It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
Multinuclearity is a widespread phenomenon across the living world, yet how it is achieved, and the potential related advantages, are not systematically understood. In this study, we investigate multinuclearity in amoebae. We observe that non-adherent amoebae are giant multinucleate cells compared to adherent ones. The cells solve their multinuclearity by a stretchy cytokinesis process with cytosolic bridge formation when adherence resumes. After initial adhesion to a new substrate, the progeny of the multinucleate cells is more numerous than the sibling cells generated from uninucleate amoebae. Hence, multinucleate amoebae show an advantage for population growth when the number of cells is quantified over time. Multiple nuclei per cell are observed in different amoeba species, and the lack of adhesion induces multinuclearity in diverse protists such as Acanthamoeba castellanii, Vermamoeba vermiformis, Naegleria gruberi and Hartmannella rhysodes. In this study, we observe that agitation induces a cytokinesis delay, which promotes multinuclearity. Hence, we propose the hypothesis that multinuclearity represents a physiological adaptation under non-adherent conditions that can lead to biologically relevant advantages.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details
1 URBE, University of Namur, Laboratory of Evolutionary Genetics and Ecology, Namur, Belgium (GRID:grid.6520.1) (ISNI:0000 0001 2242 8479)
2 Université de Poitiers, UMR CNRS 7267, Laboratoire Ecologie et Biologie des Interactions, Equipe Microbiologie de L’Eau, Poitiers, France (GRID:grid.11166.31) (ISNI:0000 0001 2160 6368)
3 URBE, University of Namur, Laboratory of Evolutionary Genetics and Ecology, Namur, Belgium (GRID:grid.6520.1) (ISNI:0000 0001 2242 8479); NARILIS, University of Namur (UNamur), Research Unit in the Biology of Microorganisms (URBM), Namur, Belgium (GRID:grid.6520.1) (ISNI:0000 0001 2242 8479); Vrije Universiteit Brussel (VUB), Microbial Resistance and Drug Discovery, Center for Structural Biology (CSB), Flanders Institute for Biotechnology (VIB), Brussels, Belgium (GRID:grid.8767.e) (ISNI:0000 0001 2290 8069); Vrije Universiteit Brussel (VUB), Structural Biology Brussels, Brussels, Belgium (GRID:grid.8767.e) (ISNI:0000 0001 2290 8069)