Seymour G B, Fray R G, Hill P, Tucker G A
Department of Applied Biochemistry, University of Nottingham, School of Agriculture, Loughborough, Leics, UK.
Plant Mol Biol. 1993 Oct;23(1):1-9. doi: 10.1007/BF00021414.
Tomatoes (Lycopersicon esculentum Mill cv. Ailsa Craig) were transformed with a gene construct having 244 bp of the 5' end of a polygalacturonase (PG) cDNA, coding for a 71 amino acid N-terminal extension to the mature protein, fused to 1320 bp of a pectin-esterase (PE) cDNA encoding the full sequence of the mature PE protein. This chimaeric gene was inserted in a sense orientation between a CaMV 35S promoter and terminator for constitutive expression. In transformed tomato plants expression of the endogenous PG and PE genes in the fruit was inhibited; there was little or no observable PG and PE mRNA and a substantial reduction in the level of PG and PE enzyme activity. The transgene was expressed in the leaves of the transformed plants as demonstrated by the accumulation of mRNA, but no protein product could be identified. However, no transgene mRNA or protein were observed in the transgenic fruit. The paper represents the first report of the down-regulation of two non-homologous endogenous genes using a single gene construct. A sense gene construct was responsible for these effects. These findings are discussed in relation to possible mechanisms of action of co-suppression.
用一个基因构建体转化番茄(Lycopersicon esculentum Mill cv. Ailsa Craig),该构建体含有多聚半乳糖醛酸酶(PG)cDNA 5'端的244 bp,编码成熟蛋白N端的71个氨基酸延伸序列,并与编码成熟果胶酯酶(PE)蛋白全序列的1320 bp的果胶酯酶(PE)cDNA融合。这个嵌合基因以正义方向插入到花椰菜花叶病毒35S启动子和终止子之间以进行组成型表达。在转基因番茄植株中,果实中内源性PG和PE基因的表达受到抑制;几乎没有或没有可观察到的PG和PE mRNA,并且PG和PE酶活性水平大幅降低。转基因在转基因植株的叶片中表达,这通过mRNA的积累得以证明,但未鉴定出蛋白质产物。然而,在转基因果实中未观察到转基因mRNA或蛋白质。该论文是关于使用单个基因构建体下调两个非同源内源性基因的首次报道。一个正义基因构建体导致了这些效应。结合共抑制的可能作用机制对这些发现进行了讨论。