Ultrabithorax is essential for bacteriocyte development
Symbiosis often entails the emergence of novel adaptive traits in organisms. Microbial symbionts are indispensable for diverse insects via provisioning of essential nutrients, wherein novel host cells and organs for harboring the microbes, called bacteriocytes and bacteriomes, have evolved repeatedl...
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description | Symbiosis often entails the emergence of novel adaptive traits in organisms. Microbial symbionts are indispensable for diverse insects via provisioning of essential nutrients, wherein novel host cells and organs for harboring the microbes, called bacteriocytes and bacteriomes, have evolved repeatedly. Molecular and developmental mechanisms underpinning the emergence of novel symbiotic cells and organs comprise an unsolved question in evolutionary developmental biology. Here, we report that a conserved homeotic gene, Ultrabithorax , plays a pivotal role in the bacteriocyte differentiation in a hemipteran insect Nysius plebeius . During embryonic development, six pairs of aggregated presumptive bacteriocytes appear on both sides of six abdominal segments, incorporate the symbiotic bacteria at the stage of germband retraction, and fuse into a pair of lateral bacteriomes at the stage of germband flip, where bacteriocyte-associated Ultrabithorax expression coincides with the symbiont infection process. Suppression of Ultrabithorax expression by maternal RNA interference results in disappearance of the bacteriocytes and the symbiont localization therein, suggesting that Ultrabithorax is involved in differentiation of the host cells for symbiosis. Suppression of other homeotic genes abdominal-A and Antennapedia disturbs integrity and positioning of the bacteriomes, affecting the configuration of the host organs for symbiosis. Our findings unveil the molecular and developmental mechanisms underlying the bacteriocyte differentiation, which may have evolved either via cooption of the transcription factors for inducing the novel symbiotic cells, or via revival of the developmental pathway for the bacteriocytes that had existed in the ancestral hemipterans.
Among the most fundamental questions in developmental biology is how novel cell types have emerged in the metazoan evolution. Among the most challenging questions in evolutionary biology is how sophisticated symbiotic associations have evolved through less intimate interorganismal interactions. These fundamental biological issues are crystalized in the evolution and development of insectâs bacteriocytes specialized for harboring symbiotic bacteria. Here, we report that a conserved transcription factor Ultrabithorax is essential for bacteriocyte development in an insect, thereby uncovering a molecular mechanism underlying the emergence of the novel host cells for symbiosis. Our finding highlights the importance of |
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Among the most fundamental questions in developmental biology is how novel cell types have emerged in the metazoan evolution. Among the most challenging questions in evolutionary biology is how sophisticated symbiotic associations have evolved through less intimate interorganismal interactions. These fundamental biological issues are crystalized in the evolution and development of insectâs bacteriocytes specialized for harboring symbiotic bacteria. Here, we report that a conserved transcription factor Ultrabithorax is essential for bacteriocyte development in an insect, thereby uncovering a molecular mechanism underlying the emergence of the novel host cells for symbiosis. Our finding highlights the importance of developmental cooption of preexisting transcription factors and sheds new light on a long-lasting enigma in evolutionary developmental biology.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.1503371112</identifier><identifier>PMID: 26170303</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Animalia ; Animals ; Bacteria ; bacteriocyte ; bacteriocytes ; Base Sequence ; Biological Sciences ; Cells ; Cloning, Molecular ; Drosophila Proteins - physiology ; evolution ; Evolution, Molecular ; Evolutionary biology ; Female ; Gene Expression Profiling ; Gene Expression Regulation, Developmental ; Genes ; Hemiptera - microbiology ; Hemiptera - physiology ; Homeodomain Proteins - metabolism ; Homeodomain Proteins - physiology ; homeotic gene ; In Situ Hybridization ; insect development ; Insect Proteins - physiology ; Insects ; Larva - microbiology ; Larva - physiology ; Male ; Microscopy, Electron, Scanning ; microsymbionts ; Molecular Sequence Data ; Nysius ; Phenotype ; Plebeius ; RNA Interference ; Symbiosis ; transcription factor ; transcription factors ; Transcription Factors - metabolism ; Transcription Factors - physiology</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2015-07, Vol.112 (30), p.9376-9381</ispartof><rights>Copyright National Academy of Sciences Jul 28, 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c535t-160a2db3c6286c0bde1215040b83259aa9f8a46be575a5047ab1cacb44933e553</citedby><cites>FETCH-LOGICAL-c535t-160a2db3c6286c0bde1215040b83259aa9f8a46be575a5047ab1cacb44933e553</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/112/30.cover.gif</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4522796/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4522796/$$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/26170303$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Matsuura, Yu</creatorcontrib><creatorcontrib>Yoshitomo Kikuchi</creatorcontrib><creatorcontrib>Toru Miura</creatorcontrib><creatorcontrib>Takema Fukatsu</creatorcontrib><title>Ultrabithorax is essential for bacteriocyte development</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Symbiosis often entails the emergence of novel adaptive traits in organisms. Microbial symbionts are indispensable for diverse insects via provisioning of essential nutrients, wherein novel host cells and organs for harboring the microbes, called bacteriocytes and bacteriomes, have evolved repeatedly. Molecular and developmental mechanisms underpinning the emergence of novel symbiotic cells and organs comprise an unsolved question in evolutionary developmental biology. Here, we report that a conserved homeotic gene, Ultrabithorax , plays a pivotal role in the bacteriocyte differentiation in a hemipteran insect Nysius plebeius . During embryonic development, six pairs of aggregated presumptive bacteriocytes appear on both sides of six abdominal segments, incorporate the symbiotic bacteria at the stage of germband retraction, and fuse into a pair of lateral bacteriomes at the stage of germband flip, where bacteriocyte-associated Ultrabithorax expression coincides with the symbiont infection process. Suppression of Ultrabithorax expression by maternal RNA interference results in disappearance of the bacteriocytes and the symbiont localization therein, suggesting that Ultrabithorax is involved in differentiation of the host cells for symbiosis. Suppression of other homeotic genes abdominal-A and Antennapedia disturbs integrity and positioning of the bacteriomes, affecting the configuration of the host organs for symbiosis. Our findings unveil the molecular and developmental mechanisms underlying the bacteriocyte differentiation, which may have evolved either via cooption of the transcription factors for inducing the novel symbiotic cells, or via revival of the developmental pathway for the bacteriocytes that had existed in the ancestral hemipterans.
Among the most fundamental questions in developmental biology is how novel cell types have emerged in the metazoan evolution. Among the most challenging questions in evolutionary biology is how sophisticated symbiotic associations have evolved through less intimate interorganismal interactions. These fundamental biological issues are crystalized in the evolution and development of insectâs bacteriocytes specialized for harboring symbiotic bacteria. Here, we report that a conserved transcription factor Ultrabithorax is essential for bacteriocyte development in an insect, thereby uncovering a molecular mechanism underlying the emergence of the novel host cells for symbiosis. Our finding highlights the importance of developmental cooption of preexisting transcription factors and sheds new light on a long-lasting enigma in evolutionary developmental biology.</description><subject>Animalia</subject><subject>Animals</subject><subject>Bacteria</subject><subject>bacteriocyte</subject><subject>bacteriocytes</subject><subject>Base Sequence</subject><subject>Biological Sciences</subject><subject>Cells</subject><subject>Cloning, Molecular</subject><subject>Drosophila Proteins - physiology</subject><subject>evolution</subject><subject>Evolution, Molecular</subject><subject>Evolutionary biology</subject><subject>Female</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Genes</subject><subject>Hemiptera - microbiology</subject><subject>Hemiptera - physiology</subject><subject>Homeodomain Proteins - metabolism</subject><subject>Homeodomain Proteins - physiology</subject><subject>homeotic gene</subject><subject>In Situ Hybridization</subject><subject>insect development</subject><subject>Insect Proteins - physiology</subject><subject>Insects</subject><subject>Larva - microbiology</subject><subject>Larva - physiology</subject><subject>Male</subject><subject>Microscopy, Electron, Scanning</subject><subject>microsymbionts</subject><subject>Molecular Sequence Data</subject><subject>Nysius</subject><subject>Phenotype</subject><subject>Plebeius</subject><subject>RNA Interference</subject><subject>Symbiosis</subject><subject>transcription factor</subject><subject>transcription factors</subject><subject>Transcription Factors - metabolism</subject><subject>Transcription Factors - physiology</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1vEzEQhi0EoiFw5gYrceGy7Yy9ttcXpKriS6rEAXK2xo63dbVZB3tT0X-Po4YUuMDJkueZ1-N5GHuJcIqgxdl2onKKEoTQiMgfsQWCwVZ1Bh6zBQDXbd_x7oQ9K-UGAIzs4Sk74Qo1CBALplfjnMnF-Tpl-tHE0oRSwjRHGpsh5caRn0OOyd_NoVmH2zCm7abWn7MnA40lvDicS7b68P7bxaf28svHzxfnl62XQs4tKiC-dsIr3isPbh2Q13E7cL3g0hCZoadOuSC1pHqvyaEn77rOCBGkFEv27j53u3ObsPb16Uyj3ea4oXxnE0X7Z2WK1_Yq3dpOcq6NqgFvDwE5fd-FMttNLD6MI00h7YrFHnXPpZLm36iuu1VK6P9CqxNheF_RN3-hN2mXp7q0PYWVkNXkkp3dUz6nUnIYjl9EsHvVdq_aPqiuHa9-38yR_-W2Aq8PwL7zGIfcCrBGaPVADJQsXeVY7OorhyoNOHAUUvwEdnm23A</recordid><startdate>20150728</startdate><enddate>20150728</enddate><creator>Matsuura, Yu</creator><creator>Yoshitomo Kikuchi</creator><creator>Toru Miura</creator><creator>Takema Fukatsu</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>20150728</creationdate><title>Ultrabithorax is essential for bacteriocyte development</title><author>Matsuura, Yu ; 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Microbial symbionts are indispensable for diverse insects via provisioning of essential nutrients, wherein novel host cells and organs for harboring the microbes, called bacteriocytes and bacteriomes, have evolved repeatedly. Molecular and developmental mechanisms underpinning the emergence of novel symbiotic cells and organs comprise an unsolved question in evolutionary developmental biology. Here, we report that a conserved homeotic gene, Ultrabithorax , plays a pivotal role in the bacteriocyte differentiation in a hemipteran insect Nysius plebeius . During embryonic development, six pairs of aggregated presumptive bacteriocytes appear on both sides of six abdominal segments, incorporate the symbiotic bacteria at the stage of germband retraction, and fuse into a pair of lateral bacteriomes at the stage of germband flip, where bacteriocyte-associated Ultrabithorax expression coincides with the symbiont infection process. Suppression of Ultrabithorax expression by maternal RNA interference results in disappearance of the bacteriocytes and the symbiont localization therein, suggesting that Ultrabithorax is involved in differentiation of the host cells for symbiosis. Suppression of other homeotic genes abdominal-A and Antennapedia disturbs integrity and positioning of the bacteriomes, affecting the configuration of the host organs for symbiosis. Our findings unveil the molecular and developmental mechanisms underlying the bacteriocyte differentiation, which may have evolved either via cooption of the transcription factors for inducing the novel symbiotic cells, or via revival of the developmental pathway for the bacteriocytes that had existed in the ancestral hemipterans.
Among the most fundamental questions in developmental biology is how novel cell types have emerged in the metazoan evolution. Among the most challenging questions in evolutionary biology is how sophisticated symbiotic associations have evolved through less intimate interorganismal interactions. These fundamental biological issues are crystalized in the evolution and development of insectâs bacteriocytes specialized for harboring symbiotic bacteria. Here, we report that a conserved transcription factor Ultrabithorax is essential for bacteriocyte development in an insect, thereby uncovering a molecular mechanism underlying the emergence of the novel host cells for symbiosis. Our finding highlights the importance of developmental cooption of preexisting transcription factors and sheds new light on a long-lasting enigma in evolutionary developmental biology.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>26170303</pmid><doi>10.1073/pnas.1503371112</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animalia Animals Bacteria bacteriocyte bacteriocytes Base Sequence Biological Sciences Cells Cloning, Molecular Drosophila Proteins - physiology evolution Evolution, Molecular Evolutionary biology Female Gene Expression Profiling Gene Expression Regulation, Developmental Genes Hemiptera - microbiology Hemiptera - physiology Homeodomain Proteins - metabolism Homeodomain Proteins - physiology homeotic gene In Situ Hybridization insect development Insect Proteins - physiology Insects Larva - microbiology Larva - physiology Male Microscopy, Electron, Scanning microsymbionts Molecular Sequence Data Nysius Phenotype Plebeius RNA Interference Symbiosis transcription factor transcription factors Transcription Factors - metabolism Transcription Factors - physiology |
title | Ultrabithorax is essential for bacteriocyte development |
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