Pattern and synchrony of gene expression among sympatric marine microbial populations
Planktonic marine microbes live in dynamic habitats that demand rapid sensing and response to periodic as well as stochastic environmental change. The kinetics, regularity, and specificity of microbial responses in situ, however, are not well-described. We report here simultaneous multitaxon genome-...
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creator | Ottesen, Elizabeth A Young, Curtis R Eppley, John M Ryan, John P Chavez, Francisco P Scholin, Christopher A DeLong, Edward F |
description | Planktonic marine microbes live in dynamic habitats that demand rapid sensing and response to periodic as well as stochastic environmental change. The kinetics, regularity, and specificity of microbial responses in situ, however, are not well-described. We report here simultaneous multitaxon genome-wide transcriptome profiling in a naturally occurring picoplankton community. An in situ robotic sampler using a Lagrangian sampling strategy enabled continuous tracking and repeated sampling of coherent microbial populations over 2 d. Subsequent RNA sequencing analyses yielded genome-wide transcriptome profiles of eukaryotic (Ostreococcus) and bacterial (Synechococcus) photosynthetic picoplankton as well as proteorhodopsin-containing heterotrophs, including Pelagibacter , SAR86-cluster Gammaproteobacteria , and marine Euryarchaea . The photosynthetic picoplankton exhibited strong diel rhythms over thousands of gene transcripts that were remarkably consistent with diel cycling observed in laboratory pure cultures. In contrast, the heterotrophs did not cycle diurnally. Instead, heterotrophic picoplankton populations exhibited cross-species synchronous, tightly regulated, temporally variable patterns of gene expression for many genes, particularly those genes associated with growth and nutrient acquisition. This multitaxon, population-wide gene regulation seemed to reflect sporadic, short-term, reversible responses to high-frequency environmental variability. Although the timing of the environmental responses among different heterotrophic species seemed synchronous, the specific metabolic genes that were expressed varied from taxon to taxon. In aggregate, these results provide insights into the kinetics, diversity, and functional patterns of microbial community response to environmental change. Our results also suggest a means by which complex multispecies metabolic processes could be coordinated, facilitating the regulation of matter and energy processing in a dynamically changing environment. |
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The kinetics, regularity, and specificity of microbial responses in situ, however, are not well-described. We report here simultaneous multitaxon genome-wide transcriptome profiling in a naturally occurring picoplankton community. An in situ robotic sampler using a Lagrangian sampling strategy enabled continuous tracking and repeated sampling of coherent microbial populations over 2 d. Subsequent RNA sequencing analyses yielded genome-wide transcriptome profiles of eukaryotic (Ostreococcus) and bacterial (Synechococcus) photosynthetic picoplankton as well as proteorhodopsin-containing heterotrophs, including Pelagibacter , SAR86-cluster Gammaproteobacteria , and marine Euryarchaea . The photosynthetic picoplankton exhibited strong diel rhythms over thousands of gene transcripts that were remarkably consistent with diel cycling observed in laboratory pure cultures. In contrast, the heterotrophs did not cycle diurnally. Instead, heterotrophic picoplankton populations exhibited cross-species synchronous, tightly regulated, temporally variable patterns of gene expression for many genes, particularly those genes associated with growth and nutrient acquisition. This multitaxon, population-wide gene regulation seemed to reflect sporadic, short-term, reversible responses to high-frequency environmental variability. Although the timing of the environmental responses among different heterotrophic species seemed synchronous, the specific metabolic genes that were expressed varied from taxon to taxon. In aggregate, these results provide insights into the kinetics, diversity, and functional patterns of microbial community response to environmental change. Our results also suggest a means by which complex multispecies metabolic processes could be coordinated, facilitating the regulation of matter and energy processing in a dynamically changing environment.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.1222099110</identifier><identifier>PMID: 23345438</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Archaea - classification ; Archaea - genetics ; Archaea - isolation & purification ; Archaea - metabolism ; Bacteria ; Bacteria - classification ; Bacteria - genetics ; Bacteria - isolation & purification ; Bacteria - metabolism ; Biodiversity ; Biological Sciences ; California ; Circadian Rhythm - genetics ; Ecosystem ; energy ; gamma-Proteobacteria ; Gene expression ; Gene Expression Profiling ; gene expression regulation ; genes ; Genomes ; habitats ; heterotrophs ; messenger RNA ; Metagenome - genetics ; microbial communities ; microorganisms ; Photosynthesis ; Phylogeny ; Physical Sciences ; Phytoplankton - classification ; Phytoplankton - genetics ; Phytoplankton - isolation & purification ; Plankton ; Plankton - classification ; Plankton - genetics ; Plankton - isolation & purification ; PNAS Plus ; Ribonucleic acid ; RNA ; robots ; Seawater - microbiology ; Synechococcus ; Synechococcus - genetics ; Synechococcus - metabolism ; Transcriptome ; transcriptomics ; Water Microbiology</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2013-02, Vol.110 (6), p.E488-E497</ispartof><rights>Copyright National Academy of Sciences Feb 5, 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c567t-e68db9736474cba89fc9095ea80719ca395a82a7f68ae8f11f02f6638c454b793</citedby><cites>FETCH-LOGICAL-c567t-e68db9736474cba89fc9095ea80719ca395a82a7f68ae8f11f02f6638c454b793</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/110/6.cover.gif</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3568374/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3568374/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23345438$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ottesen, Elizabeth A</creatorcontrib><creatorcontrib>Young, Curtis R</creatorcontrib><creatorcontrib>Eppley, John M</creatorcontrib><creatorcontrib>Ryan, John P</creatorcontrib><creatorcontrib>Chavez, Francisco P</creatorcontrib><creatorcontrib>Scholin, Christopher A</creatorcontrib><creatorcontrib>DeLong, Edward F</creatorcontrib><title>Pattern and synchrony of gene expression among sympatric marine microbial populations</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Planktonic marine microbes live in dynamic habitats that demand rapid sensing and response to periodic as well as stochastic environmental change. The kinetics, regularity, and specificity of microbial responses in situ, however, are not well-described. We report here simultaneous multitaxon genome-wide transcriptome profiling in a naturally occurring picoplankton community. An in situ robotic sampler using a Lagrangian sampling strategy enabled continuous tracking and repeated sampling of coherent microbial populations over 2 d. Subsequent RNA sequencing analyses yielded genome-wide transcriptome profiles of eukaryotic (Ostreococcus) and bacterial (Synechococcus) photosynthetic picoplankton as well as proteorhodopsin-containing heterotrophs, including Pelagibacter , SAR86-cluster Gammaproteobacteria , and marine Euryarchaea . The photosynthetic picoplankton exhibited strong diel rhythms over thousands of gene transcripts that were remarkably consistent with diel cycling observed in laboratory pure cultures. In contrast, the heterotrophs did not cycle diurnally. Instead, heterotrophic picoplankton populations exhibited cross-species synchronous, tightly regulated, temporally variable patterns of gene expression for many genes, particularly those genes associated with growth and nutrient acquisition. This multitaxon, population-wide gene regulation seemed to reflect sporadic, short-term, reversible responses to high-frequency environmental variability. Although the timing of the environmental responses among different heterotrophic species seemed synchronous, the specific metabolic genes that were expressed varied from taxon to taxon. In aggregate, these results provide insights into the kinetics, diversity, and functional patterns of microbial community response to environmental change. Our results also suggest a means by which complex multispecies metabolic processes could be coordinated, facilitating the regulation of matter and energy processing in a dynamically changing environment.</description><subject>Archaea - classification</subject><subject>Archaea - genetics</subject><subject>Archaea - isolation & purification</subject><subject>Archaea - metabolism</subject><subject>Bacteria</subject><subject>Bacteria - classification</subject><subject>Bacteria - genetics</subject><subject>Bacteria - isolation & purification</subject><subject>Bacteria - metabolism</subject><subject>Biodiversity</subject><subject>Biological Sciences</subject><subject>California</subject><subject>Circadian Rhythm - genetics</subject><subject>Ecosystem</subject><subject>energy</subject><subject>gamma-Proteobacteria</subject><subject>Gene expression</subject><subject>Gene Expression Profiling</subject><subject>gene expression regulation</subject><subject>genes</subject><subject>Genomes</subject><subject>habitats</subject><subject>heterotrophs</subject><subject>messenger RNA</subject><subject>Metagenome - genetics</subject><subject>microbial communities</subject><subject>microorganisms</subject><subject>Photosynthesis</subject><subject>Phylogeny</subject><subject>Physical Sciences</subject><subject>Phytoplankton - classification</subject><subject>Phytoplankton - genetics</subject><subject>Phytoplankton - isolation & purification</subject><subject>Plankton</subject><subject>Plankton - classification</subject><subject>Plankton - genetics</subject><subject>Plankton - isolation & purification</subject><subject>PNAS Plus</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>robots</subject><subject>Seawater - microbiology</subject><subject>Synechococcus</subject><subject>Synechococcus - genetics</subject><subject>Synechococcus - metabolism</subject><subject>Transcriptome</subject><subject>transcriptomics</subject><subject>Water Microbiology</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0Utv1DAUBWALgehQWLODSGy6SXv9iB8bpKpqoVKlVoJZW47HmbpK7GAniPn3OJoytGxYeeHPR8f3IvQewykGQc_GYPIpJoSAUhjDC7TCoHDNmYKXaAVARC0ZYUfoTc4PAKAaCa_REaGUNYzKFVrfmWlyKVQmbKq8C_Y-xbCrYldtXXCV-zUml7OPBQwxbAsZRjMlb6vBJF_E4G2KrTd9NcZx7s1UbH6LXnWmz-7d43mM1leX3y--1je3X64vzm9q23Ax1Y7LTasE5Uww2xqpOqtKRWckCKysoaoxkhjRcWmc7DDugHScU2lL-1Yoeow-73PHuR3cxrowJdPrMfnSbqej8fr5TfD3eht_atpwSQUrASePASn-mF2e9OCzdX1vgotz1lgCxbhR0PyfEtmAJEzJQj_9Qx_inEKZxKKY5ErwpfzZXpUB5pxcd-iNQS_b1ct29d_tlhcfnn734P-s8wlYXh7iSh7Xl0wu4OMedCZqs00-6_U3ApgDYIZBNvQ3QBq0sg</recordid><startdate>20130205</startdate><enddate>20130205</enddate><creator>Ottesen, Elizabeth A</creator><creator>Young, Curtis R</creator><creator>Eppley, John M</creator><creator>Ryan, John P</creator><creator>Chavez, Francisco P</creator><creator>Scholin, Christopher A</creator><creator>DeLong, Edward F</creator><general>National Academy of Sciences</general><general>National Acad Sciences</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20130205</creationdate><title>Pattern and synchrony of gene expression among sympatric marine microbial populations</title><author>Ottesen, Elizabeth A ; 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The kinetics, regularity, and specificity of microbial responses in situ, however, are not well-described. We report here simultaneous multitaxon genome-wide transcriptome profiling in a naturally occurring picoplankton community. An in situ robotic sampler using a Lagrangian sampling strategy enabled continuous tracking and repeated sampling of coherent microbial populations over 2 d. Subsequent RNA sequencing analyses yielded genome-wide transcriptome profiles of eukaryotic (Ostreococcus) and bacterial (Synechococcus) photosynthetic picoplankton as well as proteorhodopsin-containing heterotrophs, including Pelagibacter , SAR86-cluster Gammaproteobacteria , and marine Euryarchaea . The photosynthetic picoplankton exhibited strong diel rhythms over thousands of gene transcripts that were remarkably consistent with diel cycling observed in laboratory pure cultures. In contrast, the heterotrophs did not cycle diurnally. Instead, heterotrophic picoplankton populations exhibited cross-species synchronous, tightly regulated, temporally variable patterns of gene expression for many genes, particularly those genes associated with growth and nutrient acquisition. This multitaxon, population-wide gene regulation seemed to reflect sporadic, short-term, reversible responses to high-frequency environmental variability. Although the timing of the environmental responses among different heterotrophic species seemed synchronous, the specific metabolic genes that were expressed varied from taxon to taxon. In aggregate, these results provide insights into the kinetics, diversity, and functional patterns of microbial community response to environmental change. Our results also suggest a means by which complex multispecies metabolic processes could be coordinated, facilitating the regulation of matter and energy processing in a dynamically changing environment.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>23345438</pmid><doi>10.1073/pnas.1222099110</doi><oa>free_for_read</oa></addata></record> |
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subjects | Archaea - classification Archaea - genetics Archaea - isolation & purification Archaea - metabolism Bacteria Bacteria - classification Bacteria - genetics Bacteria - isolation & purification Bacteria - metabolism Biodiversity Biological Sciences California Circadian Rhythm - genetics Ecosystem energy gamma-Proteobacteria Gene expression Gene Expression Profiling gene expression regulation genes Genomes habitats heterotrophs messenger RNA Metagenome - genetics microbial communities microorganisms Photosynthesis Phylogeny Physical Sciences Phytoplankton - classification Phytoplankton - genetics Phytoplankton - isolation & purification Plankton Plankton - classification Plankton - genetics Plankton - isolation & purification PNAS Plus Ribonucleic acid RNA robots Seawater - microbiology Synechococcus Synechococcus - genetics Synechococcus - metabolism Transcriptome transcriptomics Water Microbiology |
title | Pattern and synchrony of gene expression among sympatric marine microbial populations |
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