Literature DB >> 4053185

Trypanosoma brucei: the extent of conversion in antigen genes may be related to the DNA coding specificity.

E Pays, S Houard, A Pays, S Van Assel, F Dupont, D Aerts, G Huet-Duvillier, V Gomés, C Richet, P Degand.   

Abstract

The boundaries of gene conversion in variant-specific antigen genes have been determined in six clones of Trypanosoma brucei. In each clone, antigenic switching involved interaction between two telomeric members of the AnTat 1.1 multigene family, which share extensive homology throughout their coding regions. All conversion events occurred by substitution of faithful copies of donor sequences. Conversion endpoints were nonrandomly distributed. In four clones, the 5' conversion limit was near the antigen translation initiation codon, while in three clones, the 3' conversion limit was located at the "hinge" between the two major antigen domains. In one case, two segmental conversions were involved in antigen switching. These observations reveal that antigen gene conversion can occur without generating point mutations, and suggest that postrecombinational selection may impose a limit on the number of possible rearrangements within antigen genes.

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Year:  1985        PMID: 4053185     DOI: 10.1016/0092-8674(85)90278-8

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  14 in total

1.  Gene conversion in the Escherichia coli RecF pathway: a successive half crossing-over model.

Authors:  K Yamamoto; K Kusano; N K Takahashi; H Yoshikura; I Kobayashi
Journal:  Mol Gen Genet       Date:  1992-07

2.  Active late-appearing variable surface antigen genes in Trypanosoma equiperdum are constructed entirely from pseudogenes.

Authors:  C Roth; F Bringaud; R E Layden; T Baltz; H Eisen
Journal:  Proc Natl Acad Sci U S A       Date:  1989-12       Impact factor: 11.205

3.  Metacyclic variant surface glycoprotein genes of Trypanosoma brucei subsp. rhodesiense are activated in situ, and their expression is transcriptionally regulated.

Authors:  M J Lenardo; K M Esser; A M Moon; L H Van der Ploeg; J E Donelson
Journal:  Mol Cell Biol       Date:  1986-06       Impact factor: 4.272

4.  Characterization of the ligand-binding site of the transferrin receptor in Trypanosoma brucei demonstrates a structural relationship with the N-terminal domain of the variant surface glycoprotein.

Authors:  D Salmon; J Hanocq-Quertier; F Paturiaux-Hanocq; A Pays; P Tebabi; D P Nolan; A Michel; E Pays
Journal:  EMBO J       Date:  1997-12-15       Impact factor: 11.598

5.  Analysis of the VSG gene silent archive in Trypanosoma brucei reveals that mosaic gene expression is prominent in antigenic variation and is favored by archive substructure.

Authors:  Lucio Marcello; J David Barry
Journal:  Genome Res       Date:  2007-07-25       Impact factor: 9.043

Review 6.  Control of gene expression in trypanosomes.

Authors:  L Vanhamme; E Pays
Journal:  Microbiol Rev       Date:  1995-06

7.  Sequence-dependent gene conversion: can duplicated genes diverge fast enough to escape conversion?

Authors:  J B Walsh
Journal:  Genetics       Date:  1987-11       Impact factor: 4.562

8.  Homologous recombination in Leishmania enriettii.

Authors:  J F Tobin; A Laban; D F Wirth
Journal:  Proc Natl Acad Sci U S A       Date:  1991-02-01       Impact factor: 11.205

9.  The use of incomplete genes for the construction of a Trypanosoma equiperdum variant surface glycoprotein gene.

Authors:  C W Roth; S Longacre; A Raibaud; T Baltz; H Eisen
Journal:  EMBO J       Date:  1986-05       Impact factor: 11.598

10.  Telomere interactions may condition the programming of antigen expression in Trypanosoma brucei.

Authors:  A Van der Werf; S Van Assel; D Aerts; M Steinert; E Pays
Journal:  EMBO J       Date:  1990-04       Impact factor: 11.598

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