Cargando…

Recent transfer of an iron-regulated gene from the plastid to the nuclear genome in an oceanic diatom adapted to chronic iron limitation

BACKGROUND: Although the importance and widespread occurrence of iron limitation in the contemporary ocean is well documented, we still know relatively little about genetic adaptation of phytoplankton to these environments. Compared to its coastal relative Thalassiosira pseudonana, the oceanic diato...

Descripción completa

Detalles Bibliográficos
Autores principales: Lommer, Markus, Roy, Alexandra-Sophie, Schilhabel, Markus, Schreiber, Stefan, Rosenstiel, Philip, LaRoche, Julie
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3022921/
https://www.ncbi.nlm.nih.gov/pubmed/21171997
http://dx.doi.org/10.1186/1471-2164-11-718
_version_ 1782196621282377728
author Lommer, Markus
Roy, Alexandra-Sophie
Schilhabel, Markus
Schreiber, Stefan
Rosenstiel, Philip
LaRoche, Julie
author_facet Lommer, Markus
Roy, Alexandra-Sophie
Schilhabel, Markus
Schreiber, Stefan
Rosenstiel, Philip
LaRoche, Julie
author_sort Lommer, Markus
collection PubMed
description BACKGROUND: Although the importance and widespread occurrence of iron limitation in the contemporary ocean is well documented, we still know relatively little about genetic adaptation of phytoplankton to these environments. Compared to its coastal relative Thalassiosira pseudonana, the oceanic diatom Thalassiosira oceanica is highly tolerant to iron limitation. The adaptation to low-iron conditions in T. oceanica has been attributed to a decrease in the photosynthetic components that are rich in iron. Genomic information on T. oceanica may shed light on the genetic basis of the physiological differences between the two species. RESULTS: The complete 141790 bp sequence of the T. oceanica chloroplast genome [GenBank: GU323224], assembled from massively parallel pyrosequencing (454) shotgun reads, revealed that the petF gene encoding for ferredoxin, which is localized in the chloroplast genome in T. pseudonana and other diatoms, has been transferred to the nucleus in T. oceanica. The iron-sulfur protein ferredoxin, a key element of the chloroplast electron transport chain, can be replaced by the iron-free flavodoxin under iron-limited growth conditions thereby contributing to a reduction in the cellular iron requirements. From a comparison to the genomic context of the T. pseudonana petF gene, the T. oceanica ortholog can be traced back to its chloroplast origin. The coding potential of the T. oceanica chloroplast genome is comparable to that of T. pseudonana and Phaeodactylum tricornutum, though a novel expressed ORF appears in the genomic region that has been subjected to rearrangements linked to the petF gene transfer event. CONCLUSIONS: The transfer of the petF from the cp to the nuclear genome in T. oceanica represents a major difference between the two closely related species. The ability of T. oceanica to tolerate iron limitation suggests that the transfer of petF from the chloroplast to the nuclear genome might have contributed to the ecological success of this species.
format Text
id pubmed-3022921
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-30229212011-01-19 Recent transfer of an iron-regulated gene from the plastid to the nuclear genome in an oceanic diatom adapted to chronic iron limitation Lommer, Markus Roy, Alexandra-Sophie Schilhabel, Markus Schreiber, Stefan Rosenstiel, Philip LaRoche, Julie BMC Genomics Research Article BACKGROUND: Although the importance and widespread occurrence of iron limitation in the contemporary ocean is well documented, we still know relatively little about genetic adaptation of phytoplankton to these environments. Compared to its coastal relative Thalassiosira pseudonana, the oceanic diatom Thalassiosira oceanica is highly tolerant to iron limitation. The adaptation to low-iron conditions in T. oceanica has been attributed to a decrease in the photosynthetic components that are rich in iron. Genomic information on T. oceanica may shed light on the genetic basis of the physiological differences between the two species. RESULTS: The complete 141790 bp sequence of the T. oceanica chloroplast genome [GenBank: GU323224], assembled from massively parallel pyrosequencing (454) shotgun reads, revealed that the petF gene encoding for ferredoxin, which is localized in the chloroplast genome in T. pseudonana and other diatoms, has been transferred to the nucleus in T. oceanica. The iron-sulfur protein ferredoxin, a key element of the chloroplast electron transport chain, can be replaced by the iron-free flavodoxin under iron-limited growth conditions thereby contributing to a reduction in the cellular iron requirements. From a comparison to the genomic context of the T. pseudonana petF gene, the T. oceanica ortholog can be traced back to its chloroplast origin. The coding potential of the T. oceanica chloroplast genome is comparable to that of T. pseudonana and Phaeodactylum tricornutum, though a novel expressed ORF appears in the genomic region that has been subjected to rearrangements linked to the petF gene transfer event. CONCLUSIONS: The transfer of the petF from the cp to the nuclear genome in T. oceanica represents a major difference between the two closely related species. The ability of T. oceanica to tolerate iron limitation suggests that the transfer of petF from the chloroplast to the nuclear genome might have contributed to the ecological success of this species. BioMed Central 2010-12-20 /pmc/articles/PMC3022921/ /pubmed/21171997 http://dx.doi.org/10.1186/1471-2164-11-718 Text en Copyright ©2010 Lommer et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lommer, Markus
Roy, Alexandra-Sophie
Schilhabel, Markus
Schreiber, Stefan
Rosenstiel, Philip
LaRoche, Julie
Recent transfer of an iron-regulated gene from the plastid to the nuclear genome in an oceanic diatom adapted to chronic iron limitation
title Recent transfer of an iron-regulated gene from the plastid to the nuclear genome in an oceanic diatom adapted to chronic iron limitation
title_full Recent transfer of an iron-regulated gene from the plastid to the nuclear genome in an oceanic diatom adapted to chronic iron limitation
title_fullStr Recent transfer of an iron-regulated gene from the plastid to the nuclear genome in an oceanic diatom adapted to chronic iron limitation
title_full_unstemmed Recent transfer of an iron-regulated gene from the plastid to the nuclear genome in an oceanic diatom adapted to chronic iron limitation
title_short Recent transfer of an iron-regulated gene from the plastid to the nuclear genome in an oceanic diatom adapted to chronic iron limitation
title_sort recent transfer of an iron-regulated gene from the plastid to the nuclear genome in an oceanic diatom adapted to chronic iron limitation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3022921/
https://www.ncbi.nlm.nih.gov/pubmed/21171997
http://dx.doi.org/10.1186/1471-2164-11-718
work_keys_str_mv AT lommermarkus recenttransferofanironregulatedgenefromtheplastidtothenucleargenomeinanoceanicdiatomadaptedtochronicironlimitation
AT royalexandrasophie recenttransferofanironregulatedgenefromtheplastidtothenucleargenomeinanoceanicdiatomadaptedtochronicironlimitation
AT schilhabelmarkus recenttransferofanironregulatedgenefromtheplastidtothenucleargenomeinanoceanicdiatomadaptedtochronicironlimitation
AT schreiberstefan recenttransferofanironregulatedgenefromtheplastidtothenucleargenomeinanoceanicdiatomadaptedtochronicironlimitation
AT rosenstielphilip recenttransferofanironregulatedgenefromtheplastidtothenucleargenomeinanoceanicdiatomadaptedtochronicironlimitation
AT larochejulie recenttransferofanironregulatedgenefromtheplastidtothenucleargenomeinanoceanicdiatomadaptedtochronicironlimitation