B cell development arrest upon insertion of a neo gene between JH and Eμ:: Promoter competition results in transcriptional silencing of germline JH and complete V(D)J rearrangements

被引:20
作者
Delpy, L
Decourt, C
Le Bert, M
Cogné, M
机构
[1] Fac Med, Immunol Lab, CNRS, UMR 6101, F-87025 Limoges, France
[2] CNRS, Ctr Dev Tech Avancees Expt Anim, F-45071 Orleans, France
关键词
D O I
10.4049/jimmunol.169.12.6875
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Previous targeting experiments within the IgH locus have shown that V(D)J recombination was affected by an insertion of a neo gene within Emu upstream of the core enhancer, but not by insertions downstream of the enhancer. Similarly, class switch recombination to a given (C) gene was affected only by interposition of neo in between that gene and the 3' IgH enhancers. Here we show that insertion of neo upstream Emu only marginally impairs V(D)J recombination, but results in an altered D and J(H) gene usage and completely blocks transcription of the germline J(H) region and the rearranged VDJ segments. Although transcriptional silencing of J(H) occurs upstream of the insertion and results in the lack of mature B cells in homozygous mutant animals, IgH transcription is maintained downstream of the insertion together with neo transcription and can be up-regulated by LPS stimulation or upon fusion with plasmacytoma cells. Altogether these data argue for a polarized "neo effect" involving promoter competition and further show that V(D)J rearrangement can, be uncoupled from transcription.
引用
收藏
页码:6875 / 6882
页数:8
相关论文
共 29 条
[21]   Heavy and light chain primary structures control IgG3 nephritogenicity in an experimental model for cryocrystalglobulinemia [J].
Rengers, JU ;
Touchard, G ;
Decourt, C ;
Deret, S ;
Michel, H ;
Cogné, M .
BLOOD, 2000, 95 (11) :3467-3472
[22]   Recombination and transcription of the endogenous Ig heavy chain locus is effected by the Ig heavy chain intronic enhancer core region in the absence of the matrix attachment regions [J].
Sakai, E ;
Bottaro, A ;
Davidson, L ;
Sleckman, BP ;
Alt, FW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (04) :1526-1531
[23]   VIRUS-TRANSFORMED PRE-B CELLS SHOW ORDERED ACTIVATION BUT NOT INACTIVATION OF IMMUNOGLOBULIN GENE REARRANGEMENT AND TRANSCRIPTION [J].
SCHLISSEL, MS ;
CORCORAN, LM ;
BALTIMORE, D .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (03) :711-720
[24]   Position-dependent inhibition of class-switch recombination by PGK-neor cassettes inserted into the immunoglobulin heavy chain constant region locus [J].
Seidl, KJ ;
Manis, JP ;
Bottaro, A ;
Zhang, J ;
Davidson, L ;
Kisselgof, A ;
Oettgen, H ;
Alt, FW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (06) :3000-3005
[25]   V(D)J RECOMBINATION IN B-CELLS IS IMPAIRED BUT NOT BLOCKED BY TARGETED DELETION OF THE IMMUNOGLOBULIN HEAVY-CHAIN INTRON ENHANCER [J].
SERWE, M ;
SABLITZKY, F .
EMBO JOURNAL, 1993, 12 (06) :2321-2327
[26]   Chromatin structure and gene regulation in the immune system [J].
Smale, ST ;
Fisher, AG .
ANNUAL REVIEW OF IMMUNOLOGY, 2002, 20 :427-462
[27]   Insertion of phosphoglycerine kinase (PGK)-Neo 5′ of Jλ1 dramatically enhances VJλ1 rearrangement [J].
Sun, T ;
Storb, U .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 193 (06) :699-711
[28]   DEVELOPMENTALLY CONTROLLED AND TISSUE-SPECIFIC EXPRESSION OF UNREARRANGED VH GENE SEGMENTS [J].
YANCOPOULOS, GD ;
ALT, FW .
CELL, 1985, 40 (02) :271-281
[29]   Truncation of the μ heavy chain alters BCR signalling and allows recruitment of CD5+ B cells [J].
Zou, XG ;
Ayling, C ;
Xian, J ;
Piper, TA ;
Barker, PJ ;
Brüggemann, M .
INTERNATIONAL IMMUNOLOGY, 2001, 13 (12) :1489-1499