CAJ | 학술논문

通过RNAi策略转化小麦,以降低小麦种子中直链淀粉的含量.小麦中直链淀粉合成的合型淀粉合成酶(Granule-bound starch synthase l,GBSSI,即WAXY蛋白),通过RT-PCR方法从小麦种子中分离出Waxy基因.Southern杂交分析表明,在基因组中存在3个Waxy基因.Northern杂交分析显示出在授粉后的小麦种子中检测到Waxy mRNA.利用RNA沉默策略,将Waxy编码区683 bp的正向和反向片段以及150 bp内含子,连接于表达载体pCAMBIA 3300中玉米ubi1启动子下游.以扬麦10号授粉后15 d的幼胚为外植体,利用农杆菌介导的方法进行转化.通过PCR、RT-PCR和叶片离体褪绿实验鉴定出4株转基因植株.小麦胚乳l2-Kl染色和直链淀粉含量测定表明这4株转基因植株直链淀粉含量明显下降.研究结果表明Waxy基因的RNA沉默使转基因小麦种子直链淀粉的含量下降.
통과RNAi책략전화소맥,이강저소맥충자중직련정분적함량.소맥중직련정분합성적합형정분합성매(Granule-bound starch synthase l,GBSSI,즉WAXY단백),통과RT-PCR방법종소맥충자중분리출Waxy기인.Southern잡교분석표명,재기인조중존재3개Waxy기인.Northern잡교분석현시출재수분후적소맥충자중검측도Waxy mRNA.이용RNA침묵책략,장Waxy편마구683 bp적정향화반향편단이급150 bp내함자,련접우표체재체pCAMBIA 3300중옥미ubi1계동자하유.이양맥10호수분후15 d적유배위외식체,이용농간균개도적방법진행전화.통과PCR、RT-PCR화협편리체퇴록실험감정출4주전기인식주.소맥배유l2-Kl염색화직련정분함량측정표명저4주전기인식주직련정분함량명현하강.연구결과표명Waxy기인적RNA침묵사전기인소맥충자직련정분적함량하강.
In this study,the level of amylose was reduced in wheat seeds by RNAi strategy. Because the synthesis of amylose is catalyzed by the granule-bound starch synthase I ( GBSSI or WAXY protein), the Waxy gene of wheat was isolated from wheat seeds by using RT-PCR. Southern analysis confirmed that there were three Waxy genes in wheat genome. Northern hybridization showed that Waxy mRNA accumulated in seeds following pollination. By RNAi strategy,the 683 bp sense and antisense fragments in reverse orientation separated by a 150 bp intron were cloned into pCAMBIA 3300 just downstream of the maize ubi1 promoter. By Agrobacterium-mediated wheat transformation method, four transgenic plants (Cultivar Yangmai 10) were identified by PCR, RT-PCR and leaf painting assay. The level of amylose in the endosperm were significantly reduced in transgenic seeds as checked by iodine staining and analysis of amylose content. The results indicated that RNAsilencing of Waxy gene resulted in low level of amylose in the seeds of transgenic wheat.