Skip Navigation

This Article
Right arrow Print PDF (4261K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Matthews, K. R.
Right arrow Articles by Barry, J.D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Matthews, K. R.
Right arrow Articles by Barry, J.D.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1990, Vol. 18, No. 24 7219-7227
© 1990


Articles

Duplicative activation mechanisms of two trypanosome telomeric VSG genes with structurally simple 5' flanks

Keith R. Matthews+, Paul G. Shiels§, Sheila V. Graham, Catriona Cowan and J.David Barry*

Institute of Genetics and Wellcome Unit of Molecular Parasitology, Glasgow University Church street, Glasgow G11 5JS, UK

*To whom correspondence should be addressed

Received October 23, 1990. Revised November 26, 1990. Accepted November 26, 1990.

In the mammalian bloodstream, African trypanosomes express variant surface glycoprotein (VSG) genes from a family of long and complex telomeric expression sites. VSG switching generally occurs by the duplication of different VSG genes into these sites by gene conversion involving a series of 70 base pair (70bp) repeats in the 5' flank. In contrast, when VSG is first synthesised by trypanosomes in the tsetse fly at the metacyclic stage, a separate set of telomeric expression sites is activated. These latter telomeres appear not to act as recipients in gene conversion. We have found that the structure of two such expression sites is simple, with very short 70bp repeat regions and very little other sequence in common with bloodstream expression sites. However, the two telomeres readily act as donors in VSG gene conversion in the bloodstream and we show for one a consistent association of the conversion 5' end point with the short 70bp repeat region. These findings help explain why a very predictable set of VSGs is expressed in the tsetse fly and have implications for VSG gene conversion mechanisms.


Present address: +Department of Internal Medicine, Yale MacArthur Center for Molecular Parasitology, Yale University School of Medicine, New Haven, CN, USA

Present address: §Division of Molecular Biology, The Netherlands Cancer Institute (Antoni van Leeuwenhoek Huis) Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Nucleic Acids ResHome page
D. J. LaCount, N. M. El-Sayed, S. Kaul, D. Wanless, C. M. R. Turner, and J. E. Donelson
Analysis of a donor gene region for a variant surface glycoprotein and its expression site in African trypanosomes
Nucleic Acids Res., May 15, 2001; 29(10): 2012 - 2019.
[Abstract] [Full Text] [PDF]


Home page
Infect. Immun.Home page
J. R. Stringer and S. P. Keely
Genetics of Surface Antigen Expression in Pneumocystis carinii
Infect. Immun., February 1, 2001; 69(2): 627 - 639.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
N. P. Robinson, N. Burman, S. E. Melville, and J. D. Barry
Predominance of Duplicative VSG Gene Conversion in Antigenic Variation in African Trypanosomes
Mol. Cell. Biol., September 1, 1999; 19(9): 5839 - 5846.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
S. V. Graham, B. Wymer, and J. D. Barry
Activity of a Trypanosome Metacyclic Variant Surface Glycoprotein Gene Promoter Is Dependent upon Life Cycle Stage and Chromosomal Context
Mol. Cell. Biol., March 1, 1998; 18(3): 1137 - 1146.
[Abstract] [Full Text]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.