高级检索

    普通烟草WDR 基因的克隆与序列分析

    Cloning and Sequence Analysis of a WDR Gene from Common Tobacco

    • 摘要: 在烟草腺毛的发育中,WD40-bHLH-MYB 复合体起着重要的调控作用。利用RT-PCR 从云烟85 中克隆得到一条普通烟草(Nicotiana tobacum)WDR(NtWDR)全长cDNA 序列,GeneBank 登录号为GQ260131。NtWDR 基因cDNA 全长1 433 bp,具有一个1 029 bp 的开放阅读框(ORF)、一个147 bp 的5′非翻译区和一个257 bp 的3′非翻译区。该基因编码一个342 aa 的蛋白质,预测的分子量为38.49 kDa,等电点为4.81。BLASTs 和NCBI 保守域收索表明,NtWDR 是AN11/TTG1型WD40 蛋白。系统进化和结构特征分析表明,NtWDR 基因是PhAN11 和Le113964R 基因的垂直同源基因。

       

      Abstract: MYB-bHLH-WD40 protein complex plays a crucial role in regulating the trichome differentiation in the tobacco (Nicotiana tabacum). By using RT-PCR method, a WDR (NtWDR) gene was isolated from common tobacco Yuyan 85 and the gene accession number is GQ260131. NtWDR cDNA is 1 433 bp in length with a 1 029 bp open reading frame (ORF) as well as a 147 bp 5′-untranslated region (UTR) and a 257 bp 3′-UTR. The encoded NtWDR protein is 342 aa with a calculated molecular weight (Mw) of 38.49 kDa and a isoelectric point (pI) value of 4.81. BLASTs and NCBI conserved domain search indicated that NtWDR was AN11/TTG1-type WD40 proteins. Phylogenetics analysis and structural characterizations identified NtWDR to be orthologs of PhAN11 and Le113964R.

       

    /

    返回文章
    返回