Heterochromatin Protein 1 Secures Survival and Transmission of Malaria Parasites

Clonally variant expression of surface antigens allows the malaria parasite Plasmodium falciparum to evade immune recognition during blood stage infection and secure malaria transmission. We demonstrate that heterochromatin protein 1 (HP1), an evolutionary conserved regulator of heritable gene silen...

Full description

Saved in:
Bibliographic Details
Main Authors: Brancucci, Nicolas M.B., Bertschi, Nicole L., Zhu, Lei, Niederwieser, Igor, Chin, Wai Hoe, Wampfler, Rahel, Freymond, Céline, Rottmann, Matthias, Felger, Ingrid, Bozdech, Zbynek, Voss, Till S.
Other Authors: School of Biological Sciences
Format: Article
Language:English
Published: 2016
Subjects:
Online Access:https://hdl.handle.net/10356/82524
http://hdl.handle.net/10220/40061
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-82524
record_format dspace
spelling sg-ntu-dr.10356-825242020-03-07T12:18:05Z Heterochromatin Protein 1 Secures Survival and Transmission of Malaria Parasites Brancucci, Nicolas M.B. Bertschi, Nicole L. Zhu, Lei Niederwieser, Igor Chin, Wai Hoe Wampfler, Rahel Freymond, Céline Rottmann, Matthias Felger, Ingrid Bozdech, Zbynek Voss, Till S. School of Biological Sciences Biological Sciences Clonally variant expression of surface antigens allows the malaria parasite Plasmodium falciparum to evade immune recognition during blood stage infection and secure malaria transmission. We demonstrate that heterochromatin protein 1 (HP1), an evolutionary conserved regulator of heritable gene silencing, controls expression of numerous P. falciparum virulence genes as well as differentiation into the sexual forms that transmit to mosquitoes. Conditional depletion of P. falciparum HP1 (PfHP1) prevents mitotic proliferation of blood stage parasites and disrupts mutually exclusive expression and antigenic variation of the major virulence factor PfEMP1. Additionally, PfHP1-dependent regulation of PfAP2-G, a transcription factor required for gametocyte conversion, controls the switch from asexual proliferation to sexual differentiation, providing insight into the epigenetic mechanisms underlying gametocyte commitment. These findings show that PfHP1 is centrally involved in clonally variant gene expression and sexual differentiation in P. falciparum and have major implications for developing antidisease and transmission-blocking interventions against malaria. NMRC (Natl Medical Research Council, S’pore) 2016-02-23T06:47:36Z 2019-12-06T14:57:18Z 2016-02-23T06:47:36Z 2019-12-06T14:57:18Z 2014 Journal Article Brancucci, N., Bertschi, N., Zhu, L., Niederwieser, I., Chin, W., Wampfler, R., Freymond, C., Rottmann, M., Felger, I., Bozdech, Z.,& Voss, T. (2014). Heterochromatin Protein 1 Secures Survival and Transmission of Malaria Parasites. Cell Host & Microbe, 16(2), 165-176. 1931-3128 https://hdl.handle.net/10356/82524 http://hdl.handle.net/10220/40061 10.1016/j.chom.2014.07.004 en Cell Host & Microbe © 2014 Elsevier Inc.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic Biological Sciences
spellingShingle Biological Sciences
Brancucci, Nicolas M.B.
Bertschi, Nicole L.
Zhu, Lei
Niederwieser, Igor
Chin, Wai Hoe
Wampfler, Rahel
Freymond, Céline
Rottmann, Matthias
Felger, Ingrid
Bozdech, Zbynek
Voss, Till S.
Heterochromatin Protein 1 Secures Survival and Transmission of Malaria Parasites
description Clonally variant expression of surface antigens allows the malaria parasite Plasmodium falciparum to evade immune recognition during blood stage infection and secure malaria transmission. We demonstrate that heterochromatin protein 1 (HP1), an evolutionary conserved regulator of heritable gene silencing, controls expression of numerous P. falciparum virulence genes as well as differentiation into the sexual forms that transmit to mosquitoes. Conditional depletion of P. falciparum HP1 (PfHP1) prevents mitotic proliferation of blood stage parasites and disrupts mutually exclusive expression and antigenic variation of the major virulence factor PfEMP1. Additionally, PfHP1-dependent regulation of PfAP2-G, a transcription factor required for gametocyte conversion, controls the switch from asexual proliferation to sexual differentiation, providing insight into the epigenetic mechanisms underlying gametocyte commitment. These findings show that PfHP1 is centrally involved in clonally variant gene expression and sexual differentiation in P. falciparum and have major implications for developing antidisease and transmission-blocking interventions against malaria.
author2 School of Biological Sciences
author_facet School of Biological Sciences
Brancucci, Nicolas M.B.
Bertschi, Nicole L.
Zhu, Lei
Niederwieser, Igor
Chin, Wai Hoe
Wampfler, Rahel
Freymond, Céline
Rottmann, Matthias
Felger, Ingrid
Bozdech, Zbynek
Voss, Till S.
format Article
author Brancucci, Nicolas M.B.
Bertschi, Nicole L.
Zhu, Lei
Niederwieser, Igor
Chin, Wai Hoe
Wampfler, Rahel
Freymond, Céline
Rottmann, Matthias
Felger, Ingrid
Bozdech, Zbynek
Voss, Till S.
author_sort Brancucci, Nicolas M.B.
title Heterochromatin Protein 1 Secures Survival and Transmission of Malaria Parasites
title_short Heterochromatin Protein 1 Secures Survival and Transmission of Malaria Parasites
title_full Heterochromatin Protein 1 Secures Survival and Transmission of Malaria Parasites
title_fullStr Heterochromatin Protein 1 Secures Survival and Transmission of Malaria Parasites
title_full_unstemmed Heterochromatin Protein 1 Secures Survival and Transmission of Malaria Parasites
title_sort heterochromatin protein 1 secures survival and transmission of malaria parasites
publishDate 2016
url https://hdl.handle.net/10356/82524
http://hdl.handle.net/10220/40061
_version_ 1681040278265266176