Literature DB >> 8413286

V(D)J recombination coding junction formation without DNA homology: processing of coding termini.

N V Boubnov1, Z P Wills, D T Weaver.   

Abstract

Coding junction formation in V(D)J recombination generates diversity in the antigen recognition structures of immunoglobulin and T-cell receptor molecules by combining processes of deletion of terminal coding sequences and addition of nucleotides prior to joining. We have examined the role of coding end DNA composition in junction formation with plasmid substrates containing defined homopolymers flanking the recombination signal sequence elements. We found that coding junctions formed efficiently with or without terminal DNA homology. The extent of junctional deletion was conserved independent of coding ends with increased, partial, or no DNA homology. Interestingly, G/C homopolymer coding ends showed reduced deletion regardless of DNA homology. Therefore, DNA homology cannot be the primary determinant that stabilizes coding end structures for processing and joining.

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Year:  1993        PMID: 8413286      PMCID: PMC364757          DOI: 10.1128/mcb.13.11.6957-6968.1993

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  37 in total

1.  Predominance of VH-D-JH junctions occurring at sites of short sequence homology results in limited junctional diversity in neonatal antibodies.

Authors:  A J Feeney
Journal:  J Immunol       Date:  1992-07-01       Impact factor: 5.422

Review 2.  Site-specific recombination in the immune system.

Authors:  M R Lieber
Journal:  FASEB J       Date:  1991-11       Impact factor: 5.191

3.  V(D)J recombination: signal and coding joint resolution are uncoupled and depend on parallel synapsis of the sites.

Authors:  K M Sheehan; M R Lieber
Journal:  Mol Cell Biol       Date:  1993-03       Impact factor: 4.272

4.  Impairment of V(D)J recombination in double-strand break repair mutants.

Authors:  G E Taccioli; G Rathbun; E Oltz; T Stamato; P A Jeggo; F W Alt
Journal:  Science       Date:  1993-04-09       Impact factor: 47.728

5.  P nucleotides in V(D)J recombination: a fine-structure analysis.

Authors:  J T Meier; S M Lewis
Journal:  Mol Cell Biol       Date:  1993-02       Impact factor: 4.272

6.  V(D)J recombination in mammalian cell mutants defective in DNA double-strand break repair.

Authors:  F Pergola; M Z Zdzienicka; M R Lieber
Journal:  Mol Cell Biol       Date:  1993-06       Impact factor: 4.272

7.  Extent to which homology can constrain coding exon junctional diversity in V(D)J recombination.

Authors:  R M Gerstein; M R Lieber
Journal:  Nature       Date:  1993-06-17       Impact factor: 49.962

8.  Lack of N regions in antigen receptor variable region genes of TdT-deficient lymphocytes.

Authors:  T Komori; A Okada; V Stewart; F W Alt
Journal:  Science       Date:  1993-08-27       Impact factor: 47.728

9.  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

10.  Selection is not required to produce invariant T-cell receptor gamma-gene junctional sequences.

Authors:  D M Asarnow; D Cado; D H Raulet
Journal:  Nature       Date:  1993-03-11       Impact factor: 49.962

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  13 in total

1.  Mechanistic basis for coding end sequence effects in the initiation of V(D)J recombination.

Authors:  K Yu; M R Lieber
Journal:  Mol Cell Biol       Date:  1999-12       Impact factor: 4.272

2.  The presence of direct repeats does not influence coding joint formation during V(D)J recombination.

Authors:  F Nourrit; Q T Nguyen; F Rougeon; S Kallenbach
Journal:  Nucleic Acids Res       Date:  1996-10-15       Impact factor: 16.971

3.  Nucleotide deletion and P addition in V(D)J recombination: a determinant role of the coding-end sequence.

Authors:  B Nadel; A J Feeney
Journal:  Mol Cell Biol       Date:  1997-07       Impact factor: 4.272

4.  The composition of coding joints formed in V(D)J recombination is strongly affected by the nucleotide sequence of the coding ends and their relationship to the recombination signal sequences.

Authors:  U R Ezekiel; T Sun; G Bozek; U Storb
Journal:  Mol Cell Biol       Date:  1997-07       Impact factor: 4.272

5.  Hairpin opening by single-strand-specific nucleases.

Authors:  E B Kabotyanski; C Zhu; D A Kallick; D B Roth
Journal:  Nucleic Acids Res       Date:  1995-10-11       Impact factor: 16.971

6.  Coding sequence composition flanking either signal element alters V(D)J recombination efficiency.

Authors:  N V Boubnov; Z P Wills; D T Weaver
Journal:  Nucleic Acids Res       Date:  1995-03-25       Impact factor: 16.971

7.  scid cells efficiently integrate hairpin and linear DNA substrates.

Authors:  J E Staunton; D T Weaver
Journal:  Mol Cell Biol       Date:  1994-06       Impact factor: 4.272

8.  Complementation of the ionizing radiation sensitivity, DNA end binding, and V(D)J recombination defects of double-strand break repair mutants by the p86 Ku autoantigen.

Authors:  N V Boubnov; K T Hall; Z Wills; S E Lee; D M He; D M Benjamin; C R Pulaski; H Band; W Reeves; E A Hendrickson
Journal:  Proc Natl Acad Sci U S A       Date:  1995-01-31       Impact factor: 11.205

9.  Requirement for the kinase activity of human DNA-dependent protein kinase catalytic subunit in DNA strand break rejoining.

Authors:  A Kurimasa; S Kumano; N V Boubnov; M D Story; C S Tung; S R Peterson; D J Chen
Journal:  Mol Cell Biol       Date:  1999-05       Impact factor: 4.272

10.  Mechanistic constraints on diversity in human V(D)J recombination.

Authors:  G H Gauss; M R Lieber
Journal:  Mol Cell Biol       Date:  1996-01       Impact factor: 4.272

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