Literature DB >> 10325418

The role of components of recombination signal sequences in immunoglobulin gene segment usage: a V81x model.

M Larijani1, C C Yu, R Golub, Q L Lam, G E Wu.   

Abstract

It has long been appreciated that some immunoglobulin (and T-cell receptor) gene segments are used much more frequently than others. The VHsegment V81x is a particularly striking case of overusage. Its usage varies with the stage of B-cell development and with the strain of mice, but it is always high in B cell progenitors. We have found that the coding sequence and the recombination signal sequences (RSS) are identical in five mouse strains, including CAST/Ei, a strain derived from the species Mus castaneus. Thus, the strain differences cannot be attributed to sequences within V81x itself. V81x RSS mediated recombination at rates significantly higher than another VHRSS. Although the V81x nonamer differs at one base pair from the consensus sequence, an RSS with this nonamer and a consensus heptamer recombines as well as the consensus RSS. When the V81x spacer is replaced by that of VA1, the frequency of recombination decreases by approximately 5-fold; thus, the contribution of variation in natural spacers to variability in VHusage in vivo is likely to be more than has been previously appreciated. Furthermore, the contribution of the heptamer and nonamer to differential VHusage in our assay is correlated inversely with their conservation throughout the VHlocus.

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Year:  1999        PMID: 10325418      PMCID: PMC148795          DOI: 10.1093/nar/27.11.2304

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  9 in total

Review 1.  Relative roles of somatic and Darwinian evolution in shaping the antibody response.

Authors:  M Diaz; N R Klinman
Journal:  Immunol Res       Date:  2000       Impact factor: 2.829

2.  Evolution of the recombination signal sequences in the Ig heavy-chain variable region locus of mammals.

Authors:  A Hassanin; R Golub; S M Lewis; G E Wu
Journal:  Proc Natl Acad Sci U S A       Date:  2000-10-10       Impact factor: 11.205

3.  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

4.  Evolution of the variable gene segments and recombination signal sequences of the human T-cell receptor alpha/delta locus.

Authors:  Marsha R Haynes; Gillian E Wu
Journal:  Immunogenetics       Date:  2004-09-18       Impact factor: 2.846

5.  Lack of MSH2 involvement differentiates V(D)J recombination from other non-homologous end joining events.

Authors:  Mani Larijani; Ahmad Zaheen; Darina Frieder; Yuxun Wang; Gillian E Wu; Winfried Edelmann; Alberto Martin
Journal:  Nucleic Acids Res       Date:  2005-11-27       Impact factor: 16.971

6.  Host genetics and diet, but not immunoglobulin A expression, converge to shape compositional features of the gut microbiome in an advanced intercross population of mice.

Authors:  Larry J Leamy; Scott A Kelly; Joseph Nietfeldt; Ryan M Legge; Fangrui Ma; Kunjie Hua; Rohita Sinha; Daniel A Peterson; Jens Walter; Andrew K Benson; Daniel Pomp
Journal:  Genome Biol       Date:  2014       Impact factor: 13.583

7.  Poor quality Vβ recombination signal sequences stochastically enforce TCRβ allelic exclusion.

Authors:  Glendon S Wu; Katherine S Yang-Iott; Morgann A Klink; Katharina E Hayer; Kyutae D Lee; Craig H Bassing
Journal:  J Exp Med       Date:  2020-09-07       Impact factor: 14.307

8.  A functional analysis of the spacer of V(D)J recombination signal sequences.

Authors:  Alfred Ian Lee; Sebastian D Fugmann; Lindsay G Cowell; Leon M Ptaszek; Garnett Kelsoe; David G Schatz
Journal:  PLoS Biol       Date:  2003-10-13       Impact factor: 8.029

9.  The kappa B transcriptional enhancer motif and signal sequences of V(D)J recombination are targets for the zinc finger protein HIVEP3/KRC: a site selection amplification binding study.

Authors:  Carl E Allen; Chi-ho Mak; Lai-Chu Wu
Journal:  BMC Immunol       Date:  2002-08-22       Impact factor: 3.615

  9 in total

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