Whole transcriptome analysis of the silicon response of the diatom <it>Thalassiosira pseudonana</it>

<p>Abstract</p> <p>Background</p> <p>Silicon plays important biological roles, but the mechanisms of cellular responses to silicon are poorly understood. We report the first analysis of cell cycle arrest and recovery from silicon starvation in the diatom <it>Thala...

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Main Authors: Shrestha Roshan, Tesson Benoit, Norden-Krichmar Trina, Federowicz Stephen, Hildebrand Mark, Allen Andrew E
Format: Article
Language:English
Published: BMC 2012-09-01
Series:BMC Genomics
Subjects:
Online Access:http://www.biomedcentral.com/1471-2164/13/499
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author Shrestha Roshan
Tesson Benoit
Norden-Krichmar Trina
Federowicz Stephen
Hildebrand Mark
Allen Andrew E
author_facet Shrestha Roshan
Tesson Benoit
Norden-Krichmar Trina
Federowicz Stephen
Hildebrand Mark
Allen Andrew E
author_sort Shrestha Roshan
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Silicon plays important biological roles, but the mechanisms of cellular responses to silicon are poorly understood. We report the first analysis of cell cycle arrest and recovery from silicon starvation in the diatom <it>Thalassiosira pseudonana</it> using whole genome microarrays.</p> <p>Results</p> <p>Three known responses to silicon were examined, 1) silicified cell wall synthesis, 2) recovery from silicon starvation, and 3) co-regulation with silicon transporter (SIT) genes. In terms of diatom cell wall formation, thus far only cell surface proteins and proteins tightly associated with silica have been characterized. Our analysis has identified new genes potentially involved in silica formation, and other genes potentially involved in signaling, trafficking, protein degradation, glycosylation and transport, which provides a larger-scale picture of the processes involved. During silicon starvation, an overrepresentation of transcription and translation related genes were up-regulated, indicating that <it>T. pseudonana</it> is poised to rapidly recover from silicon starvation and resume cell cycle progression upon silicon replenishment. This is in contrast to other types of limitation, and provides the first molecular data explaining the well-established environmental response of diatoms to grow as blooms and to out-compete other classes of microalgae for growth. Comparison of our data with a previous diatom cell cycle analysis indicates that assignment of the cell cycle specific stage of particular cyclins and cyclin dependent kinases should be re-evaluated. Finally, genes co-varying in expression with the SITs enabled identification of a new class of diatom-specific proteins containing a unique domain, and a putative silicon efflux protein.</p> <p>Conclusions</p> <p>Analysis of the <it>T. pseudonana</it> microarray data has provided a wealth of new genes to investigate previously uncharacterized cellular phenomenon related to silicon metabolism, silicon’s interaction with cellular components, and environmental responses to silicon.</p>
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spelling doaj.art-5da16edacf06489c90e7ea74409721c92022-12-22T02:12:27ZengBMCBMC Genomics1471-21642012-09-0113149910.1186/1471-2164-13-499Whole transcriptome analysis of the silicon response of the diatom <it>Thalassiosira pseudonana</it>Shrestha RoshanTesson BenoitNorden-Krichmar TrinaFederowicz StephenHildebrand MarkAllen Andrew E<p>Abstract</p> <p>Background</p> <p>Silicon plays important biological roles, but the mechanisms of cellular responses to silicon are poorly understood. We report the first analysis of cell cycle arrest and recovery from silicon starvation in the diatom <it>Thalassiosira pseudonana</it> using whole genome microarrays.</p> <p>Results</p> <p>Three known responses to silicon were examined, 1) silicified cell wall synthesis, 2) recovery from silicon starvation, and 3) co-regulation with silicon transporter (SIT) genes. In terms of diatom cell wall formation, thus far only cell surface proteins and proteins tightly associated with silica have been characterized. Our analysis has identified new genes potentially involved in silica formation, and other genes potentially involved in signaling, trafficking, protein degradation, glycosylation and transport, which provides a larger-scale picture of the processes involved. During silicon starvation, an overrepresentation of transcription and translation related genes were up-regulated, indicating that <it>T. pseudonana</it> is poised to rapidly recover from silicon starvation and resume cell cycle progression upon silicon replenishment. This is in contrast to other types of limitation, and provides the first molecular data explaining the well-established environmental response of diatoms to grow as blooms and to out-compete other classes of microalgae for growth. Comparison of our data with a previous diatom cell cycle analysis indicates that assignment of the cell cycle specific stage of particular cyclins and cyclin dependent kinases should be re-evaluated. Finally, genes co-varying in expression with the SITs enabled identification of a new class of diatom-specific proteins containing a unique domain, and a putative silicon efflux protein.</p> <p>Conclusions</p> <p>Analysis of the <it>T. pseudonana</it> microarray data has provided a wealth of new genes to investigate previously uncharacterized cellular phenomenon related to silicon metabolism, silicon’s interaction with cellular components, and environmental responses to silicon.</p>http://www.biomedcentral.com/1471-2164/13/499Cell cycleCell wallDiatomMicroarraySilicon effluxSilicon metabolismSilicon transporterSynchrony<it>Thalassiosira pseudonana</it>Transcriptomics
spellingShingle Shrestha Roshan
Tesson Benoit
Norden-Krichmar Trina
Federowicz Stephen
Hildebrand Mark
Allen Andrew E
Whole transcriptome analysis of the silicon response of the diatom <it>Thalassiosira pseudonana</it>
BMC Genomics
Cell cycle
Cell wall
Diatom
Microarray
Silicon efflux
Silicon metabolism
Silicon transporter
Synchrony
<it>Thalassiosira pseudonana</it>
Transcriptomics
title Whole transcriptome analysis of the silicon response of the diatom <it>Thalassiosira pseudonana</it>
title_full Whole transcriptome analysis of the silicon response of the diatom <it>Thalassiosira pseudonana</it>
title_fullStr Whole transcriptome analysis of the silicon response of the diatom <it>Thalassiosira pseudonana</it>
title_full_unstemmed Whole transcriptome analysis of the silicon response of the diatom <it>Thalassiosira pseudonana</it>
title_short Whole transcriptome analysis of the silicon response of the diatom <it>Thalassiosira pseudonana</it>
title_sort whole transcriptome analysis of the silicon response of the diatom it thalassiosira pseudonana it
topic Cell cycle
Cell wall
Diatom
Microarray
Silicon efflux
Silicon metabolism
Silicon transporter
Synchrony
<it>Thalassiosira pseudonana</it>
Transcriptomics
url http://www.biomedcentral.com/1471-2164/13/499
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