The DNA sequence of chromosome I of an African trypanosome:: gene content, chromosome organisation, recombination and polymorphism

被引:53
作者
Hall, N
Berriman, M
Lennard, NJ
Harris, BR
Hertz-Fowler, C
Bart-Delabesse, EN
Gerrard, CS
Atkin, RJ
Barron, AJ
Bowman, S
Bray-Allen, SP
Bringaud, F
Clark, LN
Corton, CH
Cronin, A
Davies, R
Doggett, J
Fraser, A
Grüter, E
Hall, S
Harper, AD
Kay, MP
Leech, V
Mayes, R
Price, C
Quail, MA
Rabbinowitsch, E
Reitter, C
Rutherford, K
Sasse, J
Sharp, S
Shownkeen, R
MacLeod, A
Taylor, S
Tweedie, A
Turner, CMR
Tait, A
Gull, K
Barrell, B
Melville, SE
机构
[1] Wellcome Trust Sanger Inst, Hinxton CB10 1SA, England
[2] Univ Cambridge, Dept Pathol, Cambridge CB2 1QP, England
[3] Univ Bordeaux 2, F-33076 Bordeaux, France
[4] Univ Glasgow, Wellcome Ctr Mol Parasitol, Glasgow G11 6NU, Lanark, Scotland
[5] Inst Biol & Life Sci, Div Infect & Immunol, Glasgow G12 8QQ, Lanark, Scotland
[6] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
基金
英国惠康基金;
关键词
D O I
10.1093/nar/gkg674
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
The African trypanosome, Trypanosoma brucei, causes sleeping sickness in humans in sub-Saharan Africa. Here we report the sequence and analysis of the 1.1 Mb chromosome I, which encodes approximately 400 predicted genes organised into directional clusters, of which more than 100 are located in the largest cluster of 250 kb. A 160-kb region consists primarily of three gene families of unknown function, one of which contains a hotspot for retroelement insertion. We also identify five novel gene families. Indeed, almost 20% of predicted genes are members of families. In some cases, tandemly arrayed genes are 99-100% identical, suggesting an active process of amplification and gene conversion. One end of the chromosome consists of a putative bloodstream-form variant surface glycoprotein (VSG) gene expression site that appears truncated and degenerate. The other chromosome end carries VSG and expression site-associated genes and pseudogenes over 50 kb of subtelomeric sequence where, unusually, the telomere-proximal VSG gene is oriented away from the telomere. Our analysis includes the cataloguing of minor genetic variations between the chromosome I homologues and an estimate of crossing-over frequency during genetic exchange. Genetic polymorphisms are exceptionally rare in sequences located within and around the strand-switches between several gene clusters.
引用
收藏
页码:4864 / 4873
页数:10
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