龙眼DCL家族基因的启动子分析及时空表达
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国家自然科学基金(31572088,31672127);


Promoter Analysis and Spatial and Temporal Expression of the DCL Family Genes in Dimocarpus longan Lour.
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    摘要:

    为了解龙眼DCL基因的功能,该试验对龙眼基因组数据提取的DlDCL1、DlDCL2、DlDCL3和DlDCL4基因序列进行启动子顺式作用元件及其受miRNA调控的分析;并以龙眼胚性愈伤组织为材料,研究了DlDCLs不同基因成员在非生物胁迫和外源激素处理下的表达情况。结果显示:(1)龙眼DCL基因启动子中除了TATA和CAAT外,还具有大量的光反应元件、激素应答元件、胁迫响应元件、组织特异性调控元件及植物生长发育相关的顺式调控元件,提示龙眼DCL基因启动子转录活性可能受到光、激素信号及逆境胁迫因素的诱导。(2)对调控龙眼DCL基因的miRNA进行筛选,结果显示DlDCL1受miR162和miR1024调控,DlDCL4受miR390和miR396调控。(3)实时荧光定量PCR显示,在一定浓度范围内,外源激素GA3、ABA和ETH 均能下调DlDCLs基因的表达,而高浓度ETH处理则显著上调DlDCLs的表达。(4)高浓度蔗糖(6%)处理时DlDCL2、DlDCL3和DlDCL4显著上调表达,而低浓度(0.1%)处理时DlDCL1显著上调表达;不同温度处理下,DlDCL1在34 ℃时显著上升,DlDCL3随着温度的提高相对表达量逐渐减低;而DlDCL2和DlDCL4表达量差异不明显;NaCl 胁迫处理下,DlDCLs在1 h处理时表达量下调,但在其他不同时间点则上调表达。研究表明,龙眼DCL基因在外源激素及非生物胁迫处理下,并非是简单的一对一响应,而是存在较为复杂的响应机制。

    Abstract:

    In order to investigate the functions of DCL genes in Dimocarpus longan, we isolated gene sequences of DlDCL1, DlDCL2, DlDCL3 and DlDCL4 from D. longan genome data. Analysis of cisacting elements and regulation of miRNA were performed on the DlDCLs family members. Expression of DlDCLs were analyzed in embryogenic callus (EC) under abiotic stress and exogenous hormone treatment in D. longan. The results showed that: (1) the promoters of D. longan DCL genes not only included the cisacting elements of TATA and CAAT box, but also had a large number of light response elements, hormone response elements, stress response elements, tissue specific regulatory elements and other ciselements for plant growth and development. These results suggested that the transcriptional activity of the promoters of D. longan DCL gene might be induced by the signals of light, phytohormones and abiotic stresses. (2) The miRNAs were screened for their effect in regulating D. longan DCL genes, and the results showed that DlDCL1 was regulated by miR162 and miR1024, while DlDCL4 was regulated by miR390 and miR396. (3) The expression of DlDCLs was analyzed by realtime quantitative PCR. It was found that after GA3, ABA and ETH treatments, DlDCLs gene were downregulated. However, they were dramatically upregulated under high concentration of ETH treatment. (4) DlDCL2, DlDCL3 and DlDCL4 were upregulated when they were treated with high concentration of sucrose (6%), in the exception of DlDCL1, which was significantly increased at 0.1% sucrose concentration. During heat treatment, DlDCL1 was significantly upregulated at 34 ℃, whiles the DlDCL3 gradually decreased with rising temperature. The expression level of DlDCL2 and DlDCL4 exhibited slight variations. NaCl treatment induced the response of DlDCLs at different time intervals, however, inhibited the expression of DlDCLs at 1 h. The expression patterns of D. longan DCL genes response to hormones and abiotic stresses suggested that DlDCLs gene were not of a simple one to one correspondence but rather a complex response mechanism.

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陈晓慧,白 玉,李汉生,等.龙眼DCL家族基因的启动子分析及时空表达[J].西北植物学报,2017,37(10):1926-1933

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  • 在线发布日期: 2017-12-01
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