Position-dependent inhibition of class-switch recombination by PGK-neor cassettes inserted into the immunoglobulin heavy chain constant region locus.

The Ig heavy chain (IgH) constant region (CH) genes are organized from 5' to 3' in the order Cmicro, Cdelta, Cgamma3, Cgamma1, Cgamma2b, Cgamma2a, Cepsilon, and Calpha. Expression of CH genes downstream of Cdelta involves class-switch recombination (CSR), a process that is targeted by germ-line transcription (GT) of the corresponding CH gene. Previously, we demonstrated that insertion of a PGK-neor cassette at two sites downstream of Calpha inhibits, in cultured B cells, GT of and CSR to a subset of CH genes (including Cgamma3, Cgamma2a, Cgamma2b, and Cepsilon) that lie as far as 120 kb upstream. Here we show that insertion of the PGK-neor cassette in place of sequences in the Igamma2b locus inhibits GT of and CSR to the upstream Cgamma3 gene, but has no major effect on the downstream Cgamma2a and Cepsilon genes. Moreover, replacement of the Cepsilon exons with a PGK-neor cassette in the opposite transcriptional orientation also inhibits, in culture, GT of and CSR to the upstream Cgamma3, Cgamma2b, and Cgamma2a genes. As with the PGK-neor insertions 3' of Calpha studied previously, the Cgamma1 and Calpha genes were less affected by these mutations both in culture and in mice, whereas the Cgamma2b gene appeared less affected in vivo. Our findings support the existence of a long-range 3' IgH regulatory region required for GT of and CSR to multiple CH genes and suggest that PGK-neor cassette insertion into the locus short circuits the ability of this region to facilitate GT of dependent CH genes upstream of the insertion.

[1]  M. Wabl,et al.  Expression of immunoglobulin heavy chain at a high level in the absence of a proposed immunoglobulin enhancer element in cis. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[2]  L. Eckhardt,et al.  Independent immunoglobulin class-switch events occurring in a single myeloma cell line , 1985, Molecular and cellular biology.

[3]  M. Hummel,et al.  Switch region content of hybridomas: the two spleen cell Igh loci tend to rearrange to the same isotype. , 1987, Journal of immunology.

[4]  F. Alt,et al.  Structure and expression of germ line immunoglobulin gamma 2b transcripts , 1988, Molecular and cellular biology.

[5]  M. Neuberger,et al.  A second B cell-specific enhancer 3' of the immunoglobulin heavy-chain locus , 1990, Nature.

[6]  V. Stewart,et al.  Structure and expression of germline immunoglobulin gamma 3 heavy chain gene transcripts: implications for mitogen and lymphokine directed class-switching. , 1990, International immunology.

[7]  C. Pinkert,et al.  A strain-specific modifier on mouse chromosome 4 controls the methylation of independent transgene loci , 1991, Cell.

[8]  L. Eckhardt,et al.  An enhancer at the 3' end of the mouse immunoglobulin heavy chain locus. , 1991, Nucleic acids research.

[9]  M. Neuberger,et al.  The mouse IgH 3′‐enhancer , 1991, European journal of immunology.

[10]  P. Leder,et al.  Humoral immune functions in IL-4 transgenic mice. , 1991, Journal of immunology.

[11]  H. Hauser,et al.  The prokaryotic neomycin-resistance-encoding gene acts as a transcriptional silencer in eukaryotic cells. , 1991, Gene.

[12]  W. C. Forrester,et al.  Inactivation of the human beta-globin gene by targeted insertion into the beta-globin locus control region. , 1992, Genes & development.

[13]  R. Krumlauf,et al.  Hoxb-4 (Hox-2.6) mutant mice show homeotic transformation of a cervical vertebra and defects in the closure of the sternal rudiments , 1993, Cell.

[14]  F. Alt,et al.  Replacement of germ-line epsilon promoter by gene targeting alters control of immunoglobulin heavy chain class switching. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[15]  The immunoglobulin heavy chain locus contains another B-cell-specific 3' enhancer close to the alpha constant region. , 1993, Molecular and cellular biology.

[16]  M. Groudine,et al.  An "in-out" strategy using gene targeting and FLP recombinase for the functional dissection of complex DNA regulatory elements: analysis of the beta-globin locus control region. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[17]  K. Rajewsky,et al.  Deletion of the immunoglobulin kappa chain intron enhancer abolishes kappa chain gene rearrangement in cis but not lambda chain gene rearrangement in trans. , 1993, The EMBO journal.

[18]  K. Rajewsky,et al.  Shutdown of class switch recombination by deletion of a switch region control element , 1993, Science.

[19]  V. Stewart,et al.  A selective defect in IgG2b switching as a result of targeted mutation of the I gamma 2b promoter and exon. , 1993, The EMBO journal.

[20]  R. Coffman,et al.  Mechanism and regulation of immunoglobulin isotype switching. , 1993, Advances in immunology.

[21]  C. Snapper,et al.  Towards a comprehensive view of immunoglobulin class switching. , 1993, Immunology today.

[22]  K. Rajewsky,et al.  Independent control of immunoglobulin switch recombination at individual switch regions evidenced through Cre-loxP-mediated gene targeting , 1993, Cell.

[23]  Andreas Radbruch,et al.  Frequency of immunoglobulin E class switching is autonomously determined and independent of prior switching to other classes , 1994, The Journal of experimental medicine.

[24]  F. Alt,et al.  S region transcription per se promotes basal IgE class switch recombination but additional factors regulate the efficiency of the process. , 1994, The EMBO journal.

[25]  L. Madisen,et al.  Identification of a locus control region in the immunoglobulin heavy-chain locus that deregulates c-myc expression in plasmacytoma and Burkitt's lymphoma cells. , 1994, Genes & development.

[26]  P. Leder,et al.  Active anaphylaxis in IgE-deficient mice , 1994, Nature.

[27]  F. Alt,et al.  A class switch control region at the 3′ end of the immunoglobulin heavy chain locus , 1994, Cell.

[28]  T. Braun,et al.  Inactivation of Myf‐6 and Myf‐5 genes in mice leads to alterations in skeletal muscle development. , 1995, The EMBO journal.

[29]  T. Ley,et al.  Targeted deletion of 5'HS2 of the murine beta-globin LCR reveals that it is not essential for proper regulation of the beta-globin locus. , 1995, Genes & development.

[30]  Andreas Radbruch,et al.  Switch transcripts in immunoglobulin class switching. , 1995, Science.

[31]  F. Alt,et al.  The Igκ 3′ Enhancer Influences the Ratio of Igκ versus Igλ B Lymphocytes , 1996 .

[32]  J. Stavnezer Immunoglobulin class switching. , 1996, Current opinion in immunology.

[33]  M. Groudine,et al.  Regulation of β-globin gene expression: straightening out the locus , 1996 .

[34]  T. Ley,et al.  Long-range disruption of gene expression by a selectable marker cassette. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[35]  T. Ley,et al.  Analysis of mice containing a targeted deletion of beta-globin locus control region 5' hypersensitive site 3 , 1996, Molecular and cellular biology.

[36]  A. Bradley,et al.  IgA class switch in I alpha exon-deficient mice. Role of germline transcription in class switch recombination. , 1996, The Journal of clinical investigation.

[37]  F. Alt,et al.  Deletion of the Igκ Light Chain Intronic Enhancer/Matrix Attachment Region Impairs but Does Not Abolish VκJκ Rearrangement , 1996 .

[38]  F. Alt,et al.  Gene-targeted deletion and replacement mutations of the T-cell receptor beta-chain enhancer: the role of enhancer elements in controlling V(D)J recombination accessibility. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[39]  F. Alt,et al.  Function of the TCRα Enhancer in αβ and γδ T Cells , 1997 .

[40]  S. Orkin,et al.  A lineage‐selective knockout establishes the critical role of transcription factor GATA‐1 in megakaryocyte growth and platelet development , 1997, The EMBO journal.

[41]  R. D. Little,et al.  Murine and human 3'IgH regulatory sequences. , 1997, Current topics in microbiology and immunology.

[42]  J. Strouboulis,et al.  The effect of distance on long-range chromatin interactions. , 1997, Molecular cell.

[43]  S. Tilghman,et al.  Igf2 imprinting does not require its own DNA methylation or H19 RNA. , 1998, Genes & development.

[44]  Jianzhu Chen,et al.  Enhanced B-1 cell development, but impaired IgG antibody responses in mice deficient in secreted IgM. , 1998, Journal of immunology.

[45]  D. Higgs Do LCRs Open Chromatin Domains? , 1998, Cell.

[46]  F. Alt,et al.  Class Switching in B Cells Lacking 3′ Immunoglobulin Heavy Chain Enhancers , 1998, The Journal of experimental medicine.

[47]  M. Groudine,et al.  The β-Globin LCR Is Not Necessary for an Open Chromatin Structure or Developmentally Regulated Transcription of the Native Mouse β-Globin Locus , 1998 .

[48]  F. Alt,et al.  Deletion of the IgH intronic enhancer and associated matrix-attachment regions decreases, but does not abolish, class switching at the mu locus. , 1998, International immunology.

[49]  R. Roeder,et al.  3' IgH enhancer elements shift synergistic interactions during B cell development. , 1998, Journal of immunology.

[50]  J. Stavnezer,et al.  Iα exon-replacement mice synthesize a spliced HPRT–Cα transcript which may explain their ability to switch to IgA. Inhibition of switching to IgG in these mice , 1999 .