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Transgenic Bt cotton driven by the green tissue-specific promoter shows strong toxicity to lepidopteran pests and lower Bt toxin accumulation in seeds
A promoter of the PNZIP (Pharbitis nil leucine zipper) gene (1.459 kb) was cloned from Pharbitis nil and fused to the GUS(~-glucuronidase) and Bacillus thuringiensis endotoxin (Cry9C) genes. Several transgenic PNZIP::GUS and PNZIP::Cry9C cotton lines were developed by Agrobacterium-mediated transfor...
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Published in: | Science China. Life sciences 2016-02, Vol.59 (2), p.172-182 |
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description | A promoter of the PNZIP (Pharbitis nil leucine zipper) gene (1.459 kb) was cloned from Pharbitis nil and fused to the GUS(~-glucuronidase) and Bacillus thuringiensis endotoxin (Cry9C) genes. Several transgenic PNZIP::GUS and PNZIP::Cry9C cotton lines were developed by Agrobacterium-mediated transformation. Strong GUS staining was detected in the green tissues of the transgenic PNZIP::GUS cotton plants. In contrast, GUS staining in the reproductive structures such as petals, anther, and immature seeds of PNZIP::GUS cotton was very faint. Two transgenic PNZIP::Cry9C lines and one trans- genic cauliflower mosaic virus (CaMV) 35S::Cry9C line were selected for enzyme-linked immunosorbent assay (ELISA) and insect bioassays. Expression of the Cry9C protein in the 35S::Cry9C line maintained a high level in most tissues ranging from 24.6 to 45.5 ~tg g-I fresh weight. In green tissues such as the leaves, boll rinds, and bracts of the PNZIP::Cry9C line, the Cry9C protein accumulated up to 50.2, 39.7, and 48.3 jag g-a fresh weight respectively. In contrast, seeds of the PNZIP::Cry9C line (PZ1.3) accumulated only 0.26 ~ag g-~ fresh weight of the Cry9C protein, which was 100 times lower than that recorded for the seeds of the CaMV 35S::Cry9C line. The insect bioassay showed that the transgenic PNZIP::Cry9C cotton plant exhibited strong resistance to both the cotton bollworm and the pink bollworm. The PNZIP promoter could effectively drive Bt toxin ex- pression in green tissues of cotton and lower accumulated levels of the Bt protein in seeds. These features should allay public concerns about the safety of transgenic foods. We propose the future utility of PNZIP as an economical, environmentally friendly promoter in cotton biotechnology. |
doi_str_mv | 10.1007/s11427-015-4920-6 |
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Several transgenic PNZIP::GUS and PNZIP::Cry9C cotton lines were developed by Agrobacterium-mediated transformation. Strong GUS staining was detected in the green tissues of the transgenic PNZIP::GUS cotton plants. In contrast, GUS staining in the reproductive structures such as petals, anther, and immature seeds of PNZIP::GUS cotton was very faint. Two transgenic PNZIP::Cry9C lines and one trans- genic cauliflower mosaic virus (CaMV) 35S::Cry9C line were selected for enzyme-linked immunosorbent assay (ELISA) and insect bioassays. Expression of the Cry9C protein in the 35S::Cry9C line maintained a high level in most tissues ranging from 24.6 to 45.5 ~tg g-I fresh weight. In green tissues such as the leaves, boll rinds, and bracts of the PNZIP::Cry9C line, the Cry9C protein accumulated up to 50.2, 39.7, and 48.3 jag g-a fresh weight respectively. In contrast, seeds of the PNZIP::Cry9C line (PZ1.3) accumulated only 0.26 ~ag g-~ fresh weight of the Cry9C protein, which was 100 times lower than that recorded for the seeds of the CaMV 35S::Cry9C line. The insect bioassay showed that the transgenic PNZIP::Cry9C cotton plant exhibited strong resistance to both the cotton bollworm and the pink bollworm. The PNZIP promoter could effectively drive Bt toxin ex- pression in green tissues of cotton and lower accumulated levels of the Bt protein in seeds. These features should allay public concerns about the safety of transgenic foods. We propose the future utility of PNZIP as an economical, environmentally friendly promoter in cotton biotechnology.</description><identifier>ISSN: 1674-7305</identifier><identifier>EISSN: 1869-1889</identifier><identifier>DOI: 10.1007/s11427-015-4920-6</identifier><identifier>PMID: 26728504</identifier><language>eng</language><publisher>Beijing: Science China Press</publisher><subject>35S启动子 ; Animals ; Bacillus thuringiensis - genetics ; Bacterial Proteins - metabolism ; Biomedical and Life Sciences ; Bt毒素 ; Endotoxins - metabolism ; Gossypium - genetics ; Hemolysin Proteins - metabolism ; Lepidoptera - pathogenicity ; Life Sciences ; Plants, Genetically Modified ; Promoter Regions, Genetic ; Research Paper ; Seeds - metabolism ; 特异性启动子 ; 种子 ; 绿色组织 ; 转Bt基因抗虫棉 ; 驱动 ; 鳞翅目害虫</subject><ispartof>Science China. Life sciences, 2016-02, Vol.59 (2), p.172-182</ispartof><rights>The Author(s) 2015</rights><rights>Science in China Press and Springer-Verlag GmbH 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c545t-9e37660cffcc82aa3713b6829102dc603288e698928afedd0e1eef7deb278e5f3</citedby><cites>FETCH-LOGICAL-c545t-9e37660cffcc82aa3713b6829102dc603288e698928afedd0e1eef7deb278e5f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/60112X/60112X.jpg</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26728504$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Qing</creatorcontrib><creatorcontrib>Zhu, Yi</creatorcontrib><creatorcontrib>Sun, Lin</creatorcontrib><creatorcontrib>Li, Lebin</creatorcontrib><creatorcontrib>Jin, Shuangxia</creatorcontrib><creatorcontrib>Zhang, Xianlong</creatorcontrib><title>Transgenic Bt cotton driven by the green tissue-specific promoter shows strong toxicity to lepidopteran pests and lower Bt toxin accumulation in seeds</title><title>Science China. Life sciences</title><addtitle>Sci. China Life Sci</addtitle><addtitle>Sci China Life Sci</addtitle><description>A promoter of the PNZIP (Pharbitis nil leucine zipper) gene (1.459 kb) was cloned from Pharbitis nil and fused to the GUS(~-glucuronidase) and Bacillus thuringiensis endotoxin (Cry9C) genes. Several transgenic PNZIP::GUS and PNZIP::Cry9C cotton lines were developed by Agrobacterium-mediated transformation. Strong GUS staining was detected in the green tissues of the transgenic PNZIP::GUS cotton plants. In contrast, GUS staining in the reproductive structures such as petals, anther, and immature seeds of PNZIP::GUS cotton was very faint. Two transgenic PNZIP::Cry9C lines and one trans- genic cauliflower mosaic virus (CaMV) 35S::Cry9C line were selected for enzyme-linked immunosorbent assay (ELISA) and insect bioassays. Expression of the Cry9C protein in the 35S::Cry9C line maintained a high level in most tissues ranging from 24.6 to 45.5 ~tg g-I fresh weight. In green tissues such as the leaves, boll rinds, and bracts of the PNZIP::Cry9C line, the Cry9C protein accumulated up to 50.2, 39.7, and 48.3 jag g-a fresh weight respectively. In contrast, seeds of the PNZIP::Cry9C line (PZ1.3) accumulated only 0.26 ~ag g-~ fresh weight of the Cry9C protein, which was 100 times lower than that recorded for the seeds of the CaMV 35S::Cry9C line. The insect bioassay showed that the transgenic PNZIP::Cry9C cotton plant exhibited strong resistance to both the cotton bollworm and the pink bollworm. The PNZIP promoter could effectively drive Bt toxin ex- pression in green tissues of cotton and lower accumulated levels of the Bt protein in seeds. These features should allay public concerns about the safety of transgenic foods. We propose the future utility of PNZIP as an economical, environmentally friendly promoter in cotton biotechnology.</description><subject>35S启动子</subject><subject>Animals</subject><subject>Bacillus thuringiensis - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Biomedical and Life Sciences</subject><subject>Bt毒素</subject><subject>Endotoxins - metabolism</subject><subject>Gossypium - genetics</subject><subject>Hemolysin Proteins - metabolism</subject><subject>Lepidoptera - pathogenicity</subject><subject>Life Sciences</subject><subject>Plants, Genetically Modified</subject><subject>Promoter Regions, Genetic</subject><subject>Research Paper</subject><subject>Seeds - metabolism</subject><subject>特异性启动子</subject><subject>种子</subject><subject>绿色组织</subject><subject>转Bt基因抗虫棉</subject><subject>驱动</subject><subject>鳞翅目害虫</subject><issn>1674-7305</issn><issn>1869-1889</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp9kc1u1DAUhS0EotXQB2CDLNiwCfgnsZ0lVPxJldiUteVxbmZcJXZqO7R9EZ6XO5qhQizwxrb8nXOv7yHkJWfvOGP6feG8FbphvGvaXrBGPSHn3Ki-4cb0T_GsdNtoybozclHKDcMlJRNaPydnQmlhOtaek1_X2cWygxg8_VipT7WmSIccfkKk2wda90B3GfBSQykrNGUBH0akl5zmVCHTsk93hZaaU9zRmu6DDxWFiU6whCEtyLhIFyi1UBcHOqU7VGGxAxup836d18nVgIXxXgCG8oI8G91U4OK0b8iPz5-uL782V9-_fLv8cNX4ru1q04PUSjE_jt4b4ZzUXG6VET1nYvCKSWEMqN70wrgRhoEBBxj1AFuhDXSj3JC3R1_8ze2KLdo5FA_T5CKktVhucFDSaBzdhrz5B71Ja47YneVacYWTlR1S_Ej5nErJMNolh9nlB8uZPeRmj7lZzM0ecrMKNa9Ozut2huFR8SclBMQRKPgUd5D_Kv0f19enTvYYzC3qHo2V0sZo3vbyN1pmsTk</recordid><startdate>20160201</startdate><enddate>20160201</enddate><creator>Wang, Qing</creator><creator>Zhu, Yi</creator><creator>Sun, Lin</creator><creator>Li, Lebin</creator><creator>Jin, Shuangxia</creator><creator>Zhang, Xianlong</creator><general>Science China Press</general><general>Springer Nature B.V</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>~WA</scope><scope>C6C</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>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</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>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>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20160201</creationdate><title>Transgenic Bt cotton driven by the green tissue-specific promoter shows strong toxicity to lepidopteran pests and lower Bt toxin accumulation in seeds</title><author>Wang, Qing ; 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Life sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Qing</au><au>Zhu, Yi</au><au>Sun, Lin</au><au>Li, Lebin</au><au>Jin, Shuangxia</au><au>Zhang, Xianlong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transgenic Bt cotton driven by the green tissue-specific promoter shows strong toxicity to lepidopteran pests and lower Bt toxin accumulation in seeds</atitle><jtitle>Science China. Life sciences</jtitle><stitle>Sci. China Life Sci</stitle><addtitle>Sci China Life Sci</addtitle><date>2016-02-01</date><risdate>2016</risdate><volume>59</volume><issue>2</issue><spage>172</spage><epage>182</epage><pages>172-182</pages><issn>1674-7305</issn><eissn>1869-1889</eissn><abstract>A promoter of the PNZIP (Pharbitis nil leucine zipper) gene (1.459 kb) was cloned from Pharbitis nil and fused to the GUS(~-glucuronidase) and Bacillus thuringiensis endotoxin (Cry9C) genes. Several transgenic PNZIP::GUS and PNZIP::Cry9C cotton lines were developed by Agrobacterium-mediated transformation. Strong GUS staining was detected in the green tissues of the transgenic PNZIP::GUS cotton plants. In contrast, GUS staining in the reproductive structures such as petals, anther, and immature seeds of PNZIP::GUS cotton was very faint. Two transgenic PNZIP::Cry9C lines and one trans- genic cauliflower mosaic virus (CaMV) 35S::Cry9C line were selected for enzyme-linked immunosorbent assay (ELISA) and insect bioassays. Expression of the Cry9C protein in the 35S::Cry9C line maintained a high level in most tissues ranging from 24.6 to 45.5 ~tg g-I fresh weight. In green tissues such as the leaves, boll rinds, and bracts of the PNZIP::Cry9C line, the Cry9C protein accumulated up to 50.2, 39.7, and 48.3 jag g-a fresh weight respectively. In contrast, seeds of the PNZIP::Cry9C line (PZ1.3) accumulated only 0.26 ~ag g-~ fresh weight of the Cry9C protein, which was 100 times lower than that recorded for the seeds of the CaMV 35S::Cry9C line. The insect bioassay showed that the transgenic PNZIP::Cry9C cotton plant exhibited strong resistance to both the cotton bollworm and the pink bollworm. The PNZIP promoter could effectively drive Bt toxin ex- pression in green tissues of cotton and lower accumulated levels of the Bt protein in seeds. These features should allay public concerns about the safety of transgenic foods. We propose the future utility of PNZIP as an economical, environmentally friendly promoter in cotton biotechnology.</abstract><cop>Beijing</cop><pub>Science China Press</pub><pmid>26728504</pmid><doi>10.1007/s11427-015-4920-6</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 35S启动子 Animals Bacillus thuringiensis - genetics Bacterial Proteins - metabolism Biomedical and Life Sciences Bt毒素 Endotoxins - metabolism Gossypium - genetics Hemolysin Proteins - metabolism Lepidoptera - pathogenicity Life Sciences Plants, Genetically Modified Promoter Regions, Genetic Research Paper Seeds - metabolism 特异性启动子 种子 绿色组织 转Bt基因抗虫棉 驱动 鳞翅目害虫 |
title | Transgenic Bt cotton driven by the green tissue-specific promoter shows strong toxicity to lepidopteran pests and lower Bt toxin accumulation in seeds |
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