or gp45-70, or other uncharacterized proteins. The proteins encoded by the CR1 gene family will be identified by: (i) using the cDNA sequences to produce recombinant protein in E. coli., (ii) using the recombinant protein to generate polyclonal antisera against the peptide sequence, (iii) analyzing the murine proteins identified by these antisera, and presuming the CR1-related genes share CR1/CR2-like activities, (iv) blocking the functions of the murine proteins by antibody binding, and (v) identifying the protein products of these genes by transfecting studies using the entire gene in either phage or cosmid vectors. Once the murine CR1-related genes have been identified, the human homologues will also be isolated and characterized. The linkage of the murine CR1 gene on murine chromosome 1 to SLE genes on chromosome 1 (gld and the NZB- linked SLE gene) will also be evaluated. The molecular linkage of human CR1, C4bp, and H, and perhaps the human homologue of the murine CR1-related gene Y, on human chromosome 1 will identify the second major complement protein locus (the C4 locus in the MHC would be the first) in the genome. The structure of the CR1 gene associated with the genetic instability of the region of the chromosome to which the CR1 gene maps suggests a mechanism for chromosomal instability which will be investigated.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
1R01AI024158-01
Application #
3136912
Study Section
Allergy and Immunology Study Section (ALY)
Project Start
1986-12-01
Project End
1989-11-30
Budget Start
1986-12-01
Budget End
1987-11-30
Support Year
1
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
071723621
City
Boston
State
MA
Country
United States
Zip Code
02115
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Donius, Luke R; Orlando, Christopher M; Weis, Janis J et al. (2014) Generation of a novel Cr2 gene allele by homologous recombination that abrogates production of Cr2 but is sufficient for expression of Cr1. Immunobiology 219:53-63
Pioli, Peter D; Debnath, Irina; Weis, Janis J et al. (2014) Zfp318 regulates IgD expression by abrogating transcription termination within the Ighm/Ighd locus. J Immunol 193:2546-53
Pioli, Peter D; Weis, John H (2014) Snail transcription factors in hematopoietic cell development: a model of functional redundancy. Exp Hematol 42:425-30
Debnath, Irina; Roundy, Kirstin M; Pioli, Peter D et al. (2013) Bone marrow-induced Mef2c deficiency delays B-cell development and alters the expression of key B-cell regulatory proteins. Int Immunol 25:99-115
Pioli, Peter D; Dahlem, Timothy J; Weis, Janis J et al. (2013) Deletion of Snai2 and Snai3 results in impaired physical development compounded by lymphocyte deficiency. PLoS One 8:e69216
Donius, Luke R; Handy, Jennifer M; Weis, Janis J et al. (2013) Optimal germinal center B cell activation and T-dependent antibody responses require expression of the mouse complement receptor Cr1. J Immunol 191:434-47
Dahlem, Timothy; Cho, Scott; Spangrude, Gerald J et al. (2012) Overexpression of Snai3 suppresses lymphoid- and enhances myeloid-cell differentiation. Eur J Immunol 42:1038-43
Bramwell, Kenneth K C; Ma, Ying; Weis, John H et al. (2012) High-throughput genotyping of advanced congenic lines by high resolution melting analysis for identification of Bbaa2, a QTL controlling Lyme arthritis. Biotechniques 52:183-90
Lochhead, Robert B; Sonderegger, F Lynn; Ma, Ying et al. (2012) Endothelial cells and fibroblasts amplify the arthritogenic type I IFN response in murine Lyme disease and are major sources of chemokines in Borrelia burgdorferi-infected joint tissue. J Immunol 189:2488-501

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