Malaria remains one of the most deadly infectious diseases in the developing world. The absence of a vaccine and the development of parasite resistance to commonly used antimalarial drugs underscore the urgent need for new therapeutic approaches. The goal of this project is to generate insights into the mechanisms whereby Plas- modium falciparum, the parasite responsible for the most virulent form of malaria, regulates its genes'expression throughout its life cycle. Mechanisms controlling gene expression in the parasite are still poorly understood. Increasing evidence indicates that control of gene expression in Plasmodium occurs at multiple levels, via local protein-DNA binding events, patterns of histone modifications, local chromatin structure and nucleosome occupancy, and large-scale chromatin structure. A variety of existing genome-wide data sets, including the genomic DNA sequence as well as measurements of RNA expression levels and nucleosome occupancy, provide insight into many aspects of this regulatory machinery. However, a global picture of the structure of DNA in the nucleus of the parasite is not yet available. This project will apply a recently developed technology to map in Plasmodium all intra- and inter-chromosomal interactions at kilobase resolution throughout the parasite life cycle. These data will be used to build a dynamic three-dimensional model of the Plasmodium genome in vivo. The project will also generate a series of maps of histone modifications genome-wide. Finally, these two new data sets, along with existing data sets, will be integrated using machine learning methods to produce a predictive model of gene expression across the Plasmodium eryrthrocytic cycle. Rational drug design requires a detailed understanding of the molecular basis of disease. By providing fundamental insight into the regulatory mechanisms of the malaria parasite, this project will improve our ability to design new drugs and novel lines of defense against malaria.

Public Health Relevance

To develop effective strategies for combating malaria, we must understand the biology of Plasmodium falciparum, the parasite that causes the most lethal form of the disease. This project will use a recently developed technique to discover the spatial organization of the Plasmodium genome during the parasite infectious cycle. The resulting data will be integrated with newly generated patterns of histone modifications and will be used in combination with published genome-wide data sets to develop a computational model that will yield insights into transcriptional regulation in the human malaria parasite.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI106775-02
Application #
8675801
Study Section
Biodata Management and Analysis Study Section (BDMA)
Program Officer
Joy, Deirdre A
Project Start
2013-06-07
Project End
2017-05-31
Budget Start
2014-06-01
Budget End
2015-05-31
Support Year
2
Fiscal Year
2014
Total Cost
$454,989
Indirect Cost
$64,372
Name
University of Washington
Department
Genetics
Type
Schools of Medicine
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
Bunnik, Evelien M; Cook, Kate B; Varoquaux, Nelle et al. (2018) Changes in genome organization of parasite-specific gene families during the Plasmodium transmission stages. Nat Commun 9:1910
Lapp, S A; Geraldo, J A; Chien, J-T et al. (2018) PacBio assembly of a Plasmodium knowlesi genome sequence with Hi-C correction and manual annotation of the SICAvar gene family. Parasitology 145:71-84
Rea, Edward; Le Roch, Karine G; Tewari, Rita (2018) Sex in Plasmodium falciparum: Silence Play between GDV1 and HP1. Trends Parasitol 34:450-452
Galinski, M R; Lapp, S A; Peterson, M S et al. (2018) Plasmodium knowlesi: a superb in vivo nonhuman primate model of antigenic variation in malaria. Parasitology 145:85-100
Batugedara, Gayani; Le Roch, Karine G (2018) Unraveling the 3D genome of human malaria parasites. Semin Cell Dev Biol :
Batugedara, Gayani; Lu, Xueqing M; Bunnik, Evelien M et al. (2017) The Role of Chromatin Structure in Gene Regulation of the Human Malaria Parasite. Trends Parasitol 33:364-377
Lu, Xueqing Maggie; Batugedara, Gayani; Lee, Michael et al. (2017) Nascent RNA sequencing reveals mechanisms of gene regulation in the human malaria parasite Plasmodium falciparum. Nucleic Acids Res 45:7825-7840
Saraf, Anita; Cervantes, Serena; Bunnik, Evelien M et al. (2016) Dynamic and Combinatorial Landscape of Histone Modifications during the Intraerythrocytic Developmental Cycle of the Malaria Parasite. J Proteome Res 15:2787-801
Bunnik, Evelien M; Batugedara, Gayani; Saraf, Anita et al. (2016) The mRNA-bound proteome of the human malaria parasite Plasmodium falciparum. Genome Biol 17:147
Lu, Xueqing Maggie; Bunnik, Evelien M; Pokhriyal, Neeti et al. (2015) Analysis of nucleosome positioning landscapes enables gene discovery in the human malaria parasite Plasmodium falciparum. BMC Genomics 16:1005

Showing the most recent 10 out of 16 publications