Cargando…
Phototaxis of the Unicellular Red Alga Cyanidioschyzon merolae Is Mediated by Novel Actin-Driven Tentacles
Phototaxis, which is the ability to move towards or away from a light source autonomously, is a common mechanism of unicellular algae. It evolved multiple times independently in different plant lineages. As of yet, algal phototaxis has been linked mainly to the presence of cilia, the only known loco...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503314/ https://www.ncbi.nlm.nih.gov/pubmed/32867346 http://dx.doi.org/10.3390/ijms21176209 |
_version_ | 1783584365218889728 |
---|---|
author | Maschmann, Sascha Ruban, Karin Wientapper, Johanna Walter, Wilhelm J. |
author_facet | Maschmann, Sascha Ruban, Karin Wientapper, Johanna Walter, Wilhelm J. |
author_sort | Maschmann, Sascha |
collection | PubMed |
description | Phototaxis, which is the ability to move towards or away from a light source autonomously, is a common mechanism of unicellular algae. It evolved multiple times independently in different plant lineages. As of yet, algal phototaxis has been linked mainly to the presence of cilia, the only known locomotive organelle in unicellular algae. Red algae (Rhodophyta), however, lack cilia in all stages of their life cycle. Remarkably, multiple unicellular red algae like the extremophile Cyanidioschyzon merolae (C. merolae) can move towards light. Remarkably, it has remained unclear how C. merolae achieves movement, and the presence of a completely new mechanism has been suggested. Here we show that the basis of this movement are novel retractable projections, termed tentacles due to their distinct morphology. These tentacles could be reproducibly induced within 20 min by increasing the salt concentration of the culture medium. Electron microscopy revealed filamentous structures inside the tentacles that we identified to be actin filaments. This is surprising as C. merolae’s single actin gene was previously published to not be expressed. Based on our findings, we propose a model for C. merolae’s actin-driven but myosin-independent motility. To our knowledge, the described tentacles represent a novel motility mechanism. |
format | Online Article Text |
id | pubmed-7503314 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75033142020-09-23 Phototaxis of the Unicellular Red Alga Cyanidioschyzon merolae Is Mediated by Novel Actin-Driven Tentacles Maschmann, Sascha Ruban, Karin Wientapper, Johanna Walter, Wilhelm J. Int J Mol Sci Article Phototaxis, which is the ability to move towards or away from a light source autonomously, is a common mechanism of unicellular algae. It evolved multiple times independently in different plant lineages. As of yet, algal phototaxis has been linked mainly to the presence of cilia, the only known locomotive organelle in unicellular algae. Red algae (Rhodophyta), however, lack cilia in all stages of their life cycle. Remarkably, multiple unicellular red algae like the extremophile Cyanidioschyzon merolae (C. merolae) can move towards light. Remarkably, it has remained unclear how C. merolae achieves movement, and the presence of a completely new mechanism has been suggested. Here we show that the basis of this movement are novel retractable projections, termed tentacles due to their distinct morphology. These tentacles could be reproducibly induced within 20 min by increasing the salt concentration of the culture medium. Electron microscopy revealed filamentous structures inside the tentacles that we identified to be actin filaments. This is surprising as C. merolae’s single actin gene was previously published to not be expressed. Based on our findings, we propose a model for C. merolae’s actin-driven but myosin-independent motility. To our knowledge, the described tentacles represent a novel motility mechanism. MDPI 2020-08-27 /pmc/articles/PMC7503314/ /pubmed/32867346 http://dx.doi.org/10.3390/ijms21176209 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Maschmann, Sascha Ruban, Karin Wientapper, Johanna Walter, Wilhelm J. Phototaxis of the Unicellular Red Alga Cyanidioschyzon merolae Is Mediated by Novel Actin-Driven Tentacles |
title | Phototaxis of the Unicellular Red Alga Cyanidioschyzon merolae Is Mediated by Novel Actin-Driven Tentacles |
title_full | Phototaxis of the Unicellular Red Alga Cyanidioschyzon merolae Is Mediated by Novel Actin-Driven Tentacles |
title_fullStr | Phototaxis of the Unicellular Red Alga Cyanidioschyzon merolae Is Mediated by Novel Actin-Driven Tentacles |
title_full_unstemmed | Phototaxis of the Unicellular Red Alga Cyanidioschyzon merolae Is Mediated by Novel Actin-Driven Tentacles |
title_short | Phototaxis of the Unicellular Red Alga Cyanidioschyzon merolae Is Mediated by Novel Actin-Driven Tentacles |
title_sort | phototaxis of the unicellular red alga cyanidioschyzon merolae is mediated by novel actin-driven tentacles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503314/ https://www.ncbi.nlm.nih.gov/pubmed/32867346 http://dx.doi.org/10.3390/ijms21176209 |
work_keys_str_mv | AT maschmannsascha phototaxisoftheunicellularredalgacyanidioschyzonmerolaeismediatedbynovelactindrivententacles AT rubankarin phototaxisoftheunicellularredalgacyanidioschyzonmerolaeismediatedbynovelactindrivententacles AT wientapperjohanna phototaxisoftheunicellularredalgacyanidioschyzonmerolaeismediatedbynovelactindrivententacles AT walterwilhelmj phototaxisoftheunicellularredalgacyanidioschyzonmerolaeismediatedbynovelactindrivententacles |