Changes in genome organization of parasite-specific gene families during the Plasmodium transmission stages

Evelien M. Bunnik(University of California, Riverside), Kate B. Cook(University of Washington), Nelle Varoquaux(Berkeley College), Gayani Batugedara(University of California, Riverside), Jacques Prudhomme(University of California, Riverside), Anthony Cort(University of California, Riverside), Lirong Shi(Johns Hopkins University), Chiara Andolina(Mahidol University), Leila S. Ross(Columbia University Irving Medical Center), Declan Brady(University of Nottingham), David A. Fidock(Columbia University Irving Medical Center), François Nosten(Mahidol University), Rita Tewari(University of Nottingham), Photini Sinnis(Johns Hopkins University), Ferhat Ay(La Jolla Institute for Immunology), Jean‐Philippe Vert(Centre National de la Recherche Scientifique), William Stafford Noble(University of Washington), Karine G. Le Roch(University of California, Riverside)
Nature Communications
May 9, 2018
Cited by 137Open Access
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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.


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