| First Author | Gupta-Rossi N | Year | 2003 |
| Journal | Mol Immunol | Volume | 39 |
| Issue | 13 | Pages | 791-9 |
| PubMed ID | 12617994 | Mgi Jnum | J:87056 |
| Mgi Id | MGI:2683129 | Doi | 10.1016/s0161-5890(03)00002-6 |
| Citation | Gupta-Rossi N, et al. (2003) Specific over-expression of deltex and a new Kelch-like protein in human germinal center B cells. Mol Immunol 39(13):791-9 |
| abstractText | Ig gene hypermutation was originally described as the molecular process underlying B cell affinity maturation following a T-dependent immune response. Somatic hypermutation is also used in some species such as sheep, to generate diversity during formation of the primary antibody repertoire. In sheep, B cells mutate their Ig receptor during antigen-independent development in the lymphoid follicles of ileal Peyer's patches, but this process is arrested when these same B cells are cultured in vitro. We have used these differences between in vivo and in vitro B cell development to perform a cDNA subtraction between these two cell populations, in order to search for genes that might be involved in the hypermutation process. We describe in this paper the characterization of two genes, highly expressed in sheep ileal Peyer's patch B cells and also in centroblasts of human tonsils: deltex (Drosophila) homolog 1 (DTX1), which is related to the Notch pathway and a new Kelch-like protein, KLHL6. The putative role of these proteins, which are more likely involved in the germinal center B cell differentiation pathway than in the hypermutation mechanism per se, is discussed. |
