Author
Listed:
- Evelien M. Bunnik
(The University of Texas Health Science Center at San Antonio
University of California Riverside)
- Kate B. Cook
(University of Washington)
- Nelle Varoquaux
(University of California
Berkeley Institute for Data Science
MINES ParisTech, PSL Research University, CBIO-Centre for Computational Biology
Institut Curie)
- Gayani Batugedara
(University of California Riverside)
- Jacques Prudhomme
(University of California Riverside)
- Anthony Cort
(University of California Riverside)
- Lirong Shi
(Johns Hopkins Bloomberg School of Public Health)
- Chiara Andolina
(University of Oxford, Old Road campus
Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Mae Sot)
- Leila S. Ross
(Columbia University Medical Center)
- Declan Brady
(Queens Medical Centre, University of Nottingham)
- David A. Fidock
(Columbia University Medical Center
Columbia University)
- Francois Nosten
(University of Oxford, Old Road campus
Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Mae Sot)
- Rita Tewari
(Queens Medical Centre, University of Nottingham)
- Photini Sinnis
(Johns Hopkins Bloomberg School of Public Health)
- Ferhat Ay
(La Jolla Institute for Allergy & Immunology)
- Jean-Philippe Vert
(MINES ParisTech, PSL Research University, CBIO-Centre for Computational Biology
Institut Curie
U900, INSERM
École normale supérieure, CNRS, PSL Research University)
- William Stafford Noble
(University of Washington
University of Washington)
- Karine G. Le Roch
(University of California Riverside)
Abstract
The development of malaria parasites throughout their various life cycle stages is coordinated by changes in gene expression. We previously showed that the three-dimensional organization of the Plasmodium falciparum genome is strongly associated with gene expression during its replication cycle inside red blood cells. Here, we analyze genome organization in the P. falciparum and P. vivax transmission stages. Major changes occur in the localization and interactions of genes involved in pathogenesis and immune evasion, host cell invasion, sexual differentiation, and master regulation of gene expression. Furthermore, we observe reorganization of subtelomeric heterochromatin around genes involved in host cell remodeling. Depletion of heterochromatin protein 1 (PfHP1) resulted in loss of interactions between virulence genes, confirming that PfHP1 is essential for maintenance of the repressive center. Our results suggest that the three-dimensional genome structure of human malaria parasites is strongly connected with transcriptional activity of specific gene families throughout the life cycle.
Suggested Citation
Evelien M. Bunnik & Kate B. Cook & Nelle Varoquaux & Gayani Batugedara & Jacques Prudhomme & Anthony Cort & Lirong Shi & Chiara Andolina & Leila S. Ross & Declan Brady & David A. Fidock & Francois Nos, 2018.
"Changes in genome organization of parasite-specific gene families during the Plasmodium transmission stages,"
Nature Communications, Nature, vol. 9(1), pages 1-15, December.
Handle:
RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-04295-5
DOI: 10.1038/s41467-018-04295-5
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