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The genome of the African trypanosome Trypanosoma brucei

Authors :
David W. Johnson
Barclay G. Barrell
Sharon Moule
Luke J. Tallon
Ian Goodhead
Lihua Hou
Jeremy Peterson
Danielle Walker
David M. A. Martin
Sara E. Melville
Kristine Jones
Martin Aslett
Appolinaire Djikeng
Neil Hall
Inna Cherevach
Hean Koo
Ester Rabbinowitsch
Steven L. Salzberg
Sarah Sharp
Mark Raymond Adams
Claire Arrowsmith
Andrew Barron
Elisabetta Ullu
Rebecca Atkin
Mark Simmonds
Al Ivens
John E. Donelson
Elodie Ghedin
P. Mooney
Adrian Tivey
Tamara Feldblyum
Audrey Fraser
Natasha Larke
Keith Gull
Jonathon Doggett
Doug Ormond
Jennifer R. Wortman
Claire M. Fraser
Carol Churcher
Mark Carrington
Chris P Reitter
Anjana J. Simpson
Joshua Shallom
Louise Clark
Brian J. Haas
Arnaud Kerhornou
Andrew Tait
Matthew Berriman
Mandy Sanders
Halina Norbertczak
Justin Johnson
Sally Whitehead
Jessica B. Hostetler
Scott M. Landfear
Frédéric Bringaud
Barbara Harris
Ann Cronin
J. David Barry
Fred R. Opperdoes
U. Cecilia M. Alsmark
Brian White
Craig Corton
John Woodward
Najib M. El-Sayed
Alexandra Line
Elisabet Caler
Annette MacLeod
Heidi Hauser
T. Martin Embley
Marie-Adèle Rajandream
Daniella Castanheira Bartholomeu
Mark C. Field
Angela Lord
Linda Hannick
C. Michael R. Turner
Gareth W. Morgan
Hubert Renauld
Bill Wickstead
Christiane Hertz-Fowler
Gaëlle Blandin
Shiliang Wang
Christopher S. Peacock
Tracey-Jane Chillingworth
Michael A. Quail
Karen Mungall
Robert L. Davies
Vanessa Leech
Alan H. Fairlamb
Susan Van Aken
Nicola Lennard
N. Hamlin
Ulrike Böhme
Karen Brooks
Owen White
Christopher Larkin
Lucio Marcello
Zahra Hance
David Harper
David Wanless
Grace Pai
Kay Jagels
Seth Schobel
Publication Year :
2016

Abstract

African trypanosomes cause human sleeping sickness and livestock trypanosomiasis in sub-Saharan Africa. We present the sequence and analysis of the 11 megabase-sized chromosomes of Trypanosoma brucei . The 26-megabase genome contains 9068 predicted genes, including ∼900 pseudogenes and ∼1700 T. brucei –specific genes. Large subtelomeric arrays contain an archive of 806 variant surface glycoprotein (VSG) genes used by the parasite to evade the mammalian immune system. Most VSG genes are pseudogenes, which may be used to generate expressed mosaic genes by ectopic recombination. Comparisons of the cytoskeleton and endocytic trafficking systems with those of humans and other eukaryotic organisms reveal major differences. A comparison of metabolic pathways encoded by the genomes of T. brucei, T. cruzi , and Leishmania major reveals the least overall metabolic capability in T. brucei and the greatest in L. major . Horizontal transfer of genes of bacterial origin has contributed to some of the metabolic differences in these parasites, and a number of novel potential drug targets have been identified.

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....3750ef339c57c8ea7b18444005230de3