种子中特异表达IPT基因的植物双元载体构建及转基因水稻获得  

The Construction of a Vector for Endosperm-specific Expression of IPT Gene and It's Transformation in Rice

作　　者：张红心[1,2] 王桂兰[1] 陈超[1] 赵璞[3] 马春红[3] 

机构地区：[1]唐山师范学院生命科学系,河北唐山063000 [2]厦门大学生命科学学院,福建厦门361005 [3]河北省农林科学院遗传生理研究所,河北省植物转基因中心,河北石家庄050051

出　　处：《华北农学报》2015年第1期61-65,共5页Acta Agriculturae Boreali-Sinica

基　　金：唐山师范学院博士基金项目(09A01);农业部“948”项目(2011-G1(3)-07);河北省科技计划项目(13396401D)

摘　　要：为研究细胞分裂素在水稻籽粒发育中的作用,构建了p1300-p PG-5α-IPT-Nos植物表达载体,并对水稻进行遗传转化。以水稻品种9311为材料,采用PCR法获得种子中特异表达的PG-5α基因启动子,并将此启动子与p1300相连接,构建p1300-p PG-5α载体,用NcoⅠ和SpeⅠ双酶切p SG516,获得IPT-Nos核酸片段,然后将此核酸片段插入到p1300-p PG-5α中,构建p1300-p PG-5α-IPT-Nos植物表达载体。以水稻品种日本晴愈伤组织为材料,采用农杆菌介导的方法进行遗传转化。成功构建了植物表达载体p1300-p PG-5α-IPT-Nos,获得了阳性率为81.3%转IPT基因群体。获得转基因株系后,将为进一步筛选高效表达株系及观察其籽粒生长发育过程提供基础。In order to specifically express IPT gene in the endosperm of developing rice seed ,the binary vector p1300-pPG-5α-IPT-Nos was constructed,firstly,the promoter of PG-5αwas obtained by PCR amplification from rice genomic DNA（variety：9311）and p1300-pPG-5αwas constructed by inserting pPG-5αinto p1300,then the IPT-Nos fragment was obtained by cutting pSG 516 with NcoⅠ and SpeⅠ.After IPT-Nos inserted into p1300-pPG-5α, p1300-pPG-5α-IPT-Nos was constructed .pPG-5α-IPT-Nos was transformated into Oryza sativa （ subsp .japonicacv . Nipponbare ） cells by agrobacterium mediated method and regenerative seedlings were obtained .The results of PCR showed that about 81 .3%seedlings were positive .

关 键 词：PG-5α启动子 IPT p1300-pPG-5α-IPT-Nos 水稻 遗传转化 

分 类 号：Q78[生物学—分子生物学]