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作 者:宋东光[1] 孙国枫[1] 单海燕[1] 彭翔寅 王光清[1] 汪训明[1] 谈家桢[1]
出 处:《Acta Botanica Sinica》1998年第9期796-802,共7页Acta Botanica Sinica(植物学报:英文版)
摘 要:将0.4、0.8、1.6、2.9kbGBSS基因的5′侧翼区与GUS基因融合,构建了双元表达载体。0.8kbGBSSGUS通过基因枪介导在块茎切片中获得了瞬间表达。以上建构物通过农杆菌介导转入了马铃薯(SolanumtuberosumL.cv.Desiree)。XGluc染色及PCR结果证实已获得转基因植株。利用离体块茎诱导系统,GUS表达用荧光进行定量检测,结果显示,2.9、1.6、0.4kbGBSSGUS的表达均以块茎明显高于茎段,达2~10倍。0.8、1.6、2.9kbGBSSGUS表达高于0.4kbGBSSGUS。蔗糖浓度的升高可诱导GBSSGUS的表达,而光照抑制了GBSSGUS的表达。Binary vectors were constructed by fusing 0.4, 0.8, 1.6, and 2.9 kb 5′ flanking regions of GBSS gene with GUS (β glucuronidase). Transient GUS expression was observed in in vitro tuber slices bombarded with 0.8 kb GBSS GUS construct. These constructs were then transferred into potato ( Solanum tuberosum L. cv. Desiree) via Agrobacterium tumefaciens transformation. Transgenic potato plants were confirmed by X Gluc staining and PCR. Using in vitro tuberization system, GUS expressions were assayed with fluorescence, it was shown that 0.8, 1.6 and 2.9 kb GBSS GUS expressions were higher than 0.4 kb GBSS GUS. 1.6 and 2.9 kb GBSS GUS expressions were about 2 to 10 folds higher in tubers than in stems. In cultured shoots, GBSS GUS expression could be induced by increased sucrose concentration but inhibited by light.
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