Literature DB >> 1644296

The basis for the mechanistic bias for deletional over inversional V(D)J recombination.

G H Gauss1, M R Lieber.   

Abstract

V(D)J recombination between recognition sites in the genome is characterized by certain biases. At some loci, proximal sites undergo recombination substantially more frequently than distal ones. The joining of DH/JH is an example of this. Because the DH element bears signal sequences on each side, inversion would be expected as often as deletion in DH/JH recombination. However, the markedly favored outcome is deletion, entailing utilization of the closer recombination site. One model proposed to explain these biases is the tracking model in which the recombinase tracks from one site to the other. Here, we have directly tested for various types of tracking in V(D)J recombination and have found no indication that it occurs. In addition, we have created DH-JH minilocus substrates for analysis of the basis for the preference for deletion. We find that we can reproduce the deletional bias for the system. Moreover, by flipping the orientation of the D segment, we can reverse the bias such that the frequency of inversions can exceed the number of deletions. These results indicate (1) that there is no intrinsic topological preference in this reaction, and (2) that the sequence of the signal and coding ends determines the bias.

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Year:  1992        PMID: 1644296     DOI: 10.1101/gad.6.8.1553

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  25 in total

1.  Postcleavage sequence specificity in V(D)J recombination.

Authors:  E A Agard; S M Lewis
Journal:  Mol Cell Biol       Date:  2000-07       Impact factor: 4.272

Review 2.  Factors that influence formation of B cell repertoire.

Authors:  A J Feeney
Journal:  Immunol Res       Date:  2000       Impact factor: 2.829

3.  Both V(D)J coding ends but neither signal end can recombine at the bcl-2 major breakpoint region, and the rejoining is ligase IV dependent.

Authors:  Sathees C Raghavan; Chih-Lin Hsieh; Michael R Lieber
Journal:  Mol Cell Biol       Date:  2005-08       Impact factor: 4.272

4.  No evidence for the use of DIR, D-D fusions, chromosome 15 open reading frames or VH replacement in the peripheral repertoire was found on application of an improved algorithm, JointML, to 6329 human immunoglobulin H rearrangements.

Authors:  Line Ohm-Laursen; Morten Nielsen; Stine R Larsen; Torben Barington
Journal:  Immunology       Date:  2006-10       Impact factor: 7.397

5.  Regulation of repertoire development through genetic control of DH reading frame preference.

Authors:  Michael Zemlin; Robert L Schelonka; Gregory C Ippolito; Cosima Zemlin; Yingxin Zhuang; G Larry Gartland; Lars Nitschke; Jukka Pelkonen; Klaus Rajewsky; Harry W Schroeder
Journal:  J Immunol       Date:  2008-12-15       Impact factor: 5.422

6.  Genetic evidence that the RAG1 protein directly participates in V(D)J recombination through substrate recognition.

Authors:  C A Roman; D Baltimore
Journal:  Proc Natl Acad Sci U S A       Date:  1996-03-19       Impact factor: 11.205

7.  Mouse RSS spacer sequences affect the rate of V(D)J recombination.

Authors:  L Fanning; A Connor; K Baetz; D Ramsden; G E Wu
Journal:  Immunogenetics       Date:  1996       Impact factor: 2.846

8.  Molecular mechanisms and selective influences that shape the kappa gene repertoire of IgM+ B cells.

Authors:  S J Foster; H P Brezinschek; R I Brezinschek; P E Lipsky
Journal:  J Clin Invest       Date:  1997-04-01       Impact factor: 14.808

9.  Evolutionarily conserved pattern of gene segment usage within the mammalian TCRbeta locus.

Authors:  Ferenc Livák
Journal:  Immunogenetics       Date:  2003-07-04       Impact factor: 2.846

10.  A role for XLF in DNA repair and recombination in human somatic cells.

Authors:  Farjana Jahan Fattah; Junghun Kweon; Yongbao Wang; Eu Han Lee; Yinan Kan; Natalie Lichter; Natalie Weisensel; Eric A Hendrickson
Journal:  DNA Repair (Amst)       Date:  2014-01-21
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