Immunoglobulin κ light chain gene rearrangement is impaired in mice deficient for DNA polymerase mu

被引:117
作者
Bertocci, B
De Smet, A
Berek, C
Weill, JC
Reynaud, CA
机构
[1] Fac Med Necker Enfacts Malades, Inst Natl Francais Rech Med U373, F-75730 Paris 15, France
[2] Deutsch Rheumaforschungszentrum, D-10117 Berlin, Germany
关键词
D O I
10.1016/S1074-7613(03)00203-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
DNA polymerase mu (pol mu) is a template-dependent polymerase closely related to the lymphoid-specific enzyme terminal deoxynucleotidyl transferase (TdT). We report here the phenotype of pol mu-deficient mice. Such animals display an abnormal B cell differentiation, with a specific alteration in the IgM(-) to IgM(+) transition in bone marrow. In all mice, Ig light chain gene rearrangement is impaired at the level of the Vkappa-Jkappa and Vlambda-Jlambda junctions, which show extensive nibbling of both coding extremities. These alterations lead to a profound defect in the peripheral B cell compartment which, although variable between animals, results in an average 40% reduction in the splenic B cell fraction. Pol mu, appears, therefore, as a key element contributing to the relative homogeneity in size of light chain CDR3 and taking part in Ig gene rearrangement at a stage where TdT is no longer expressed.
引用
收藏
页码:203 / 211
页数:9
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