Loading…
Routine Utilization of Green Fluorescent Protein as a Visual Selectable Marker for Cereal Transformation
Development of new selectable markers is needed to increase the efficiency and flexibility of plant transformation, and to overcome drawbacks sometimes associated with use of existing markers. A useful alternative to chemical-based selection systems would be a system using visual screening to obtain...
Saved in:
Published in: | In vitro cellular & developmental biology. Plant 2001-03, Vol.37 (2), p.120-126 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c291t-9dcef267bc19036cdd3652cb5630c28c630214621d0ed75981fec6b98f84afee3 |
---|---|
cites | cdi_FETCH-LOGICAL-c291t-9dcef267bc19036cdd3652cb5630c28c630214621d0ed75981fec6b98f84afee3 |
container_end_page | 126 |
container_issue | 2 |
container_start_page | 120 |
container_title | In vitro cellular & developmental biology. Plant |
container_volume | 37 |
creator | Heidi F. Kaeppler A. R. Carlson Menon, G. K. |
description | Development of new selectable markers is needed to increase the efficiency and flexibility of plant transformation, and to overcome drawbacks sometimes associated with use of existing markers. A useful alternative to chemical-based selection systems would be a system using visual screening to obtain transgenic lines. Investigations were carried out to determine if the green fluorescent protein (gfp) gene could be utilized alone as a visual screenable marker to produce stably transformed, fertile oat plants. Twelve experiments were conducted in which gfp-based selection was utilized to obtain routinely stable transgenic lines in oat. A synthetic gfp gene under the control of the maize ubiquitin promoter was delivered into embryogenic oat callus via microprojectile bombardment. Cell clusters (1-3 mm) expressing gfp were visually identified using epifluorescence microscopy and physically isolated approximately 3 wk post-bombardment. Fertile, gfp-expressing T0 plants were regenerated from 78% of the glowing cell sectors placed on regeneration medium. T0 plants from 55% of the events produced gfp-expressing progeny in a 3:1 Mendelian ratio. Southern blot and PCR analysis confirmed transgene integration and transmission to progeny. Expression of gfp did not reduce plant growth or fertility. Transgene copy number and integration patterns were similar to those in transgenic plants derived from chemical-based selection systems. The mean transformation frequency, based on fertile events obtained per bombarded plate, was 1.8%. Over 180 independent transgenic oat lines were produced, to date, using only visual screening for expression of gfp, demonstrating efficiency and repeatability of the selection system. |
doi_str_mv | 10.1007/s11627-001-0023-0 |
format | article |
fullrecord | <record><control><sourceid>jstor_proqu</sourceid><recordid>TN_cdi_proquest_journals_197387771</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>4293432</jstor_id><sourcerecordid>4293432</sourcerecordid><originalsourceid>FETCH-LOGICAL-c291t-9dcef267bc19036cdd3652cb5630c28c630214621d0ed75981fec6b98f84afee3</originalsourceid><addsrcrecordid>eNo9kE9LAzEQxYMoWKsfQPAQvK_mz26yOUrRKlQUbb2GNDvBrdtNTbIH_fSmrngYZoZ57w38EDqn5IoSIq8jpYLJghCai_GCHKAJLWVVMFGrwzyTqiyqUopjdBLjhmQhoXKC3l_8kNoe8Cq1XfttUut77B2eB4Ae33WDDxAt9Ak_B5-g7bGJ2OC3Ng6mw6_QgU1m3QF-NOEDAnY-4BkEyMdlMH3M-_Y39BQdOdNFOPvrU7S6u13O7ovF0_xhdrMoLFM0Faqx4JiQa0sV4cI2DRcVs-tKcGJZbXNjtBSMNgQaWamaOrBirWpXl8YB8Cm6HHN3wX8OEJPe-CH0-aWmSvJaSkmziI4iG3yMAZzehXZrwpemRO956pGnzpj0nqcm2XMxejYx-fBvKJniJWf8ByPhcrM</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>197387771</pqid></control><display><type>article</type><title>Routine Utilization of Green Fluorescent Protein as a Visual Selectable Marker for Cereal Transformation</title><source>JSTOR Archival Journals and Primary Sources Collection</source><source>Springer Link</source><creator>Heidi F. Kaeppler ; A. R. Carlson ; Menon, G. K.</creator><creatorcontrib>Heidi F. Kaeppler ; A. R. Carlson ; Menon, G. K.</creatorcontrib><description>Development of new selectable markers is needed to increase the efficiency and flexibility of plant transformation, and to overcome drawbacks sometimes associated with use of existing markers. A useful alternative to chemical-based selection systems would be a system using visual screening to obtain transgenic lines. Investigations were carried out to determine if the green fluorescent protein (gfp) gene could be utilized alone as a visual screenable marker to produce stably transformed, fertile oat plants. Twelve experiments were conducted in which gfp-based selection was utilized to obtain routinely stable transgenic lines in oat. A synthetic gfp gene under the control of the maize ubiquitin promoter was delivered into embryogenic oat callus via microprojectile bombardment. Cell clusters (1-3 mm) expressing gfp were visually identified using epifluorescence microscopy and physically isolated approximately 3 wk post-bombardment. Fertile, gfp-expressing T0 plants were regenerated from 78% of the glowing cell sectors placed on regeneration medium. T0 plants from 55% of the events produced gfp-expressing progeny in a 3:1 Mendelian ratio. Southern blot and PCR analysis confirmed transgene integration and transmission to progeny. Expression of gfp did not reduce plant growth or fertility. Transgene copy number and integration patterns were similar to those in transgenic plants derived from chemical-based selection systems. The mean transformation frequency, based on fertile events obtained per bombarded plate, was 1.8%. Over 180 independent transgenic oat lines were produced, to date, using only visual screening for expression of gfp, demonstrating efficiency and repeatability of the selection system.</description><identifier>ISSN: 1054-5476</identifier><identifier>EISSN: 1475-2689</identifier><identifier>DOI: 10.1007/s11627-001-0023-0</identifier><language>eng</language><publisher>Heidelberg: CABI Publishing</publisher><subject>Callus ; Cell lines ; Corn ; Genetic screening ; Oats ; Plant cells ; Plant fertility ; Plants ; Special: Workshop: Alternative Markers for Plant Transformation: Workshop Presentations from the 2000 World Congress on In vitro Biology ; Transgenes ; Transgenic plants</subject><ispartof>In vitro cellular & developmental biology. Plant, 2001-03, Vol.37 (2), p.120-126</ispartof><rights>Copyright 2001 The Society for In Vitro Biology</rights><rights>Copyright Society for In Vitro Biology Mar/Apr 2001</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c291t-9dcef267bc19036cdd3652cb5630c28c630214621d0ed75981fec6b98f84afee3</citedby><cites>FETCH-LOGICAL-c291t-9dcef267bc19036cdd3652cb5630c28c630214621d0ed75981fec6b98f84afee3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4293432$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4293432$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,58238,58471</link.rule.ids></links><search><creatorcontrib>Heidi F. Kaeppler</creatorcontrib><creatorcontrib>A. R. Carlson</creatorcontrib><creatorcontrib>Menon, G. K.</creatorcontrib><title>Routine Utilization of Green Fluorescent Protein as a Visual Selectable Marker for Cereal Transformation</title><title>In vitro cellular & developmental biology. Plant</title><description>Development of new selectable markers is needed to increase the efficiency and flexibility of plant transformation, and to overcome drawbacks sometimes associated with use of existing markers. A useful alternative to chemical-based selection systems would be a system using visual screening to obtain transgenic lines. Investigations were carried out to determine if the green fluorescent protein (gfp) gene could be utilized alone as a visual screenable marker to produce stably transformed, fertile oat plants. Twelve experiments were conducted in which gfp-based selection was utilized to obtain routinely stable transgenic lines in oat. A synthetic gfp gene under the control of the maize ubiquitin promoter was delivered into embryogenic oat callus via microprojectile bombardment. Cell clusters (1-3 mm) expressing gfp were visually identified using epifluorescence microscopy and physically isolated approximately 3 wk post-bombardment. Fertile, gfp-expressing T0 plants were regenerated from 78% of the glowing cell sectors placed on regeneration medium. T0 plants from 55% of the events produced gfp-expressing progeny in a 3:1 Mendelian ratio. Southern blot and PCR analysis confirmed transgene integration and transmission to progeny. Expression of gfp did not reduce plant growth or fertility. Transgene copy number and integration patterns were similar to those in transgenic plants derived from chemical-based selection systems. The mean transformation frequency, based on fertile events obtained per bombarded plate, was 1.8%. Over 180 independent transgenic oat lines were produced, to date, using only visual screening for expression of gfp, demonstrating efficiency and repeatability of the selection system.</description><subject>Callus</subject><subject>Cell lines</subject><subject>Corn</subject><subject>Genetic screening</subject><subject>Oats</subject><subject>Plant cells</subject><subject>Plant fertility</subject><subject>Plants</subject><subject>Special: Workshop: Alternative Markers for Plant Transformation: Workshop Presentations from the 2000 World Congress on In vitro Biology</subject><subject>Transgenes</subject><subject>Transgenic plants</subject><issn>1054-5476</issn><issn>1475-2689</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNo9kE9LAzEQxYMoWKsfQPAQvK_mz26yOUrRKlQUbb2GNDvBrdtNTbIH_fSmrngYZoZ57w38EDqn5IoSIq8jpYLJghCai_GCHKAJLWVVMFGrwzyTqiyqUopjdBLjhmQhoXKC3l_8kNoe8Cq1XfttUut77B2eB4Ae33WDDxAt9Ak_B5-g7bGJ2OC3Ng6mw6_QgU1m3QF-NOEDAnY-4BkEyMdlMH3M-_Y39BQdOdNFOPvrU7S6u13O7ovF0_xhdrMoLFM0Faqx4JiQa0sV4cI2DRcVs-tKcGJZbXNjtBSMNgQaWamaOrBirWpXl8YB8Cm6HHN3wX8OEJPe-CH0-aWmSvJaSkmziI4iG3yMAZzehXZrwpemRO956pGnzpj0nqcm2XMxejYx-fBvKJniJWf8ByPhcrM</recordid><startdate>20010301</startdate><enddate>20010301</enddate><creator>Heidi F. Kaeppler</creator><creator>A. R. Carlson</creator><creator>Menon, G. K.</creator><general>CABI Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>4T-</scope><scope>4U-</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>S0X</scope></search><sort><creationdate>20010301</creationdate><title>Routine Utilization of Green Fluorescent Protein as a Visual Selectable Marker for Cereal Transformation</title><author>Heidi F. Kaeppler ; A. R. Carlson ; Menon, G. K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c291t-9dcef267bc19036cdd3652cb5630c28c630214621d0ed75981fec6b98f84afee3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Callus</topic><topic>Cell lines</topic><topic>Corn</topic><topic>Genetic screening</topic><topic>Oats</topic><topic>Plant cells</topic><topic>Plant fertility</topic><topic>Plants</topic><topic>Special: Workshop: Alternative Markers for Plant Transformation: Workshop Presentations from the 2000 World Congress on In vitro Biology</topic><topic>Transgenes</topic><topic>Transgenic plants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Heidi F. Kaeppler</creatorcontrib><creatorcontrib>A. R. Carlson</creatorcontrib><creatorcontrib>Menon, G. K.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><jtitle>In vitro cellular & developmental biology. Plant</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Heidi F. Kaeppler</au><au>A. R. Carlson</au><au>Menon, G. K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Routine Utilization of Green Fluorescent Protein as a Visual Selectable Marker for Cereal Transformation</atitle><jtitle>In vitro cellular & developmental biology. Plant</jtitle><date>2001-03-01</date><risdate>2001</risdate><volume>37</volume><issue>2</issue><spage>120</spage><epage>126</epage><pages>120-126</pages><issn>1054-5476</issn><eissn>1475-2689</eissn><abstract>Development of new selectable markers is needed to increase the efficiency and flexibility of plant transformation, and to overcome drawbacks sometimes associated with use of existing markers. A useful alternative to chemical-based selection systems would be a system using visual screening to obtain transgenic lines. Investigations were carried out to determine if the green fluorescent protein (gfp) gene could be utilized alone as a visual screenable marker to produce stably transformed, fertile oat plants. Twelve experiments were conducted in which gfp-based selection was utilized to obtain routinely stable transgenic lines in oat. A synthetic gfp gene under the control of the maize ubiquitin promoter was delivered into embryogenic oat callus via microprojectile bombardment. Cell clusters (1-3 mm) expressing gfp were visually identified using epifluorescence microscopy and physically isolated approximately 3 wk post-bombardment. Fertile, gfp-expressing T0 plants were regenerated from 78% of the glowing cell sectors placed on regeneration medium. T0 plants from 55% of the events produced gfp-expressing progeny in a 3:1 Mendelian ratio. Southern blot and PCR analysis confirmed transgene integration and transmission to progeny. Expression of gfp did not reduce plant growth or fertility. Transgene copy number and integration patterns were similar to those in transgenic plants derived from chemical-based selection systems. The mean transformation frequency, based on fertile events obtained per bombarded plate, was 1.8%. Over 180 independent transgenic oat lines were produced, to date, using only visual screening for expression of gfp, demonstrating efficiency and repeatability of the selection system.</abstract><cop>Heidelberg</cop><pub>CABI Publishing</pub><doi>10.1007/s11627-001-0023-0</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1054-5476 |
ispartof | In vitro cellular & developmental biology. Plant, 2001-03, Vol.37 (2), p.120-126 |
issn | 1054-5476 1475-2689 |
language | eng |
recordid | cdi_proquest_journals_197387771 |
source | JSTOR Archival Journals and Primary Sources Collection; Springer Link |
subjects | Callus Cell lines Corn Genetic screening Oats Plant cells Plant fertility Plants Special: Workshop: Alternative Markers for Plant Transformation: Workshop Presentations from the 2000 World Congress on In vitro Biology Transgenes Transgenic plants |
title | Routine Utilization of Green Fluorescent Protein as a Visual Selectable Marker for Cereal Transformation |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T06%3A27%3A10IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Routine%20Utilization%20of%20Green%20Fluorescent%20Protein%20as%20a%20Visual%20Selectable%20Marker%20for%20Cereal%20Transformation&rft.jtitle=In%20vitro%20cellular%20&%20developmental%20biology.%20Plant&rft.au=Heidi%20F.%20Kaeppler&rft.date=2001-03-01&rft.volume=37&rft.issue=2&rft.spage=120&rft.epage=126&rft.pages=120-126&rft.issn=1054-5476&rft.eissn=1475-2689&rft_id=info:doi/10.1007/s11627-001-0023-0&rft_dat=%3Cjstor_proqu%3E4293432%3C/jstor_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c291t-9dcef267bc19036cdd3652cb5630c28c630214621d0ed75981fec6b98f84afee3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=197387771&rft_id=info:pmid/&rft_jstor_id=4293432&rfr_iscdi=true |