Specific over-expression of deltex and a new Kelch-like protein in human germinal center B cells

被引:35
作者
Gupta-Rossi, N [1 ]
Storck, S [1 ]
Griebel, PJ [1 ]
Reynaud, CA [1 ]
Weill, JC [1 ]
Dahan, A [1 ]
机构
[1] Fac Med Necker Enfants Malad, INSERM, U373, F-75730 Paris 15, France
关键词
Ig gene hypermutation; Notch pathway; sheep ileal Peyer's patches;
D O I
10.1016/S0161-5890(03)00002-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:791 / 799
页数:9
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