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Diploid genomic architecture of Nitzschia inconspicua, an elite biomass production diatom

A near-complete diploid nuclear genome and accompanying circular mitochondrial and chloroplast genomes have been assembled from the elite commercial diatom species Nitzschia inconspicua. The 50 Mbp haploid size of the nuclear genome is nearly double that of model diatom Phaeodactylum tricornutum, bu...

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Autores principales: Oliver, Aaron, Podell, Sheila, Pinowska, Agnieszka, Traller, Jesse C., Smith, Sarah R., McClure, Ryan, Beliaev, Alex, Bohutskyi, Pavlo, Hill, Eric A., Rabines, Ariel, Zheng, Hong, Allen, Lisa Zeigler, Kuo, Alan, Grigoriev, Igor V., Allen, Andrew E., Hazlebeck, David, Allen, Eric E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329260/
https://www.ncbi.nlm.nih.gov/pubmed/34341414
http://dx.doi.org/10.1038/s41598-021-95106-3
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author Oliver, Aaron
Podell, Sheila
Pinowska, Agnieszka
Traller, Jesse C.
Smith, Sarah R.
McClure, Ryan
Beliaev, Alex
Bohutskyi, Pavlo
Hill, Eric A.
Rabines, Ariel
Zheng, Hong
Allen, Lisa Zeigler
Kuo, Alan
Grigoriev, Igor V.
Allen, Andrew E.
Hazlebeck, David
Allen, Eric E.
author_facet Oliver, Aaron
Podell, Sheila
Pinowska, Agnieszka
Traller, Jesse C.
Smith, Sarah R.
McClure, Ryan
Beliaev, Alex
Bohutskyi, Pavlo
Hill, Eric A.
Rabines, Ariel
Zheng, Hong
Allen, Lisa Zeigler
Kuo, Alan
Grigoriev, Igor V.
Allen, Andrew E.
Hazlebeck, David
Allen, Eric E.
author_sort Oliver, Aaron
collection PubMed
description A near-complete diploid nuclear genome and accompanying circular mitochondrial and chloroplast genomes have been assembled from the elite commercial diatom species Nitzschia inconspicua. The 50 Mbp haploid size of the nuclear genome is nearly double that of model diatom Phaeodactylum tricornutum, but 30% smaller than closer relative Fragilariopsis cylindrus. Diploid assembly, which was facilitated by low levels of allelic heterozygosity (2.7%), included 14 candidate chromosome pairs composed of long, syntenic contigs, covering 93% of the total assembly. Telomeric ends were capped with an unusual 12-mer, G-rich, degenerate repeat sequence. Predicted proteins were highly enriched in strain-specific marker domains associated with cell-surface adhesion, biofilm formation, and raphe system gliding motility. Expanded species-specific families of carbonic anhydrases suggest potential enhancement of carbon concentration efficiency, and duplicated glycolysis and fatty acid synthesis pathways across cytosolic and organellar compartments may enhance peak metabolic output, contributing to competitive success over other organisms in mixed cultures. The N. inconspicua genome delivers a robust new reference for future functional and transcriptomic studies to illuminate the physiology of benthic pennate diatoms and harness their unique adaptations to support commercial algae biomass and bioproduct production.
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spelling pubmed-83292602021-08-04 Diploid genomic architecture of Nitzschia inconspicua, an elite biomass production diatom Oliver, Aaron Podell, Sheila Pinowska, Agnieszka Traller, Jesse C. Smith, Sarah R. McClure, Ryan Beliaev, Alex Bohutskyi, Pavlo Hill, Eric A. Rabines, Ariel Zheng, Hong Allen, Lisa Zeigler Kuo, Alan Grigoriev, Igor V. Allen, Andrew E. Hazlebeck, David Allen, Eric E. Sci Rep Article A near-complete diploid nuclear genome and accompanying circular mitochondrial and chloroplast genomes have been assembled from the elite commercial diatom species Nitzschia inconspicua. The 50 Mbp haploid size of the nuclear genome is nearly double that of model diatom Phaeodactylum tricornutum, but 30% smaller than closer relative Fragilariopsis cylindrus. Diploid assembly, which was facilitated by low levels of allelic heterozygosity (2.7%), included 14 candidate chromosome pairs composed of long, syntenic contigs, covering 93% of the total assembly. Telomeric ends were capped with an unusual 12-mer, G-rich, degenerate repeat sequence. Predicted proteins were highly enriched in strain-specific marker domains associated with cell-surface adhesion, biofilm formation, and raphe system gliding motility. Expanded species-specific families of carbonic anhydrases suggest potential enhancement of carbon concentration efficiency, and duplicated glycolysis and fatty acid synthesis pathways across cytosolic and organellar compartments may enhance peak metabolic output, contributing to competitive success over other organisms in mixed cultures. The N. inconspicua genome delivers a robust new reference for future functional and transcriptomic studies to illuminate the physiology of benthic pennate diatoms and harness their unique adaptations to support commercial algae biomass and bioproduct production. Nature Publishing Group UK 2021-08-02 /pmc/articles/PMC8329260/ /pubmed/34341414 http://dx.doi.org/10.1038/s41598-021-95106-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Oliver, Aaron
Podell, Sheila
Pinowska, Agnieszka
Traller, Jesse C.
Smith, Sarah R.
McClure, Ryan
Beliaev, Alex
Bohutskyi, Pavlo
Hill, Eric A.
Rabines, Ariel
Zheng, Hong
Allen, Lisa Zeigler
Kuo, Alan
Grigoriev, Igor V.
Allen, Andrew E.
Hazlebeck, David
Allen, Eric E.
Diploid genomic architecture of Nitzschia inconspicua, an elite biomass production diatom
title Diploid genomic architecture of Nitzschia inconspicua, an elite biomass production diatom
title_full Diploid genomic architecture of Nitzschia inconspicua, an elite biomass production diatom
title_fullStr Diploid genomic architecture of Nitzschia inconspicua, an elite biomass production diatom
title_full_unstemmed Diploid genomic architecture of Nitzschia inconspicua, an elite biomass production diatom
title_short Diploid genomic architecture of Nitzschia inconspicua, an elite biomass production diatom
title_sort diploid genomic architecture of nitzschia inconspicua, an elite biomass production diatom
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329260/
https://www.ncbi.nlm.nih.gov/pubmed/34341414
http://dx.doi.org/10.1038/s41598-021-95106-3
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