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
相关论文
共 39 条
  • [1] JOINING OF IMMUNOGLOBULIN HEAVY-CHAIN GENE SEGMENTS - IMPLICATIONS FROM A CHROMOSOME WITH EVIDENCE OF 3 D-JH FUSIONS
    ALT, FW
    BALTIMORE, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (13): : 4118 - 4122
  • [2] Two novel human and mouse DNA polymerases of the polX family
    Aoufouchi, S
    Flatter, E
    Dahan, A
    Faili, A
    Bertocci, B
    Storck, S
    Delbos, F
    Cocea, L
    Gupta, N
    Weill, JC
    Reynaud, CA
    [J]. NUCLEIC ACIDS RESEARCH, 2000, 28 (18) : 3684 - 3693
  • [3] The mechanism and regulation of chromosomal V(D)J recombination
    Bassing, CH
    Swat, W
    Alt, FW
    [J]. CELL, 2002, 109 : S45 - S55
  • [4] Bentolila LA, 1999, J IMMUNOL, V162, P2123
  • [5] Cutting edge:: DNA polymerases μ and λ are dispensable for Ig gene hypermutation
    Bertocci, B
    De Smet, A
    Flatter, E
    Dahan, A
    Bories, JC
    Landreau, C
    Weill, JC
    Reynaud, CA
    [J]. JOURNAL OF IMMUNOLOGY, 2002, 168 (08) : 3702 - 3706
  • [6] A superfamily of conserved domains in DNA damage responsive cell cycle checkpoint proteins
    Bork, P
    Hofmann, K
    Bucher, P
    Neuwald, AF
    Altschul, SF
    Koonin, EV
    [J]. FASEB JOURNAL, 1997, 11 (01) : 68 - 76
  • [7] Most α/β T cell receptor diversity is due to terminal deoxynucleotidyl transferase
    Cabaniols, JP
    Fazilleau, N
    Casrouge, A
    Kourilsky, P
    Kanellopoulos, JM
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 194 (09) : 1385 - 1390
  • [8] A targeted deletion of a region upstream from the Jκ cluster impairs κ chain rearrangement in cis in mice and in the 103/bc12 cell line
    Cocea, L
    De Smet, A
    Saghatchian, M
    Fillatreau, S
    Ferradini, L
    Schurmans, S
    Weill, JC
    Reynaud, CA
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (09) : 1443 - 1449
  • [9] INSERTION OF N REGIONS INTO HEAVY-CHAIN GENES IS CORRELATED WITH EXPRESSION OF TERMINAL DEOXYTRANSFERASE IN B-CELLS
    DESIDERIO, SV
    YANCOPOULOS, GD
    PASKIND, M
    THOMAS, E
    BOSS, MA
    LANDAU, N
    ALT, FW
    BALTIMORE, D
    [J]. NATURE, 1984, 311 (5988) : 752 - 755
  • [10] DNA polymerase mu (Pol μ), homologous to TdT, could act as a DNA mutator in eukaryotic cells
    Domínguez, O
    Ruiz, JF
    de Lera, TL
    García-Díaz, M
    González, MA
    Kirchhoff, T
    Martínez-A, C
    Bernad, A
    Blanco, L
    [J]. EMBO JOURNAL, 2000, 19 (07) : 1731 - 1742