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Characterization and transcriptional regulation of chlorophyll b reductase gene NON-YELLOW COLORING 1 associated with leaf senescence in perennial ryegrass (Lolium perenne L.)

机译:叶绿素B叶片叶绿素黑麦叶衰老叶绿素B还原酶基因1的表征及转录调控(Lolium Perenne L.)

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Chlorophyll (Chl) degradation leads to leaf senescence and adversely affects biomass production of forage grasses and aesthetic appearance of turfgrasses. The objectives of this study were to characterize the function of a Chl catabolic gene, NON-YELLOW COLORING 1 (LpNYC1), and to understand its transcriptional regulatory pattern involved in leaf senescence in perennial ryegrass (Lolium perenne L.) The LpNYC1 was initially cloned using the RACE-PCR method. Its encoded protein was localized in chloroplasts and its expression pattern was correlated with the progression of leaf senescence. LpNYC1 shared the same biological function with Arabidopsis NYC1, as overexpression of its encoding gene accelerated chlorophyll degradation in Nicotiana benthamiana and rescued the stay-green phenotype of the Arabidopsis nyc1 null mutant. A yeast one-hybrid cDNA library was prepared from senescent leaves of perennial ryegrass. Using the LpNYC1 promoter as bait, five putative transcription factors upstream of LpNYC1 were pooled out using this method, among which three (LpABI5, LpABF3, and LpEIN3) were orthologous to Arabidopsis transcription factors involved in the ABA and ethylene signaling pathways. The expression of LpNYC1 was highly inducible by ABA and ethephon (ethylene releasing reagent) but was suppressed by treatment with AVG (ethylene biosynthesis inhibitor). Furthermore, LpABI5, LpABF3, LpEIN3 directly activated the expression of LpNYC1 by binding to its promoter. The current result laid the groundwork for future in-depth analysis of the molecular regulation of LpNYC1 and Chl metabolism during leaf senescence in perennial grass species.
机译:叶绿素(CHL)降解导致叶片衰老,并且对草坪草的饲料草和美学外观产生不利影响。本研究的目标是表征CHL分解代谢基因,非黄色着色1(LPNYC1)的功能,并了解涉及叶片衰老的转录调节模式在多年生黑麦草(Lolium Perenne L.)中最初克隆LPNYC1使用RACE-PCR方法。其编码的蛋白质在叶绿体中局部化,其表达模式与叶片衰老的进展相关。 LPNYC1与Arabidopsis NYC1共享相同的生物学功能,因为其编码基因的过度表达加速了尼古拉·南·南部果白植物中的叶绿素降解,并拯救了拟南芥NYC1空突变体的温度绿色表型。酵母单杂交cDNA文库由多年生黑麦草的衰老叶制备。使用LPNYC1启动子作为诱饵,使用该方法将LPNYC1上游的五个推定转录因子汇集,其中三(LPABI5,LPABF3和LPEIN3)与参与ABA和乙烯信号传导途径的拟南芥转录因子是直观的。 LPNYC1的表达由ABA和Ethephon(乙烯释放试剂)高度诱导,但通过用AVG(乙烯生物合成抑制剂)进行抑制。此外,LPABI5,LPABF3,LPEIN3通过与其启动子结合而直接激活LPNYC1的表达。目前的结果为未来深入分析LPNYC1和CHL代谢在多年生草种中的叶片衰老期间的未来深入分析的基础。

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