The genetic map and comparative analysis with the physical map of Trypanosoma brucei

被引:49
作者
MacLeod, A
Tweedie, A
McLellan, S
Taylor, S
Hall, N
Berriman, M
El-Sayed, NM
Hope, M
Turner, CMR
Tait, A
机构
[1] Univ Glasgow, Wellcome Ctr Mol Parasitol, Glasgow G11 6NU, Lanark, Scotland
[2] Univ Glasgow, Inst Biomed & Life Sci, Div Infect & Immun, Glasgow G12 8QQ, Lanark, Scotland
[3] Wellcome Trust Sanger Inst, Hinxton CB10 1SA, England
[4] Inst Genom Res, Rockville, MD 20850 USA
基金
英国惠康基金;
关键词
Boolean function; Horn function; prime implicant; P-complete;
D O I
10.1093/nar/gki980
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
Trypanosoma brucei is the causative agent of African sleeping sickness in humans and contributes to the debilitating disease 'Nagana' in cattle. To date we know little about the genes that determine drug resistance, host specificity, pathogenesis and virulence in these parasites. The availability of the complete genome sequence and the ability of the parasite to undergo genetic exchange have allowed genetic investigations into this parasite and here we report the first genetic map of T.brucei for the genome reference stock TREU 927, comprising of 182 markers and 11 major linkage groups, that correspond to the 11 previously identified chromosomes. The genetic map provides 90% probability of a marker being 11 cM from any given locus. Its comparison to the available physical map has revealed the average physical size of a recombination unit to be 15.6 Kb/cM. The genetic map coupled with the genome sequence and the ability to undertake crosses presents a new approach to identifying genes relevant to the disease and its prevention in this important pathogen through forward genetic analysis and positional cloning.
引用
收藏
页码:6688 / 6693
页数:6
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