Identification of the endangered Australian orchid Microtis angusii using an allele-specific PCR assay
The endangered orchid, Microtis angusii, was recently described from a single population consisting of approximately 100 plants. This species is morphologically very similar to close relatives, and taxonomic difficulties have hindered attempts to identify further populations for protection. Here we...
Gespeichert in:
Veröffentlicht in: | Conservation genetics 2007-06, Vol.8 (3), p.721-725 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 725 |
---|---|
container_issue | 3 |
container_start_page | 721 |
container_title | Conservation genetics |
container_volume | 8 |
creator | Flanagan, Nicola S. Peakall, Rod Clements, Mark A. Otero, J. Tupac |
description | The endangered orchid, Microtis angusii, was recently described from a single population consisting of approximately 100 plants. This species is morphologically very similar to close relatives, and taxonomic difficulties have hindered attempts to identify further populations for protection. Here we present a rapid, economical, PCR-based assay for the effective identification of this species based on rDNA sequence variation. Using two single nucleotide substitutions in the internal transcribed spacer (ITS) region of the ribosomal DNA that are diagnostic for M. angusii, we developed an allele-specific PCR that can be easily visualized on a standard agarose gel, avoiding the use of expensive restriction enzymes and DNA sequencing reagents and equipment. Using PCR primer pairs for both the M. angusii, and the alternate allele, we also detected an individual heterozygous for the two alleles, indicating a need for further detailed genetic study. We performed a ‘blind trial’ to confirm the utility of this assay. Microtis angusii samples were successfully discriminated from amongst several congeners, and a further, previously unknown, population of the species was identified. |
doi_str_mv | 10.1007/s10592-006-9198-6 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_19646493</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>19646493</sourcerecordid><originalsourceid>FETCH-LOGICAL-c303t-58d84a52e492ed076db51b8010357b03620df906216c752d5594283f94443e5b3</originalsourceid><addsrcrecordid>eNpdkDtPwzAUhS0EEqXwA9gsBjbDtR3b8VhVPCoVgRDMlhM7ras0KXYy9N_jqEws96H76eieg9AthQcKoB4TBaEZAZBEU10SeYZmVChGtOLqfJqlJCAZvURXKe0AqGSKzlCzcr4bQhNqO4S-w32Dh63HvnO22_joHV6MaYi2DTYfY70NDr-FOvZDSDgjYwoB59Jt8oZt2_rWk3Tw9SSJP5af2KZkj9foorFt8jd_fY6-n5--lq9k_f6yWi7WpObAByJKVxZWMF9o5h0o6SpBqxIocKEq4JKBa_RkQ9ZKMCeELljJG10UBfei4nN0f9I9xP5n9Gkw-5Bq37a28_2YDNWykIXmGbz7B-76MXb5N6MEz3qK6QzRE5T9phR9Yw4x7G08Ggpmit2cYjc5djPFbiT_BT4JdHc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>753944729</pqid></control><display><type>article</type><title>Identification of the endangered Australian orchid Microtis angusii using an allele-specific PCR assay</title><source>SpringerLink Journals - AutoHoldings</source><creator>Flanagan, Nicola S. ; Peakall, Rod ; Clements, Mark A. ; Otero, J. Tupac</creator><creatorcontrib>Flanagan, Nicola S. ; Peakall, Rod ; Clements, Mark A. ; Otero, J. Tupac</creatorcontrib><description>The endangered orchid, Microtis angusii, was recently described from a single population consisting of approximately 100 plants. This species is morphologically very similar to close relatives, and taxonomic difficulties have hindered attempts to identify further populations for protection. Here we present a rapid, economical, PCR-based assay for the effective identification of this species based on rDNA sequence variation. Using two single nucleotide substitutions in the internal transcribed spacer (ITS) region of the ribosomal DNA that are diagnostic for M. angusii, we developed an allele-specific PCR that can be easily visualized on a standard agarose gel, avoiding the use of expensive restriction enzymes and DNA sequencing reagents and equipment. Using PCR primer pairs for both the M. angusii, and the alternate allele, we also detected an individual heterozygous for the two alleles, indicating a need for further detailed genetic study. We performed a ‘blind trial’ to confirm the utility of this assay. Microtis angusii samples were successfully discriminated from amongst several congeners, and a further, previously unknown, population of the species was identified.</description><identifier>ISSN: 1566-0621</identifier><identifier>EISSN: 1572-9737</identifier><identifier>DOI: 10.1007/s10592-006-9198-6</identifier><language>eng</language><publisher>Dordrecht: Springer Nature B.V</publisher><subject>Alleles ; Assaying ; Congeners ; Deoxyribonucleic acid ; DNA ; DNA sequencing ; Equipment costs ; Gene sequencing ; Genetics ; Nucleotides ; Orchidaceae ; Polymerase chain reaction ; Reagents ; Ribosomal DNA ; Species</subject><ispartof>Conservation genetics, 2007-06, Vol.8 (3), p.721-725</ispartof><rights>Springer Science+Business Media B.V. 2006.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c303t-58d84a52e492ed076db51b8010357b03620df906216c752d5594283f94443e5b3</citedby><cites>FETCH-LOGICAL-c303t-58d84a52e492ed076db51b8010357b03620df906216c752d5594283f94443e5b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Flanagan, Nicola S.</creatorcontrib><creatorcontrib>Peakall, Rod</creatorcontrib><creatorcontrib>Clements, Mark A.</creatorcontrib><creatorcontrib>Otero, J. Tupac</creatorcontrib><title>Identification of the endangered Australian orchid Microtis angusii using an allele-specific PCR assay</title><title>Conservation genetics</title><description>The endangered orchid, Microtis angusii, was recently described from a single population consisting of approximately 100 plants. This species is morphologically very similar to close relatives, and taxonomic difficulties have hindered attempts to identify further populations for protection. Here we present a rapid, economical, PCR-based assay for the effective identification of this species based on rDNA sequence variation. Using two single nucleotide substitutions in the internal transcribed spacer (ITS) region of the ribosomal DNA that are diagnostic for M. angusii, we developed an allele-specific PCR that can be easily visualized on a standard agarose gel, avoiding the use of expensive restriction enzymes and DNA sequencing reagents and equipment. Using PCR primer pairs for both the M. angusii, and the alternate allele, we also detected an individual heterozygous for the two alleles, indicating a need for further detailed genetic study. We performed a ‘blind trial’ to confirm the utility of this assay. Microtis angusii samples were successfully discriminated from amongst several congeners, and a further, previously unknown, population of the species was identified.</description><subject>Alleles</subject><subject>Assaying</subject><subject>Congeners</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA sequencing</subject><subject>Equipment costs</subject><subject>Gene sequencing</subject><subject>Genetics</subject><subject>Nucleotides</subject><subject>Orchidaceae</subject><subject>Polymerase chain reaction</subject><subject>Reagents</subject><subject>Ribosomal DNA</subject><subject>Species</subject><issn>1566-0621</issn><issn>1572-9737</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpdkDtPwzAUhS0EEqXwA9gsBjbDtR3b8VhVPCoVgRDMlhM7ras0KXYy9N_jqEws96H76eieg9AthQcKoB4TBaEZAZBEU10SeYZmVChGtOLqfJqlJCAZvURXKe0AqGSKzlCzcr4bQhNqO4S-w32Dh63HvnO22_joHV6MaYi2DTYfY70NDr-FOvZDSDgjYwoB59Jt8oZt2_rWk3Tw9SSJP5af2KZkj9foorFt8jd_fY6-n5--lq9k_f6yWi7WpObAByJKVxZWMF9o5h0o6SpBqxIocKEq4JKBa_RkQ9ZKMCeELljJG10UBfei4nN0f9I9xP5n9Gkw-5Bq37a28_2YDNWykIXmGbz7B-76MXb5N6MEz3qK6QzRE5T9phR9Yw4x7G08Ggpmit2cYjc5djPFbiT_BT4JdHc</recordid><startdate>20070601</startdate><enddate>20070601</enddate><creator>Flanagan, Nicola S.</creator><creator>Peakall, Rod</creator><creator>Clements, Mark A.</creator><creator>Otero, J. Tupac</creator><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7SN</scope><scope>7SS</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</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>C1K</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>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope></search><sort><creationdate>20070601</creationdate><title>Identification of the endangered Australian orchid Microtis angusii using an allele-specific PCR assay</title><author>Flanagan, Nicola S. ; Peakall, Rod ; Clements, Mark A. ; Otero, J. Tupac</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c303t-58d84a52e492ed076db51b8010357b03620df906216c752d5594283f94443e5b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Alleles</topic><topic>Assaying</topic><topic>Congeners</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA sequencing</topic><topic>Equipment costs</topic><topic>Gene sequencing</topic><topic>Genetics</topic><topic>Nucleotides</topic><topic>Orchidaceae</topic><topic>Polymerase chain reaction</topic><topic>Reagents</topic><topic>Ribosomal DNA</topic><topic>Species</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Flanagan, Nicola S.</creatorcontrib><creatorcontrib>Peakall, Rod</creatorcontrib><creatorcontrib>Clements, Mark A.</creatorcontrib><creatorcontrib>Otero, J. Tupac</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Technology Research Database</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</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>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><jtitle>Conservation genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Flanagan, Nicola S.</au><au>Peakall, Rod</au><au>Clements, Mark A.</au><au>Otero, J. Tupac</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of the endangered Australian orchid Microtis angusii using an allele-specific PCR assay</atitle><jtitle>Conservation genetics</jtitle><date>2007-06-01</date><risdate>2007</risdate><volume>8</volume><issue>3</issue><spage>721</spage><epage>725</epage><pages>721-725</pages><issn>1566-0621</issn><eissn>1572-9737</eissn><abstract>The endangered orchid, Microtis angusii, was recently described from a single population consisting of approximately 100 plants. This species is morphologically very similar to close relatives, and taxonomic difficulties have hindered attempts to identify further populations for protection. Here we present a rapid, economical, PCR-based assay for the effective identification of this species based on rDNA sequence variation. Using two single nucleotide substitutions in the internal transcribed spacer (ITS) region of the ribosomal DNA that are diagnostic for M. angusii, we developed an allele-specific PCR that can be easily visualized on a standard agarose gel, avoiding the use of expensive restriction enzymes and DNA sequencing reagents and equipment. Using PCR primer pairs for both the M. angusii, and the alternate allele, we also detected an individual heterozygous for the two alleles, indicating a need for further detailed genetic study. We performed a ‘blind trial’ to confirm the utility of this assay. Microtis angusii samples were successfully discriminated from amongst several congeners, and a further, previously unknown, population of the species was identified.</abstract><cop>Dordrecht</cop><pub>Springer Nature B.V</pub><doi>10.1007/s10592-006-9198-6</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1566-0621 |
ispartof | Conservation genetics, 2007-06, Vol.8 (3), p.721-725 |
issn | 1566-0621 1572-9737 |
language | eng |
recordid | cdi_proquest_miscellaneous_19646493 |
source | SpringerLink Journals - AutoHoldings |
subjects | Alleles Assaying Congeners Deoxyribonucleic acid DNA DNA sequencing Equipment costs Gene sequencing Genetics Nucleotides Orchidaceae Polymerase chain reaction Reagents Ribosomal DNA Species |
title | Identification of the endangered Australian orchid Microtis angusii using an allele-specific PCR assay |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T02%3A42%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Identification%20of%20the%20endangered%20Australian%20orchid%20Microtis%20angusii%20using%20an%20allele-specific%20PCR%20assay&rft.jtitle=Conservation%20genetics&rft.au=Flanagan,%20Nicola%20S.&rft.date=2007-06-01&rft.volume=8&rft.issue=3&rft.spage=721&rft.epage=725&rft.pages=721-725&rft.issn=1566-0621&rft.eissn=1572-9737&rft_id=info:doi/10.1007/s10592-006-9198-6&rft_dat=%3Cproquest_cross%3E19646493%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=753944729&rft_id=info:pmid/&rfr_iscdi=true |