Cloning and Expression Analysis of MIo Gene from Pericallis hybrida B. Nord
The full-length Mlo gene was obtained by reverse transcription polymerase chain reaction (RT-PCR) and RACE. The result of sequence analysis indicated that M/o gene from Pericallis hybrida B. Nord. contained about 1296bp open reading frame and encoded 431 amino acids. According to the comparison of t...
Gespeichert in:
Veröffentlicht in: | 东北农业大学学报:英文版 2014, Vol.21 (1), p.10-15 |
---|---|
1. Verfasser: | |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 15 |
---|---|
container_issue | 1 |
container_start_page | 10 |
container_title | 东北农业大学学报:英文版 |
container_volume | 21 |
creator | Wang Jin-gan Li Wei Ren Hong-wei Lv Yuan-da Bai Ding Xu Jing |
description | The full-length Mlo gene was obtained by reverse transcription polymerase chain reaction (RT-PCR) and RACE. The result of sequence analysis indicated that M/o gene from Pericallis hybrida B. Nord. contained about 1296bp open reading frame and encoded 431 amino acids. According to the comparison of the exogenous gene sequences by BLAST analysis and phylogenetic analysis, Mlo gene shared over 85% nucleotide homology and 98% amino acid homology. Finally, through semi-quantitative-PCR and fluorescence quantitative analysis, we found that Mlo gene showed the highest expression levels in leaves and the lowest in roots after inoculated with powdery mildew pathogen for different days. |
format | Article |
fullrecord | <record><control><sourceid>chongqing</sourceid><recordid>TN_cdi_chongqing_primary_48901665</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cqvip_id>48901665</cqvip_id><sourcerecordid>48901665</sourcerecordid><originalsourceid>FETCH-chongqing_primary_489016653</originalsourceid><addsrcrecordid>eNpjYeA0NDAw07UwNDDhYOAqLs4C8ozMzA04Gbydc_LzMvPSFRLzUhRcKwqKUouLM_PzFBzzEnMqizOLFfLTFHw98xXcU_NSFdKK8nMVAlKLMpMTc3KAchmVSUWZKYkKTnoKfvlFKTwMrGmJOcWpvFCam0HRzTXE2UM3OSM_L70QaEt8QVFmbmJRZbyJhaWBoZmZqTExagAXzTop</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Cloning and Expression Analysis of MIo Gene from Pericallis hybrida B. Nord</title><source>Alma/SFX Local Collection</source><creator>Wang Jin-gan Li Wei Ren Hong-wei Lv Yuan-da Bai Ding Xu Jing</creator><creatorcontrib>Wang Jin-gan Li Wei Ren Hong-wei Lv Yuan-da Bai Ding Xu Jing</creatorcontrib><description>The full-length Mlo gene was obtained by reverse transcription polymerase chain reaction (RT-PCR) and RACE. The result of sequence analysis indicated that M/o gene from Pericallis hybrida B. Nord. contained about 1296bp open reading frame and encoded 431 amino acids. According to the comparison of the exogenous gene sequences by BLAST analysis and phylogenetic analysis, Mlo gene shared over 85% nucleotide homology and 98% amino acid homology. Finally, through semi-quantitative-PCR and fluorescence quantitative analysis, we found that Mlo gene showed the highest expression levels in leaves and the lowest in roots after inoculated with powdery mildew pathogen for different days.</description><identifier>ISSN: 1006-8104</identifier><language>eng</language><ispartof>东北农业大学学报:英文版, 2014, Vol.21 (1), p.10-15</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/85645X/85645X.jpg</thumbnail><link.rule.ids>314,776,780,4010</link.rule.ids></links><search><creatorcontrib>Wang Jin-gan Li Wei Ren Hong-wei Lv Yuan-da Bai Ding Xu Jing</creatorcontrib><title>Cloning and Expression Analysis of MIo Gene from Pericallis hybrida B. Nord</title><title>东北农业大学学报:英文版</title><addtitle>Journal of Northeast Agricultural University</addtitle><description>The full-length Mlo gene was obtained by reverse transcription polymerase chain reaction (RT-PCR) and RACE. The result of sequence analysis indicated that M/o gene from Pericallis hybrida B. Nord. contained about 1296bp open reading frame and encoded 431 amino acids. According to the comparison of the exogenous gene sequences by BLAST analysis and phylogenetic analysis, Mlo gene shared over 85% nucleotide homology and 98% amino acid homology. Finally, through semi-quantitative-PCR and fluorescence quantitative analysis, we found that Mlo gene showed the highest expression levels in leaves and the lowest in roots after inoculated with powdery mildew pathogen for different days.</description><issn>1006-8104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNpjYeA0NDAw07UwNDDhYOAqLs4C8ozMzA04Gbydc_LzMvPSFRLzUhRcKwqKUouLM_PzFBzzEnMqizOLFfLTFHw98xXcU_NSFdKK8nMVAlKLMpMTc3KAchmVSUWZKYkKTnoKfvlFKTwMrGmJOcWpvFCam0HRzTXE2UM3OSM_L70QaEt8QVFmbmJRZbyJhaWBoZmZqTExagAXzTop</recordid><startdate>2014</startdate><enddate>2014</enddate><creator>Wang Jin-gan Li Wei Ren Hong-wei Lv Yuan-da Bai Ding Xu Jing</creator><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W95</scope><scope>~WA</scope></search><sort><creationdate>2014</creationdate><title>Cloning and Expression Analysis of MIo Gene from Pericallis hybrida B. Nord</title><author>Wang Jin-gan Li Wei Ren Hong-wei Lv Yuan-da Bai Ding Xu Jing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-chongqing_primary_489016653</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Wang Jin-gan Li Wei Ren Hong-wei Lv Yuan-da Bai Ding Xu Jing</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-农业科学</collection><collection>中文科技期刊数据库- 镜像站点</collection><jtitle>东北农业大学学报:英文版</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang Jin-gan Li Wei Ren Hong-wei Lv Yuan-da Bai Ding Xu Jing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cloning and Expression Analysis of MIo Gene from Pericallis hybrida B. Nord</atitle><jtitle>东北农业大学学报:英文版</jtitle><addtitle>Journal of Northeast Agricultural University</addtitle><date>2014</date><risdate>2014</risdate><volume>21</volume><issue>1</issue><spage>10</spage><epage>15</epage><pages>10-15</pages><issn>1006-8104</issn><abstract>The full-length Mlo gene was obtained by reverse transcription polymerase chain reaction (RT-PCR) and RACE. The result of sequence analysis indicated that M/o gene from Pericallis hybrida B. Nord. contained about 1296bp open reading frame and encoded 431 amino acids. According to the comparison of the exogenous gene sequences by BLAST analysis and phylogenetic analysis, Mlo gene shared over 85% nucleotide homology and 98% amino acid homology. Finally, through semi-quantitative-PCR and fluorescence quantitative analysis, we found that Mlo gene showed the highest expression levels in leaves and the lowest in roots after inoculated with powdery mildew pathogen for different days.</abstract></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1006-8104 |
ispartof | 东北农业大学学报:英文版, 2014, Vol.21 (1), p.10-15 |
issn | 1006-8104 |
language | eng |
recordid | cdi_chongqing_primary_48901665 |
source | Alma/SFX Local Collection |
title | Cloning and Expression Analysis of MIo Gene from Pericallis hybrida B. Nord |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T04%3A59%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-chongqing&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cloning%20and%20Expression%20Analysis%20of%20MIo%20Gene%20from%20Pericallis%20hybrida%20B.%20Nord&rft.jtitle=%E4%B8%9C%E5%8C%97%E5%86%9C%E4%B8%9A%E5%A4%A7%E5%AD%A6%E5%AD%A6%E6%8A%A5%EF%BC%9A%E8%8B%B1%E6%96%87%E7%89%88&rft.au=Wang%20Jin-gan%20Li%20Wei%20Ren%20Hong-wei%20Lv%20Yuan-da%20Bai%20Ding%20Xu%20Jing&rft.date=2014&rft.volume=21&rft.issue=1&rft.spage=10&rft.epage=15&rft.pages=10-15&rft.issn=1006-8104&rft_id=info:doi/&rft_dat=%3Cchongqing%3E48901665%3C/chongqing%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_cqvip_id=48901665&rfr_iscdi=true |