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盐生杜氏藻烯醇酶基因启动子的克隆分析及胁迫转录应答

DOI: 10.3724/SP.J.1145.2011.00202, PP. 202-206

Keywords: 盐生杜氏藻,烯醇酶,基因组步行,启动子,实时荧光定量pcr,胁迫应答

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Abstract:

为了解盐生杜氏藻(dunaliellasalina)烯醇酶(enolase)在渗透耐受中的具体功能,利用基因组步行方法和巢式pcr,从d.salina中克隆了烯醇酶基因dseno5’上游约2000bp的调控序列,并对其进行序列分析.分析表明,它包含多个与转录调控有关的保守序列(如caat-box,tata-box),富含光?干旱及其它胁迫应答元件.利用实时荧光定量pcr的方法,研究了高渗?高温以及低温外界胁迫条件下dseno的转录情况,发现其受高渗强烈抑制,高温显著诱导而低温微弱诱导.图4表2参19

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