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Genome evolution of a nonparasitic secondary heterotroph, the diatom Nitzschia putrida
Secondary loss of photosynthesis is observed across almost all plastid-bearing branches of the eukaryotic tree of life. However, genome-based insights into the transition from a phototroph into a secondary heterotroph have so far only been revealed for parasitic species. Free-living organisms can yi...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054022/ https://www.ncbi.nlm.nih.gov/pubmed/35486731 http://dx.doi.org/10.1126/sciadv.abi5075 |
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author | Kamikawa, Ryoma Mochizuki, Takako Sakamoto, Mika Tanizawa, Yasuhiro Nakayama, Takuro Onuma, Ryo Cenci, Ugo Moog, Daniel Speak, Samuel Sarkozi, Krisztina Toseland, Andrew van Oosterhout, Cock Oyama, Kaori Kato, Misako Kume, Keitaro Kayama, Motoki Azuma, Tomonori Ishii, Ken-ichiro Miyashita, Hideaki Henrissat, Bernard Lombard, Vincent Win, Joe Kamoun, Sophien Kashiyama, Yuichiro Mayama, Shigeki Miyagishima, Shin-ya Tanifuji, Goro Mock, Thomas Nakamura, Yasukazu |
author_facet | Kamikawa, Ryoma Mochizuki, Takako Sakamoto, Mika Tanizawa, Yasuhiro Nakayama, Takuro Onuma, Ryo Cenci, Ugo Moog, Daniel Speak, Samuel Sarkozi, Krisztina Toseland, Andrew van Oosterhout, Cock Oyama, Kaori Kato, Misako Kume, Keitaro Kayama, Motoki Azuma, Tomonori Ishii, Ken-ichiro Miyashita, Hideaki Henrissat, Bernard Lombard, Vincent Win, Joe Kamoun, Sophien Kashiyama, Yuichiro Mayama, Shigeki Miyagishima, Shin-ya Tanifuji, Goro Mock, Thomas Nakamura, Yasukazu |
author_sort | Kamikawa, Ryoma |
collection | PubMed |
description | Secondary loss of photosynthesis is observed across almost all plastid-bearing branches of the eukaryotic tree of life. However, genome-based insights into the transition from a phototroph into a secondary heterotroph have so far only been revealed for parasitic species. Free-living organisms can yield unique insights into the evolutionary consequence of the loss of photosynthesis, as the parasitic lifestyle requires specific adaptations to host environments. Here, we report on the diploid genome of the free-living diatom Nitzschia putrida (35 Mbp), a nonphotosynthetic osmotroph whose photosynthetic relatives contribute ca. 40% of net oceanic primary production. Comparative analyses with photosynthetic diatoms and heterotrophic algae with parasitic lifestyle revealed that a combination of gene loss, the accumulation of genes involved in organic carbon degradation, a unique secretome, and the rapid divergence of conserved gene families involved in cell wall and extracellular metabolism appear to have facilitated the lifestyle of a free-living secondary heterotroph. |
format | Online Article Text |
id | pubmed-9054022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-90540222022-05-04 Genome evolution of a nonparasitic secondary heterotroph, the diatom Nitzschia putrida Kamikawa, Ryoma Mochizuki, Takako Sakamoto, Mika Tanizawa, Yasuhiro Nakayama, Takuro Onuma, Ryo Cenci, Ugo Moog, Daniel Speak, Samuel Sarkozi, Krisztina Toseland, Andrew van Oosterhout, Cock Oyama, Kaori Kato, Misako Kume, Keitaro Kayama, Motoki Azuma, Tomonori Ishii, Ken-ichiro Miyashita, Hideaki Henrissat, Bernard Lombard, Vincent Win, Joe Kamoun, Sophien Kashiyama, Yuichiro Mayama, Shigeki Miyagishima, Shin-ya Tanifuji, Goro Mock, Thomas Nakamura, Yasukazu Sci Adv Biomedicine and Life Sciences Secondary loss of photosynthesis is observed across almost all plastid-bearing branches of the eukaryotic tree of life. However, genome-based insights into the transition from a phototroph into a secondary heterotroph have so far only been revealed for parasitic species. Free-living organisms can yield unique insights into the evolutionary consequence of the loss of photosynthesis, as the parasitic lifestyle requires specific adaptations to host environments. Here, we report on the diploid genome of the free-living diatom Nitzschia putrida (35 Mbp), a nonphotosynthetic osmotroph whose photosynthetic relatives contribute ca. 40% of net oceanic primary production. Comparative analyses with photosynthetic diatoms and heterotrophic algae with parasitic lifestyle revealed that a combination of gene loss, the accumulation of genes involved in organic carbon degradation, a unique secretome, and the rapid divergence of conserved gene families involved in cell wall and extracellular metabolism appear to have facilitated the lifestyle of a free-living secondary heterotroph. American Association for the Advancement of Science 2022-04-29 /pmc/articles/PMC9054022/ /pubmed/35486731 http://dx.doi.org/10.1126/sciadv.abi5075 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Kamikawa, Ryoma Mochizuki, Takako Sakamoto, Mika Tanizawa, Yasuhiro Nakayama, Takuro Onuma, Ryo Cenci, Ugo Moog, Daniel Speak, Samuel Sarkozi, Krisztina Toseland, Andrew van Oosterhout, Cock Oyama, Kaori Kato, Misako Kume, Keitaro Kayama, Motoki Azuma, Tomonori Ishii, Ken-ichiro Miyashita, Hideaki Henrissat, Bernard Lombard, Vincent Win, Joe Kamoun, Sophien Kashiyama, Yuichiro Mayama, Shigeki Miyagishima, Shin-ya Tanifuji, Goro Mock, Thomas Nakamura, Yasukazu Genome evolution of a nonparasitic secondary heterotroph, the diatom Nitzschia putrida |
title | Genome evolution of a nonparasitic secondary heterotroph, the diatom Nitzschia putrida |
title_full | Genome evolution of a nonparasitic secondary heterotroph, the diatom Nitzschia putrida |
title_fullStr | Genome evolution of a nonparasitic secondary heterotroph, the diatom Nitzschia putrida |
title_full_unstemmed | Genome evolution of a nonparasitic secondary heterotroph, the diatom Nitzschia putrida |
title_short | Genome evolution of a nonparasitic secondary heterotroph, the diatom Nitzschia putrida |
title_sort | genome evolution of a nonparasitic secondary heterotroph, the diatom nitzschia putrida |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054022/ https://www.ncbi.nlm.nih.gov/pubmed/35486731 http://dx.doi.org/10.1126/sciadv.abi5075 |
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