植物学报
植物學報
식물학보
ACTA BOTANICA SINICA
2004年
8期
948-954
,共7页
钟瑾%刘树君%马世嵩%杨巍%胡鸢雷%吴锜%林忠平
鐘瑾%劉樹君%馬世嵩%楊巍%鬍鳶雷%吳锜%林忠平
종근%류수군%마세숭%양외%호연뢰%오기%림충평
核基质结合区(MARs)%芪合酶基因%白藜芦醇%川鄂爬山虎%转基因烟草%酵母%HPLC
覈基質結閤區(MARs)%芪閤酶基因%白藜蘆醇%川鄂爬山虎%轉基因煙草%酵母%HPLC
핵기질결합구(MARs)%기합매기인%백려호순%천악파산호%전기인연초%효모%HPLC
matrix attachment regions (MARs)%stilbene synthase gene (STS)%resveratrol%Parthenocissus henryana%transgenic tobacco%yeast%HPLC
采用核基质结合区(MARs)来提高转芪合酶基因(STS)烟草(Nicotianatabacum L.)中白藜芦醇产物的含量.MARs是细胞中能与核基质特异紧密结合的DNA片段,体外结合实验表明克隆自酵母的MARs序列能特异地与烟草核基质结合.芪合酶是白藜芦醇生物合成中的关键酶,用RT-PCR方法从川鄂爬山虎(Parthenocissus henryana(Hemsl.)Diels et Gilg)中克隆了与葡萄芪合酶基因有较高同源性的芪合酶编码区,将其置于CaMV35SΩ强启动子下,分别构建两侧带有MARs及不含MARs序列的表达载体,通过农杆菌介导转化烟草.Northern blot及HPLC等分析表明STS基因已整合至烟草染色体中并正常转录,且表达的外源芪合酶在烟草中可催化其底物合成白藜芦醇产物.与对照相比,MARs的存在使转芪合酶基因烟草中白藜芦醇的含量平均提高了约一倍.MARs在转芪合酶基因植物中的应用也为获得抗病性更强、白藜芦醇含量更高、更保健的转基因果蔬的研究奠定了基础.
採用覈基質結閤區(MARs)來提高轉芪閤酶基因(STS)煙草(Nicotianatabacum L.)中白藜蘆醇產物的含量.MARs是細胞中能與覈基質特異緊密結閤的DNA片段,體外結閤實驗錶明剋隆自酵母的MARs序列能特異地與煙草覈基質結閤.芪閤酶是白藜蘆醇生物閤成中的關鍵酶,用RT-PCR方法從川鄂爬山虎(Parthenocissus henryana(Hemsl.)Diels et Gilg)中剋隆瞭與葡萄芪閤酶基因有較高同源性的芪閤酶編碼區,將其置于CaMV35SΩ彊啟動子下,分彆構建兩側帶有MARs及不含MARs序列的錶達載體,通過農桿菌介導轉化煙草.Northern blot及HPLC等分析錶明STS基因已整閤至煙草染色體中併正常轉錄,且錶達的外源芪閤酶在煙草中可催化其底物閤成白藜蘆醇產物.與對照相比,MARs的存在使轉芪閤酶基因煙草中白藜蘆醇的含量平均提高瞭約一倍.MARs在轉芪閤酶基因植物中的應用也為穫得抗病性更彊、白藜蘆醇含量更高、更保健的轉基因果蔬的研究奠定瞭基礎.
채용핵기질결합구(MARs)래제고전기합매기인(STS)연초(Nicotianatabacum L.)중백려호순산물적함량.MARs시세포중능여핵기질특이긴밀결합적DNA편단,체외결합실험표명극륭자효모적MARs서렬능특이지여연초핵기질결합.기합매시백려호순생물합성중적관건매,용RT-PCR방법종천악파산호(Parthenocissus henryana(Hemsl.)Diels et Gilg)중극륭료여포도기합매기인유교고동원성적기합매편마구,장기치우CaMV35SΩ강계동자하,분별구건량측대유MARs급불함MARs서렬적표체재체,통과농간균개도전화연초.Northern blot급HPLC등분석표명STS기인이정합지연초염색체중병정상전록,차표체적외원기합매재연초중가최화기저물합성백려호순산물.여대조상비,MARs적존재사전기합매기인연초중백려호순적함량평균제고료약일배.MARs재전기합매기인식물중적응용야위획득항병성경강、백려호순함량경고、경보건적전기인과소적연구전정료기출.
Matrix attachment regions (MARs) were used to increase resveratrol production in stilbene synthase (STS) gene-transformed tobacco (Nicotiana tabacum L.) in this study. MARs are DNA sequences that bind to the cell's pertinacious nuclear matrix to form DNA loop domains. A range of effects of MARs sequence on mean expression level and variation in expression of transgenes has been reported usually using β-glucuronidase (GLS) gene as reporter gene. The present study investigated the effects of MARs sequence from yeast on transgene expression of STS for the first time. The results of in vitro binding assay showed that the MARs sequence could specifically bind to the matrix of tobacco prepared by lihium diiodosalicylate (LIS) procedure. The stilbene synthase is the key enzyme in metabolic pathway of resveratrol biosynthesis and a cDNA for STSwas cloned from Parthenocissus henryana (Hemsl.) Diels et Gilg by RTPCR method with primers designed according to the conserved sequence of STSgene in grapevine. The cloned sequence showed high nucleotide identity (93.8%) with the STS gene of Vitis vinifera cv. Optima,and the predicted protein sequence also had Cys164 activity core and IPNSAGAIAGN motifs which were specific for stilbene synthases. With or without flanking MARs from yeast, the STS gene under control of CaMV35S promoter with Ω enhancer has been transferred into tobacco. Northern blot and HPLC analysis of the leaf extracts of transgenic tobacco showed the resveratrol had been produced in STS genetransformed plants, while there was no resveratrol found in the untransformed tobacco. In stably transformed strains, the content of resveratrol in the plants with STSgene flanking by MARs averaged about 2-fold higher than those lacking MARs. The results proved that flanking STS by MARs was one of the effective way to increase resveratrol production in transgenic plants, and this work could also play basic roles on the STS gene transformed vegetables or fruits with strong resistance to disease and benefits to human health.