Literature DB >> 3135329

Abnormal recombination of Igh D and J gene segments in transformed pre-B cells of scid mice.

M G Kim1, W Schuler, M J Bosma, K B Marcu.   

Abstract

Studies of Ig and TCR genes in transformed lymphocytes of scid mice have revealed aberrant DNA rearrangements. Here we present a more detailed analysis of the Igh gene recombination in nine scid pre-B cell lines transformed by Abelson murine leukemia virus. We found 85% of the rearranged Igh alleles to contain abnormal Dh-Jh deletions of varying size. All of these deletions encompassed Jh elements and extended into the Igh enhancer region, occasionally involving the switch (S) region of the C mu gene. Some of these rearrangements removed most of the Dh elements, but none appeared to extend to the Vh genes. DNA sequence analysis of the two abnormally rearranged Igh alleles in one pre-B cell line showed that no Dh or Jh coding sequences were retained at the recombination sites though heptamer-like (CACTGTG) recognition signal sequences were present in the absence of nonamer (GGTTTTTGT) recognition signal sequences. These results imply that a deregulated recombinase activity may be responsible for the abnormal Dh-Jh deletions and the absence of Vh-Dh joining in established lines of Abelson murine leukemia virus-transformed scid pre-B cells.

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Year:  1988        PMID: 3135329

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  19 in total

Review 1.  SCID mice in the study of human autoimmune diseases.

Authors:  M A Duchosal
Journal:  Springer Semin Immunopathol       Date:  1992

2.  Strand breaks without DNA rearrangement in V (D)J recombination.

Authors:  E A Hendrickson; V F Liu; D T Weaver
Journal:  Mol Cell Biol       Date:  1991-06       Impact factor: 4.272

3.  Wild-type V(D)J recombination in scid pre-B cells.

Authors:  E A Hendrickson; M S Schlissel; D T Weaver
Journal:  Mol Cell Biol       Date:  1990-10       Impact factor: 4.272

4.  Efficient nonhomologous and homologous recombination in scid cells.

Authors:  B Bühler; G Köhler; P J Nielsen
Journal:  Immunogenetics       Date:  1995       Impact factor: 2.846

5.  Hemagglutination and graft-versus-host disease in the severe combined immunodeficiency mouse lymphoproliferative disease model.

Authors:  S J Pirruccello; H Nakamine; K W Beisel; K L Kleveland; M Okano; Y Taguchi; J R Davis; M L Mahloch; D T Purtilo
Journal:  Am J Pathol       Date:  1992-05       Impact factor: 4.307

6.  The mouse mutation severe combined immune deficiency (scid) is on chromosome 16.

Authors:  G C Bosma; M T Davisson; N R Ruetsch; H O Sweet; L D Shultz; M J Bosma
Journal:  Immunogenetics       Date:  1989       Impact factor: 2.846

7.  Biased T-cell receptor delta element recombination in scid thymocytes.

Authors:  A M Carroll; J K Slack; W T Chang
Journal:  Mol Cell Biol       Date:  1993-06       Impact factor: 4.272

8.  Analysis of the defect in DNA end joining in the murine scid mutation.

Authors:  J Harrington; C L Hsieh; J Gerton; G Bosma; M R Lieber
Journal:  Mol Cell Biol       Date:  1992-10       Impact factor: 4.272

Review 9.  The SCID mouse: relevance as an animal model system for studying human disease.

Authors:  E A Hendrickson
Journal:  Am J Pathol       Date:  1993-12       Impact factor: 4.307

10.  Development of B-lineage cells in the bone marrow of scid/scid mice following the introduction of functionally rearranged immunoglobulin transgenes.

Authors:  M Reichman-Fried; R R Hardy; M J Bosma
Journal:  Proc Natl Acad Sci U S A       Date:  1990-04       Impact factor: 11.205

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