Periodic and coordinated gene expression between a diazotroph and its diatom host
In the surface ocean, light fuels photosynthetic carbon fixation of phytoplankton, playing a critical role in ecosystem processes including carbon export to the deep sea. In oligotrophic oceans, diatom–diazotroph associations (DDAs) play a keystone role in ecosystem function because diazotrophs can...
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description | In the surface ocean, light fuels photosynthetic carbon fixation of phytoplankton, playing a critical role in ecosystem processes including carbon export to the deep sea. In oligotrophic oceans, diatom–diazotroph associations (DDAs) play a keystone role in ecosystem function because diazotrophs can provide otherwise scarce biologically available nitrogen to the diatom host, fueling growth and subsequent carbon sequestration. Despite their importance, relatively little is known about the nature of these associations
in situ
. Here we used metatranscriptomic sequencing of surface samples from the North Pacific Subtropical Gyre (NPSG) to reconstruct patterns of gene expression for the diazotrophic symbiont
Richelia
and we examined how these patterns were integrated with those of the diatom host over day–night transitions.
Richelia
exhibited significant diel signals for genes related to photosynthesis, N
2
fixation, and resource acquisition, among other processes. N
2
fixation genes were significantly co-expressed with host nitrogen uptake and metabolism, as well as potential genes involved in carbon transport, which may underpin the exchange of nitrogen and carbon within this association. Patterns of expression suggested cell division was integrated between the host and symbiont across the diel cycle. Collectively these data suggest that symbiont–host physiological ecology is strongly interconnected in the NPSG. |
doi_str_mv | 10.1038/s41396-018-0262-2 |
format | Article |
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in situ
. Here we used metatranscriptomic sequencing of surface samples from the North Pacific Subtropical Gyre (NPSG) to reconstruct patterns of gene expression for the diazotrophic symbiont
Richelia
and we examined how these patterns were integrated with those of the diatom host over day–night transitions.
Richelia
exhibited significant diel signals for genes related to photosynthesis, N
2
fixation, and resource acquisition, among other processes. N
2
fixation genes were significantly co-expressed with host nitrogen uptake and metabolism, as well as potential genes involved in carbon transport, which may underpin the exchange of nitrogen and carbon within this association. Patterns of expression suggested cell division was integrated between the host and symbiont across the diel cycle. Collectively these data suggest that symbiont–host physiological ecology is strongly interconnected in the NPSG.</description><identifier>ISSN: 1751-7362</identifier><identifier>EISSN: 1751-7370</identifier><identifier>DOI: 10.1038/s41396-018-0262-2</identifier><identifier>PMID: 30116042</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>45/90 ; 631/326/171/1878 ; 704/158/855 ; Biomedical and Life Sciences ; Carbon ; Carbon - metabolism ; Carbon fixation ; Carbon Sequestration ; Cell division ; Cyanobacteria - genetics ; Cyanobacteria - physiology ; Deep sea ; Deep sea environments ; Diatoms - microbiology ; Ecological function ; Ecology ; Ecophysiology ; Ecosystem ; Evolutionary Biology ; Gene expression ; Gene Expression Regulation ; Genes ; Life Sciences ; Marine ecosystems ; Metabolism ; Microbial Ecology ; Microbial Genetics and Genomics ; Microbiology ; Nitrogen ; Nitrogen - metabolism ; Nitrogen fixation ; Nitrogen Fixation - physiology ; Nitrogenation ; Oceans ; Oceans and Seas ; Photosynthesis ; Physiological ecology ; Phytoplankton ; Phytoplankton - metabolism ; Seawater ; Symbiosis</subject><ispartof>The ISME Journal, 2019-01, Vol.13 (1), p.118-131</ispartof><rights>International Society for Microbial Ecology 2018</rights><rights>Copyright Nature Publishing Group Jan 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c536t-8882b0387e9f31c95f157ae2015aaf3a55030cbc8392e0f8ec20ba08b0dd10203</citedby><cites>FETCH-LOGICAL-c536t-8882b0387e9f31c95f157ae2015aaf3a55030cbc8392e0f8ec20ba08b0dd10203</cites><orcidid>0000-0003-3451-3042 ; 0000-0002-5691-5408</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299110/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299110/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30116042$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Harke, Matthew J.</creatorcontrib><creatorcontrib>Frischkorn, Kyle R.</creatorcontrib><creatorcontrib>Haley, Sheean T.</creatorcontrib><creatorcontrib>Aylward, Frank O.</creatorcontrib><creatorcontrib>Zehr, Jonathan P.</creatorcontrib><creatorcontrib>Dyhrman, Sonya T.</creatorcontrib><title>Periodic and coordinated gene expression between a diazotroph and its diatom host</title><title>The ISME Journal</title><addtitle>ISME J</addtitle><addtitle>ISME J</addtitle><description>In the surface ocean, light fuels photosynthetic carbon fixation of phytoplankton, playing a critical role in ecosystem processes including carbon export to the deep sea. In oligotrophic oceans, diatom–diazotroph associations (DDAs) play a keystone role in ecosystem function because diazotrophs can provide otherwise scarce biologically available nitrogen to the diatom host, fueling growth and subsequent carbon sequestration. Despite their importance, relatively little is known about the nature of these associations
in situ
. Here we used metatranscriptomic sequencing of surface samples from the North Pacific Subtropical Gyre (NPSG) to reconstruct patterns of gene expression for the diazotrophic symbiont
Richelia
and we examined how these patterns were integrated with those of the diatom host over day–night transitions.
Richelia
exhibited significant diel signals for genes related to photosynthesis, N
2
fixation, and resource acquisition, among other processes. N
2
fixation genes were significantly co-expressed with host nitrogen uptake and metabolism, as well as potential genes involved in carbon transport, which may underpin the exchange of nitrogen and carbon within this association. Patterns of expression suggested cell division was integrated between the host and symbiont across the diel cycle. Collectively these data suggest that symbiont–host physiological ecology is strongly interconnected in the NPSG.</description><subject>45/90</subject><subject>631/326/171/1878</subject><subject>704/158/855</subject><subject>Biomedical and Life Sciences</subject><subject>Carbon</subject><subject>Carbon - metabolism</subject><subject>Carbon fixation</subject><subject>Carbon Sequestration</subject><subject>Cell division</subject><subject>Cyanobacteria - genetics</subject><subject>Cyanobacteria - physiology</subject><subject>Deep sea</subject><subject>Deep sea environments</subject><subject>Diatoms - microbiology</subject><subject>Ecological function</subject><subject>Ecology</subject><subject>Ecophysiology</subject><subject>Ecosystem</subject><subject>Evolutionary Biology</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Genes</subject><subject>Life Sciences</subject><subject>Marine ecosystems</subject><subject>Metabolism</subject><subject>Microbial Ecology</subject><subject>Microbial Genetics and Genomics</subject><subject>Microbiology</subject><subject>Nitrogen</subject><subject>Nitrogen - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The ISME Journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Harke, Matthew J.</au><au>Frischkorn, Kyle R.</au><au>Haley, Sheean T.</au><au>Aylward, Frank O.</au><au>Zehr, Jonathan P.</au><au>Dyhrman, Sonya T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Periodic and coordinated gene expression between a diazotroph and its diatom host</atitle><jtitle>The ISME Journal</jtitle><stitle>ISME J</stitle><addtitle>ISME J</addtitle><date>2019-01-01</date><risdate>2019</risdate><volume>13</volume><issue>1</issue><spage>118</spage><epage>131</epage><pages>118-131</pages><issn>1751-7362</issn><eissn>1751-7370</eissn><abstract>In the surface ocean, light fuels photosynthetic carbon fixation of phytoplankton, playing a critical role in ecosystem processes including carbon export to the deep sea. In oligotrophic oceans, diatom–diazotroph associations (DDAs) play a keystone role in ecosystem function because diazotrophs can provide otherwise scarce biologically available nitrogen to the diatom host, fueling growth and subsequent carbon sequestration. Despite their importance, relatively little is known about the nature of these associations
in situ
. Here we used metatranscriptomic sequencing of surface samples from the North Pacific Subtropical Gyre (NPSG) to reconstruct patterns of gene expression for the diazotrophic symbiont
Richelia
and we examined how these patterns were integrated with those of the diatom host over day–night transitions.
Richelia
exhibited significant diel signals for genes related to photosynthesis, N
2
fixation, and resource acquisition, among other processes. N
2
fixation genes were significantly co-expressed with host nitrogen uptake and metabolism, as well as potential genes involved in carbon transport, which may underpin the exchange of nitrogen and carbon within this association. Patterns of expression suggested cell division was integrated between the host and symbiont across the diel cycle. Collectively these data suggest that symbiont–host physiological ecology is strongly interconnected in the NPSG.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>30116042</pmid><doi>10.1038/s41396-018-0262-2</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0003-3451-3042</orcidid><orcidid>https://orcid.org/0000-0002-5691-5408</orcidid><oa>free_for_read</oa></addata></record> |
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source | Oxford Journals Open Access Collection; MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | 45/90 631/326/171/1878 704/158/855 Biomedical and Life Sciences Carbon Carbon - metabolism Carbon fixation Carbon Sequestration Cell division Cyanobacteria - genetics Cyanobacteria - physiology Deep sea Deep sea environments Diatoms - microbiology Ecological function Ecology Ecophysiology Ecosystem Evolutionary Biology Gene expression Gene Expression Regulation Genes Life Sciences Marine ecosystems Metabolism Microbial Ecology Microbial Genetics and Genomics Microbiology Nitrogen Nitrogen - metabolism Nitrogen fixation Nitrogen Fixation - physiology Nitrogenation Oceans Oceans and Seas Photosynthesis Physiological ecology Phytoplankton Phytoplankton - metabolism Seawater Symbiosis |
title | Periodic and coordinated gene expression between a diazotroph and its diatom host |
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