The malaria genome sequencing project: Complete sequence of Plasmodium falciparum chromosome 2

M. J. Gardner, H. Tettelin, D. J. Carucci, L. M. Cummings, H. O. Smith, C. M. Fraser, J. C. Venter, S. L. Hoffman

Research output: Contribution to journalArticlepeer-review

Abstract

An international consortium has been formed to sequence the entire genome of the human malaria parasite Plasmodium falciparum We sequenced chromosome 2 of clone 3D7 using a shotgun sequencing strategy. Chromosome 2 is 947 kb in length, has a base composition of 80.2% A+T, and contains 210 predicted genes In comparison to the Saccharomyces cerevisiae genome, chromosome 2 has a lower gene density, a greater proportion of genes containing introns, and nearly twice as many proteins containing predicted non-globular domains. A group of putative surface proteins was identified, rifins, which are encoded by a gene family comprising up to 7% of the protein-encoding genes in the genome. The rifins exhibit considerable sequence diversity and may play an important role in antigenic variation. Sixteen genes encoded on chromosome 2 showed signs of a plastid or mitochondrial origin, including several genes involved in fatty acid biosynthesis. Completion of the chromosome 2 sequence demonstrated that the A+T-rich genome of P. falciparum can be sequenced by the shotgun approach. Within 2-3 years, the sequence of almost all P falciparum genes will have been determined, paving the way for genetic, biochemical, and immunological research aimed at developing new drugs and vaccines against malaria.

Original languageEnglish (US)
Pages (from-to)69-75
Number of pages7
JournalParassitologia
Volume41
Issue number1-3
StatePublished - Sep 1999
Externally publishedYes

Keywords

  • Chromosome 2
  • Genomics
  • Malaria
  • Malaria genome sequencing project
  • Plasmodium falciparum
  • Rifins

ASJC Scopus subject areas

  • Parasitology

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