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首页> 外文期刊>The Journal of Horticultural Science & Biotechnology >Genome-wide identification and involvement of litchi SPL genes in flowering in response to cold and leaf maturity
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Genome-wide identification and involvement of litchi SPL genes in flowering in response to cold and leaf maturity

机译:荔枝SPL基因在开花中的基因组型鉴定和涉及寒冷叶片成熟的

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Litchi (Litchi chinensis Sonn.) flowers from shoot apical meristems after exposure to prolonged cold differently depending on maturity. The molecular mechanism defining that interaction of cold with maturity is not fully understood. In the present study, potted litchi plants with terminal flushes at mature and turning stage were treated with 60-days of cold. The mature plants, but not the turning plants, were competent to flower, indicating the importance of terminal flush maturity on litchi flowering. This result could be explained by the difference in accumulation of soluble sugars in the apical leaves on terminal flushes. To explore this link, the miR156/SPL (SQUAMOSA-Promoters Binding Protein-like) module, a dominant sugar-mediated flowering regulator, was investigated. Eighteen SPL homologues were identified, 11 of which were up-regulated during the transition from juvenile to adult. Ten LcSPLs were highly expressed in response to cold, but only LcSPL1 and LcSPL2 correlated with the age-dependent flowering in response to cold. Further, 12 LcSPLs, putative targets of LcmiR156, were subjected to transient co-expression assays in tobacco leaves. LcSPL3 and LcSPL10 showed direct binding to the LcFT1 promoter in vitro and in vivo. This trans-activation was verified by yeast one-hybrid (Y1H) assays.
机译:荔枝(Litchi Chinensis Sonn。)从拍摄顶端商品中的花朵拍摄后暴露在曝光后延长冷却,具体取决于成熟度。定义寒冷与成熟度相互作用的分子机制尚不完全理解。在本研究中,患有末端的盆栽荔枝植物在成熟和转动阶段冲洗,用60天冷处理。成熟的植物,但不是转向植物,与花是有能力的,表明终端冲洗成熟度对荔枝开花的重要性。该结果可以通过终端叶片上的顶端叶片中可溶性糖的积累差异来解释。为了探索该链接,研究了MiR156 / SPL(Squamosa-Plieters结合蛋白质样)模块,是主要的糖介导的开花调节剂。鉴定了18个SPL同源物,其中11个在从幼年到成人的过渡期间上调。响应于寒冷,10 LCSPLS高度表达,但只有LCSPL1和LCSPL2与因寒冷而依赖于年龄依赖性开花相关的LCSPL1和LCSPL2。此外,12LCSPLS,LCMIR156的推定靶标在烟叶中进行瞬时共同表达测定。 LCSPL3和LCSPL10在体外和体内显示直接与LCFT1启动子的结合。通过酵母单杂交(Y1H)测定验证该逆激活。

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