Dugdale B, Beetham P R, Becker D K, Harding R M, Dale J L
Centre for Molecular Biotechnology, School of Life Sciences, Queensland University of Technology, Brisbane, Australia.
J Gen Virol. 1998 Oct;79 ( Pt 10):2301-11. doi: 10.1099/0022-1317-79-10-2301.
Promoter regions associated with each of the six ssDNA components of banana bunchy top virus (BBTV) have been characterized. DNA segments incorporating the intergenic regions of BBTV DNA-1 to -6 were isolated and fused to the uidA (beta-glucuronidase) reporter gene to assess promoter activity. In tobacco cell suspensions, the BBTV DNA-2 and -6 promoters generated levels of GUS expression 2-fold greater and similar to the 800 bp CaMV 35S promoter, respectively. Deletion analysis of the BBTV DNA-6 promoter suggested all the necessary promoter elements required for strong expression were located within 239 nucleotides upstream of the translational start codon. In transgenic tobacco plants, the BBTV-derived promoters generally provided a weak, tissue-specific GUS expression pattern restricted to phloem-associated cells. However, in callus derived from tobacco leaf tissue, GUS expression directed by the BBTV DNA-6 promoter was strong and, in some lines, comparable to the CaMV 35S promoter. Detectable promoter activity associated with the BBTV promoters in banana embryogenic cells was only observed using a sensitive green fluorescent protein (GFP) reporter. Promoters derived from BBTV DNA-4 and -5 generated the highest levels of transient activity, which were greater than that of the maize ubi-1 promoter. In transgenic banana plants, the activity of the BBTV DNA-6 promoter was restricted to the phloem of leaves and roots, stomata and root meristems.
已对与香蕉束顶病毒(BBTV)的六个单链DNA组分相关的启动子区域进行了表征。分离出包含BBTV DNA - 1至 - 6基因间隔区的DNA片段,并将其与uidA(β - 葡萄糖醛酸酶)报告基因融合,以评估启动子活性。在烟草细胞悬浮液中,BBTV DNA - 2和 - 6启动子分别产生的GUS表达水平比800 bp CaMV 35S启动子高2倍和与之相似。对BBTV DNA - 6启动子的缺失分析表明,强表达所需的所有必要启动子元件都位于翻译起始密码子上游239个核苷酸内。在转基因烟草植株中,源自BBTV的启动子通常提供一种弱的、组织特异性的GUS表达模式,仅限于与韧皮部相关的细胞。然而,在源自烟草叶组织的愈伤组织中,由BBTV DNA - 6启动子指导的GUS表达很强,并且在某些株系中与CaMV 35S启动子相当。仅使用敏感的绿色荧光蛋白(GFP)报告基因才观察到香蕉胚性细胞中与BBTV启动子相关的可检测启动子活性。源自BBTV DNA - 4和 - 5的启动子产生的瞬时活性水平最高,高于玉米ubi - 1启动子。在转基因香蕉植株中,BBTV DNA - 6启动子的活性仅限于叶和根的韧皮部、气孔和根分生组织。