Wang Ya-Jun, Jiang Chao, Zhao Rong, Zhao Le, Shen Ye, Huang Lu-Qi
National Resource Center for Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China.
Zhongguo Zhong Yao Za Zhi. 2013 Jul;38(13):2063-7.
In order to study function of NAC transcription in development, hormone regulation and the stress response of Salvia miltiorrhiza, the NAC transcription was cloned and analyzed. By retrieving cDNA database of S. miltiorrhiza hairy root one NAC unigene was found, then a full length of cDNA was cloned by designing specific primers and PCR amplifying. Using ORF finder it was found that the cDNA containing a NAC-AB conserved domain in N-terminal, so the cDNA was a NAC transcription factor, named as SmNAC1 (kF006346). Bioinformatics analysis showed that SmNAC1 had an open reading frame (ORF) of 591 bp encoding 196 amino acids. The calculated protein had isoelectric point (pI) of 4.36 with molecular weight about 21.66 kDa. The transcription level of SmNAC1 after dealing with yeast extract (YE) and silver ion (Ag+) in S. miltiorrhiza hairy root was markedly stimulated up regulating. It was 1.4 fold compared with the control after induction 2 h, and maintained 2.0 fold on 4-12 h after induction. SmNAC1 may participate in regulation of stress response of YE + Ag+.
为了研究NAC转录在丹参发育、激素调控及胁迫响应中的功能,对NAC转录进行了克隆与分析。通过检索丹参毛状根的cDNA数据库,发现了一个NAC单基因,然后设计特异性引物并通过PCR扩增克隆到了其全长cDNA。利用ORF finder发现该cDNA在N端含有一个NAC-AB保守结构域,因此该cDNA为一个NAC转录因子,命名为SmNAC1(登录号为KF006346)。生物信息学分析表明,SmNAC1的开放阅读框(ORF)为591 bp,编码196个氨基酸。计算得到的蛋白质等电点(pI)为4.36,分子量约为21.66 kDa。在丹参毛状根中用酵母提取物(YE)和银离子(Ag+)处理后,SmNAC1的转录水平显著上调。诱导2 h后与对照相比为1.4倍,诱导后4 - 12 h维持在2.0倍。SmNAC1可能参与YE + Ag+胁迫响应的调控。