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Discovery of gene function by expression profiling of the malaria parasite life cycle

Academic Article
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Overview

authors

  • Le Roch, K. G.
  • Zhou, Y. Y.
  • Blair, P. L.
  • Grainger, M.
  • Moch, J. K.
  • Haynes, J. D.
  • De la Vega, P.
  • Holder, A. A.
  • Batalov, S.
  • Carucci, D. J.
  • Winzeler, Elizabeth

publication date

  • September 2003

journal

  • Science  Journal

abstract

  • The completion of the genome sequence for Plasmodium falciparum, the species responsible for most malaria human deaths, has the potential to reveal hundreds of new drug targets and proteins involved in pathogenesis. However, only approximately 35% of the genes code for proteins with an identifiable function. The absence of routine genetic tools for studying Plasmodium parasites suggests that this number is unlikely to change quickly if conventional serial methods are used to characterize encoded proteins. Here, we use a high-density oligonucleotide array to generate expression profiles of human and mosquito stages of the malaria parasite's life cycle. Genes with highly correlated levels and temporal patterns of expression were often involved in similar functions or cellular processes.

subject areas

  • Animals
  • Anopheles
  • Cell Cycle
  • Chromosomes
  • Cluster Analysis
  • Erythrocytes
  • Gene Expression
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental
  • Genes, Protozoan
  • Humans
  • Life Cycle Stages
  • Liver
  • Malaria, Falciparum
  • Oligonucleotide Array Sequence Analysis
  • Plasmodium falciparum
  • Proteome
  • Protozoan Proteins
  • RNA, Messenger
  • RNA, Protozoan
  • Salivary Glands
  • Sporozoites
  • Transcription, Genetic
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Identity

International Standard Serial Number (ISSN)

  • 0036-8075

Digital Object Identifier (DOI)

  • 10.1126/science.1087025

PubMed ID

  • 12893887
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Additional Document Info

start page

  • 1503

end page

  • 1508

volume

  • 301

issue

  • 5639

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