The sequence and analysis of Trypanosoma brucei chromosome II

被引:51
作者
El-Sayed, NMA
Ghedin, E
Song, JM
MacLeod, A
Bringaud, F
Larkin, C
Wanless, D
Peterson, J
Hou, LH
Taylor, S
Tweedie, A
Biteau, N
Khalak, HG
Lin, XY
Mason, T
Hannick, L
Caler, E
Blandin, G
Bartholomeu, D
Simpson, AJ
Kaul, S
Zhao, H
Pai, G
Van Aken, S
Utterback, T
Haas, B
Koo, HL
Umayam, L
Suh, B
Gerrard, C
Leech, V
Qi, R
Zhou, SG
Schwartz, D
Feldblyum, T
Salzberg, S
Tait, A
Turner, CMR
Ullu, E
White, O
Melville, S
Adams, MD
Fraser, CM
Donelson, JE
机构
[1] Inst Genom Res, Rockville, MD 20850 USA
[2] George Washington Univ, Dept Microbiol & Trop Med, Washington, DC 20052 USA
[3] Univ Glasgow, Wellcome Ctr Mol Parasitol, Glasgow G11 6NU, Lanark, Scotland
[4] Univ Bordeaux 2, CNRS, UMR5016, Mol Parasitol Lab, F-33076 Bordeaux, France
[5] Univ Glasgow, Inst Biol & Life Sci, Div Infect & Immun, Glasgow G12 8QQ, Lanark, Scotland
[6] Univ Cambridge, Dept Pathol, Cambridge CB2 1QP, England
[7] Univ Wisconsin, Dept Genet, Madison, WI 53706 USA
[8] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
[9] Yale Univ, Dept Med, New Haven, CT 06520 USA
[10] Yale Univ, Dept Cell Biol, New Haven, CT 06520 USA
[11] Univ Iowa, Dept Biochem, Iowa City, IA 52242 USA
基金
英国惠康基金; 美国国家卫生研究院;
关键词
D O I
10.1093/nar/gkg673
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report here the sequence of chromosome II from Trypanosoma brucei, the causative agent of African sleeping sickness. The 1.2-Mb pairs encode about 470 predicted genes organised in 17 directional clusters on either strand, the largest cluster of which has 92 genes lined up over a 284-kb region. An analysis of the GC skew reveals strand compositional asymmetries that coincide with the distribution of protein-coding genes, suggesting these asymmetries may be the result of transcription-coupled repair on coding versus non-coding strand. A 5-cM genetic map of the chromosome reveals recombinational 'hot' and 'cold' regions, the latter of which is predicted to include the putative centromere. One end of the chromosome consists of a 250-kb region almost exclusively composed of RHS (pseudo)genes that belong to a newly characterised multigene family containing a hot spot of insertion for retroelements. Interspersed with the RHS genes are a few copies of truncated RNA polymerase pseudogenes as well as expression site associated (pseudo)genes (ESAGs) 3 and 4, and 76 bp repeats. These features are reminiscent of a vestigial variant surface glycoprotein (VSG) gene expression site. The other end of the chromosome contains a 30-kb array of VSG genes, the majority of which are pseudogenes, suggesting that this region may be a site for modular de novo construction of VSG gene diversity during transposition/gene conversion events.
引用
收藏
页码:4856 / 4863
页数:8
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