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Host-encoded ETP2 is involved in recruiting the dynamin-like protein ETP9 to the endosymbiont division site in trypanosomatid Angomonas deanei
Host-encoded ETP2 is involved in recruiting the dynamin-like protein ETP9 to the endosymbiont division site in trypanosomatid Angomonas deanei
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Host-encoded ETP2 is involved in recruiting the dynamin-like protein ETP9 to the endosymbiont division site in trypanosomatid Angomonas deanei
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Host-encoded ETP2 is involved in recruiting the dynamin-like protein ETP9 to the endosymbiont division site in trypanosomatid Angomonas deanei
Host-encoded ETP2 is involved in recruiting the dynamin-like protein ETP9 to the endosymbiont division site in trypanosomatid Angomonas deanei

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Host-encoded ETP2 is involved in recruiting the dynamin-like protein ETP9 to the endosymbiont division site in trypanosomatid Angomonas deanei
Host-encoded ETP2 is involved in recruiting the dynamin-like protein ETP9 to the endosymbiont division site in trypanosomatid Angomonas deanei
Journal Article

Host-encoded ETP2 is involved in recruiting the dynamin-like protein ETP9 to the endosymbiont division site in trypanosomatid Angomonas deanei

2025
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Overview
The ancient uptake and transformation of free-living bacteria into eukaryotic organelles involved extensive structural, physiological, and genetic changes. More recently established endosymbioses offer a unique opportunity to observe intermediate stages in the complex process by which a prokaryote becomes genetically integrated into a eukaryotic cell. Hence, studying the molecular mechanisms that govern host-endosymbiont interactions holds the potential for uncovering the scenarios and molecular processes behind organelle formation. The trypanosomatid Angomonas deanei has been recently reported to manifest nuclear control over its endosymbiont’s division. In this study, we identified and characterized a new nucleus-encoded component of the endosymbiont division machinery. This study further supports that a novel intermediate between endosymbiont and organelle evolved in A. deanei and provides new leverage to entangle the evolution of its fascinating nucleus-controlled endosymbiont division machinery.