Neoteny in Lymphocytes: Rag1 and Rag2 Expression in Germinal Center B Cells
- 20 December 1996
- journal article
- other
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 274 (5295) , 2094-2097
- https://doi.org/10.1126/science.274.5295.2094
Abstract
The products of the Rag1 and Rag2 genes drive genomic V(D)J rearrangements that assemble functional immunoglobulin and T cell antigen receptor genes. Expression of the Rag genes has been thought to be limited to developmentally immature lymphocyte populations that in normal adult animals are primarily restricted to the bone marrow and thymus. Abundant RAG1 and RAG2 protein and messenger RNA was detected in the activated B cells that populate murine splenic and Peyer's patch germinal centers. Germinal center B cells thus share fundamental characteristics of immature lymphocytes, raising the possibility that antigen-dependent secondary V(D)J rearrangements modify the peripheral antibody repertoire.Keywords
This publication has 30 references indexed in Scilit:
- V(D)J recombination and the cell cycleImmunology Today, 1995
- Rabbit IgH sequences in appendix germinal centers: VH diversification by gene conversion-like and hypermutation mechanismsImmunity, 1994
- Germinal CentersAnnual Review of Immunology, 1994
- Clonal expansion in follicular lymphoma occurs subsequent to antigenic selection.The Journal of Experimental Medicine, 1992
- In situ studies of the primary immune response to (4-hydroxy-3-nitrophenyl)acetyl. II. A common clonal origin for periarteriolar lymphoid sheath-associated foci and germinal centers.The Journal of Experimental Medicine, 1992
- Among naive precursor cell subpopulations only progenitors of memory B cells originate germinal centersEuropean Journal of Immunology, 1992
- Maturation of the immune response in germinal centersCell, 1991
- Somatic diversification of the chicken immunoglobulin light chain gene is limited to the rearranged variable gene segmentCell, 1987
- Clustering of extensive somatic mutations in the variable region of an immunoglobulin heavy chain gene from a human B cell lymphomaCell, 1986
- Biclonal B-Cell LymphomaNew England Journal of Medicine, 1984