Kuipers A G, Soppe W J, Jacobsen E, Visser R G
Department of Plant Breeding, Wageningen Agricultural University, The Netherlands.
Plant Mol Biol. 1994 Dec;26(6):1759-73. doi: 10.1007/BF00019490.
Transgenic plants of a tetraploid potato cultivar were obtained in which the amylose content of tuber starch was reduced via antisense RNA-mediated inhibition of the expression of the gene encoding granule-bound starch synthase (GBSS). GBSS is one of the key enzymes in the biosynthesis of starch and catalyses the formation of amylose. The antisense GBSS genes, based on the full-length GBSS cDNA driven by the 35S CaMV promoter or the potato GBSS promoter, were introduced into the potato genome by Agrobacterium tumefaciens-mediated transformation. Expression of each of these genes resulted in the complete inhibition of GBSS gene expression, and thus in the production of amylose-free tuber starch, in mature field-grown plants originating from rooted in vitro plantlets of 4 out of 66 transgenic clones. Clones in which the GBSS gene expression was incompletely inhibited showed an increase of the extent of inhibition during tuber growth. This is likely to be due to the increase of starch granule size during tuber growth and the specific distribution pattern of starch components in granules of clones with reduced GBSS activity. Expression of the antisense GBSS gene from the GBSS promoter resulted in a higher stability of inhibition in tubers of field-grown plants as compared to expression from the 35S CaMV promoter. Field analysis of the transgenic clones indicated that inhibition of GBSS gene expression could be achieved without significantly affecting the starch and sugar content of transgenic tubers, the expression level of other genes involved in starch and tuber metabolism and agronomic characteristics such as yield and dry matter content.
通过反义RNA介导抑制编码颗粒结合淀粉合酶(GBSS)的基因表达,获得了四倍体马铃薯品种的转基因植株,其块茎淀粉的直链淀粉含量降低。GBSS是淀粉生物合成中的关键酶之一,催化直链淀粉的形成。基于由35S CaMV启动子或马铃薯GBSS启动子驱动的全长GBSS cDNA的反义GBSS基因,通过根癌农杆菌介导的转化被导入马铃薯基因组。这些基因中的每一个的表达导致GBSS基因表达的完全抑制,从而在源自66个转基因克隆中的4个的体外生根苗的成熟田间生长植株中产生无直链淀粉的块茎淀粉。GBSS基因表达未被完全抑制的克隆在块茎生长期间显示出抑制程度的增加。这可能是由于块茎生长期间淀粉颗粒大小的增加以及GBSS活性降低的克隆的颗粒中淀粉成分的特定分布模式。与来自35S CaMV启动子的表达相比,来自GBSS启动子的反义GBSS基因的表达在田间生长植株的块茎中导致更高的抑制稳定性。对转基因克隆的田间分析表明,抑制GBSS基因表达可以在不显著影响转基因块茎的淀粉和糖含量、参与淀粉和块茎代谢的其他基因的表达水平以及诸如产量和干物质含量等农艺性状的情况下实现。