Gene transfer into insect brain and cell-specific expression of bombyxin gene
A transgene reporter consisting of the bombyxin gene promoter and the green fluorescent protein coding region was introduced into intact brains of the silkworm Bombyx mori by in vitro electroporation. After in vitro culture of the brains, the fluorescence derived from the introduced reporter gene wa...
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Veröffentlicht in: | Development genes and evolution 1999-06, Vol.209 (7), p.447-450 |
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creator | Moto, K Abdel Salam, S E Sakurai, S Iwami, M |
description | A transgene reporter consisting of the bombyxin gene promoter and the green fluorescent protein coding region was introduced into intact brains of the silkworm Bombyx mori by in vitro electroporation. After in vitro culture of the brains, the fluorescence derived from the introduced reporter gene was observed in all cases in eight neurosecretory cells that had previously been identified as bombyxin-producing cells (BPCs). Although the fluorescence was not always observed in all cells, it was specific to BPCs, indicating that the reporter was under the control of the bombyxin gene promoter in a BPC-specific manner. Electroporatical introduction of a reporter gene was therefore found to be a suitable method for analyzing cell-specific expression in intact tissues and to be substitute for germ-line transmission of reporters in the transgenic system. Application of this technique enables us to analyze the cell-specific expression of transgene reporters within a few days and treat more than several dozens of the reporters within 1 month, which is difficult to do with the transgenic system. |
doi_str_mv | 10.1007/s004270050277 |
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After in vitro culture of the brains, the fluorescence derived from the introduced reporter gene was observed in all cases in eight neurosecretory cells that had previously been identified as bombyxin-producing cells (BPCs). Although the fluorescence was not always observed in all cells, it was specific to BPCs, indicating that the reporter was under the control of the bombyxin gene promoter in a BPC-specific manner. Electroporatical introduction of a reporter gene was therefore found to be a suitable method for analyzing cell-specific expression in intact tissues and to be substitute for germ-line transmission of reporters in the transgenic system. Application of this technique enables us to analyze the cell-specific expression of transgene reporters within a few days and treat more than several dozens of the reporters within 1 month, which is difficult to do with the transgenic system.</description><identifier>ISSN: 0949-944X</identifier><identifier>EISSN: 1432-041X</identifier><identifier>DOI: 10.1007/s004270050277</identifier><identifier>PMID: 10370130</identifier><language>eng</language><publisher>Germany: Springer Nature B.V</publisher><subject>Amino Acid Sequence ; Animals ; Bombyx ; Bombyx mori ; Brain ; Brain - physiology ; Cell culture ; Coding ; Electroporation ; Evolutionary genetics ; Fluorescence ; Gene Expression ; Gene transfer ; Gene Transfer Techniques ; Genes, Insect ; Green fluorescent protein ; Molecular Sequence Data ; Neural coding ; Neuropeptides - genetics ; Neurosecretory cells ; Neurotransmission ; Promoters ; Proteins ; Reporter gene ; Transgenes</subject><ispartof>Development genes and evolution, 1999-06, Vol.209 (7), p.447-450</ispartof><rights>Copyright Springer Nature B.V. Jun 1999</rights><rights>Springer-Verlag Berlin Heidelberg 1999</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c376t-5da7dd7e28c346ccb0328c6da8cf49f3b8b118c15f6d25c454dd29e6efa8900e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10370130$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moto, K</creatorcontrib><creatorcontrib>Abdel Salam, S E</creatorcontrib><creatorcontrib>Sakurai, S</creatorcontrib><creatorcontrib>Iwami, M</creatorcontrib><title>Gene transfer into insect brain and cell-specific expression of bombyxin gene</title><title>Development genes and evolution</title><addtitle>Dev Genes Evol</addtitle><description>A transgene reporter consisting of the bombyxin gene promoter and the green fluorescent protein coding region was introduced into intact brains of the silkworm Bombyx mori by in vitro electroporation. After in vitro culture of the brains, the fluorescence derived from the introduced reporter gene was observed in all cases in eight neurosecretory cells that had previously been identified as bombyxin-producing cells (BPCs). Although the fluorescence was not always observed in all cells, it was specific to BPCs, indicating that the reporter was under the control of the bombyxin gene promoter in a BPC-specific manner. Electroporatical introduction of a reporter gene was therefore found to be a suitable method for analyzing cell-specific expression in intact tissues and to be substitute for germ-line transmission of reporters in the transgenic system. Application of this technique enables us to analyze the cell-specific expression of transgene reporters within a few days and treat more than several dozens of the reporters within 1 month, which is difficult to do with the transgenic system.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Bombyx</subject><subject>Bombyx mori</subject><subject>Brain</subject><subject>Brain - physiology</subject><subject>Cell culture</subject><subject>Coding</subject><subject>Electroporation</subject><subject>Evolutionary genetics</subject><subject>Fluorescence</subject><subject>Gene Expression</subject><subject>Gene transfer</subject><subject>Gene Transfer Techniques</subject><subject>Genes, Insect</subject><subject>Green fluorescent protein</subject><subject>Molecular Sequence Data</subject><subject>Neural coding</subject><subject>Neuropeptides - genetics</subject><subject>Neurosecretory cells</subject><subject>Neurotransmission</subject><subject>Promoters</subject><subject>Proteins</subject><subject>Reporter gene</subject><subject>Transgenes</subject><issn>0949-944X</issn><issn>1432-041X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp90UtLAzEUBeAgitbH0q0MCroavXlMHksRrULFjYK7IZPcyJR2piZT0H9vSrtQQTdJFh8nuTmEHFO4pADqKgEIpgAqYEptkREVnJUg6Os2GYERpjRCvO6R_ZSmAJQZXu2SPQpcAeUwIo9j7LAYou1SwFi03dDnJaEbiibatits5wuHs1mZFuja0LoCPxYRU2r7ruhD0fTz5vMjw7ccdEh2gp0lPNrsB-Tl7vb55r6cPI0fbq4npeNKDmXlrfJeIdOOC-lcAzwfpbfaBWECb3RDqXa0CtKzyolKeM8MSgxWGwDkB-RinbuI_fsS01DP27R6pe2wX6baAONSS2WyPP9XSqN5_kaa4ekvOO2XsctT1FoLTSsJIqOzvxCnFRjNmFjdWa6Vi31KEUO9iO3cxs-aQr0qrf5RWvYnm9RlM0f_Ta9b4l9SqZBE</recordid><startdate>19990601</startdate><enddate>19990601</enddate><creator>Moto, K</creator><creator>Abdel Salam, S E</creator><creator>Sakurai, S</creator><creator>Iwami, M</creator><general>Springer Nature B.V</general><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>3V.</scope><scope>7QP</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19990601</creationdate><title>Gene transfer into insect brain and cell-specific expression of bombyxin gene</title><author>Moto, K ; 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After in vitro culture of the brains, the fluorescence derived from the introduced reporter gene was observed in all cases in eight neurosecretory cells that had previously been identified as bombyxin-producing cells (BPCs). Although the fluorescence was not always observed in all cells, it was specific to BPCs, indicating that the reporter was under the control of the bombyxin gene promoter in a BPC-specific manner. Electroporatical introduction of a reporter gene was therefore found to be a suitable method for analyzing cell-specific expression in intact tissues and to be substitute for germ-line transmission of reporters in the transgenic system. 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subjects | Amino Acid Sequence Animals Bombyx Bombyx mori Brain Brain - physiology Cell culture Coding Electroporation Evolutionary genetics Fluorescence Gene Expression Gene transfer Gene Transfer Techniques Genes, Insect Green fluorescent protein Molecular Sequence Data Neural coding Neuropeptides - genetics Neurosecretory cells Neurotransmission Promoters Proteins Reporter gene Transgenes |
title | Gene transfer into insect brain and cell-specific expression of bombyxin gene |
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