菊花DgCCD7启动子克隆与顺式作用元件分析
Isolation and cis-element analysis of DgCCD7 promoter in chrysanthemums
本研究以切花菊'神马'(Dendronthema grandiform cv. Jinba)为材料,对菊花Strigolactones合成基因DgCCD7基因启动子的克隆,获得DgCCD7基因启动子1442bp;分别对菊花Strigolactones合成基因DgCCD7与DgCCD8的启动子序列利用数据库(PLACE)分别进行分析,并对两者上游1200bp内的顺势作用元件进行比对分析,发现两个基因均含有两个共同的生长素相关元件:生长素响应元件CATATGGMSAUR以及类生长素响应元件SEBFCONSSTPR10A;除此之外,在两个启动子共同含有的元件中,均具有一个P1Bs结合位点,分别位于ProDgCCD7的-610bp和ProDgCCD8的-427bp,该位点参与响应磷胁迫相关转录因子PHR1的结合;通过转染拟南芥GUS染色结果也可看到DgCCD7在下胚轴以及分生组织染色较深,其根部的GUS表达受到NAA与缺磷的诱导。这一结果为进一步研究基因DgCCD7与DgCCD8的转录调控机制奠定基础,以期揭示strigolactone对菊花侧枝发育的调控机理,为进一步利用人工合成的SL调控菊花侧枝生长特性或通过基因工程手段培育理想株型的切花菊品种提供理论和实践基础。
Strigolactone is known as a long-distance signal in regulation of chrysanthemum shoot branching. The promoter of SL biosynthesis gene, DgCCD7, was isolated from chrysanthemum (Dendranthema grandiflorum cv. Jinba), which contains full-length of 1442bp. By using PLACE database, analysis of promoter sequence of DgCCD7 was carried out. Associated with DgCCD8 promoter, common motifs were identified. Two auxin responsive motifs and one PIBs binding motif were identified on both DgCCD7 and DgCCD8 promoters. By transformation of Arabidopsis fusion with GUS gene, DgCCD7 promoter can be activated at meristems and hypocotyledonary region. Meanwhile NAA and Pi starvation can active GUS expression in roots of transgene Arabidopsis. To sum up, this study can pave the great way for regulation mechanism research in chrysanthemum shoot branching, which can be used for controlling branching during cut flower production..
郗琳、杨云燕、聂静、吕素慧、赵梁军、温超
分子生物学植物学
园艺菊花分枝启动子s独脚金内酯转录调控
HoticultureChrysanthemumShoot branchingPromoterCCDsStrigolactoneTranscription regulation
郗琳,杨云燕,聂静,吕素慧,赵梁军,温超.菊花DgCCD7启动子克隆与顺式作用元件分析[EB/OL].(2016-03-08)[2025-08-11].http://www.paper.edu.cn/releasepaper/content/201603-86.点此复制
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