AJTMH HINARI
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am. J. Trop. Med. Hyg., 67(3), 2002, pp. 233-243
Copyright © 2002 by The American Society of Tropical Medicine and Hygiene

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Le Roch, K.
Right arrow Articles by Winzeler, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Le Roch, K.
Right arrow Articles by Winzeler, E.
Related Collections
Right arrow Malaria
American Journal of Tropical Medicine and Hygiene, Vol 67, Issue 3, 233-243
Copyright © 2002 by American Society of Tropical Medicine and Hygiene

Research Articles


Monitoring the chromosome 2 intraerythrocytic transcriptome of Plasmodium falciparum using oligonucleotide arrays

KG Le Roch, Y Zhou, S Batalov, and EA Winzeler

To test the feasibility of using short oligonucleotide probes to monitor transcript levels in Plasmodium falciparum, a microarray was manufactured containing 4,167 (25 base single-stranded) probes derived from the predicted coding region of P. falciparum chromosome 2. RNA samples from three asexual stages (rings, trophozoites, and schizonts) were labeled and hybridized to the arrays. These results were reproducible, and transcripts were detected for 69% of the 210 genes on chromosome 2. In addition, of the 145 expressed genes, 1/3 appeared to be differentially transcribed during the asexual cycle. Some regions of the chromosome appeared to be transcriptionally silent. Results were confirmed by Northern blot analysis and by quantitative reverse transcriptase-polymerase chain reaction. These data validate the use of relatively short 25-mers for monitoring the expression of a genome that is 82% AT rich.


This article has been cited by other articles:


Home page
Infect. Immun.Home page
J. E. McCoubrie, S. K. Miller, T. Sargeant, R. T. Good, A. N. Hodder, T. P. Speed, T. F. de Koning-Ward, and B. S. Crabb
Evidence for a Common Role for the Serine-Type Plasmodium falciparum Serine Repeat Antigen Proteases: Implications for Vaccine and Drug Design
Infect. Immun., December 1, 2007; 75(12): 5565 - 5574.
[Abstract] [Full Text] [PDF]


Home page
BioinformaticsHome page
Y. Zhou, J. A. Young, A. Santrosyan, K. Chen, S. F. Yan, and E. A. Winzeler
In silico gene function prediction using ontology-based pattern identification
Bioinformatics, April 1, 2005; 21(7): 1237 - 1245.
[Abstract] [Full Text] [PDF]


Home page
Genome ResHome page
K. G. Le Roch, J. R. Johnson, L. Florens, Y. Zhou, A. Santrosyan, M. Grainger, S. F. Yan, K. C. Williamson, A. A. Holder, D. J. Carucci, et al.
Global analysis of transcript and protein levels across the Plasmodium falciparum life cycle
Genome Res., November 1, 2004; 14(11): 2308 - 2318.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
K. G. Le Roch, Y. Zhou, P. L. Blair, M. Grainger, J. K. Moch, J. D. Haynes, P. De la Vega, A. A. Holder, S. Batalov, D. J. Carucci, et al.
Discovery of Gene Function by Expression Profiling of the Malaria Parasite Life Cycle
Science, September 12, 2003; 301(5639): 1503 - 1508.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2002 by the American Society of Tropical Medicine and Hygiene.