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The complete nucleotide sequence of chromosome 3 of Plasmodium falciparum.
Authors:S Bowman  D Lawson  D Basham  D Brown  T Chillingworth  C M Churcher  A Craig  R M Davies  K Devlin  T Feltwell  S Gentles  R Gwilliam  N Hamlin  D Harris  S Holroyd  T Hornsby  P Horrocks  K Jagels  B Jassal  S Kyes  J McLean  S Moule  K Mungall  L Murphy  K Oliver  M A Quail  M A Rajandream  S Rutter  J Skelton  R Squares  S Squares  J E Sulston  S Whitehead  J R Woodward  C Newbold  B G Barrell
Institution:Pathogen Sequencing Unit, Sanger Centre, Wellcome Trust Genome Campus, Hinxton, UK. sharen@sanger.ac.uk
Abstract:Analysis of Plasmodium falciparum chromosome 3, and comparison with chromosome 2, highlights novel features of chromosome organization and gene structure. The sub-telomeric regions of chromosome 3 show a conserved order of features, including repetitive DNA sequences, members of multigene families involved in pathogenesis and antigenic variation, a number of conserved pseudogenes, and several genes of unknown function. A putative centromere has been identified that has a core region of about 2 kilobases with an extremely high (adenine + thymidine) composition and arrays of tandem repeats. We have predicted 215 protein-coding genes and two transfer RNA genes in the 1,060,106-base-pair chromosome sequence. The predicted protein-coding genes can be divided into three main classes: 52.6% are not spliced, 45.1% have a large exon with short additional 5' or 3' exons, and 2.3% have a multiple exon structure more typical of higher eukaryotes.
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