Wu Han Ying, Liu Jing Mei, Zhu Zhu Jun, Yang Xin Ting, Chen Da Ming
Department of Horticulture, Zhejiang University, Hangzhou 310029, China.
Shi Yan Sheng Wu Xue Bao. 2003 Jun;36(3):226-32.
According to its restriction sites, fragments of 1573 bp, 1197 bp, 896 bp and 795 bp were obtained from the 5' promoter region of wml1 and fused with the coding sequence of the GUS gene. Constructs containing these fragments were introduced into tomato plants via Agrobacterium-mediated transformation. Histochemical assay of GUS expression in transgenic tomato plants revealed that fragments of 1573 bp, 1197 bp, 896 bp were able to direct GUS expression in fruits of 15, 30, 45 days after anthesis with the expression level of GUS increasing with fruit development, but not in leaves, stems and roots. While no GUS expression was observed in tomato plants transformed by construct containing fragment of 795 bp. It was determined that the region from 857 bp to 957 bp contains the elements necessary for directing fruit-specific expression.
根据其限制性酶切位点,从wml1的5'启动子区域获得了1573 bp、1197 bp、896 bp和795 bp的片段,并将其与GUS基因的编码序列融合。通过农杆菌介导的转化将含有这些片段的构建体导入番茄植株。对转基因番茄植株中GUS表达的组织化学分析表明,1573 bp、1197 bp、896 bp的片段能够在开花后15、30、45天的果实中指导GUS表达,且GUS表达水平随果实发育而增加,但在叶片、茎和根中不表达。而在含有795 bp片段的构建体转化的番茄植株中未观察到GUS表达。确定857 bp至957 bp的区域包含指导果实特异性表达所需的元件。