Gidoni D, Fuss E, Burbidge A, Speckmann G J, James S, Nijkamp D, Mett A, Feiler J, Smoker M, de Vroomen M J, Leader D, Liharska T, Groenendijk J, Coppoolse E, Smit J J M, Levin I, de Both M, Schuch W, Jones J D G, Taylor I B, Theres K, van Haaren M J J
Department of Plant Genetics, Institute of Field Crops, The Volcani Center, PO. Box 6, Bet Dagan 50250, Israel.
Plant Mol Biol. 2003 Jan;51(1):83-98. doi: 10.1023/a:1020718520618.
In order to make the tomato genome more accessible for molecular analysis and gene cloning, we have produced 405 individual tomato (Lycopersicon esculentum) lines containing a characterized copy of pJasm13, a multifunctional T-DNA/modified Ds transposon element construct. Both the T-DNA and the Ds element in pJasm13 harbor a set of selectable marker genes to monitor excision and reintegration of Ds and additionally, target sequences for rare cutting restriction enzymes (I-PpoI, SfiI, NotI) and for site-specific recombinases (Cre, FLP, R). Blast analysis of flanking genomic sequences of 174 T-DNA inserts revealed homology to transcribed genes in 69 (40%), of which about half are known or putatively identified as genes and ESTs. The map position of 140 individual inserts was determined on the molecular genetic map of tomato. These inserts are distributed over the 12 chromosomes of tomato, allowing targeted and non-targeted transposon tagging, marking of closely linked genes of interest and induction of chromosomal rearrangements including translocations or creation of saturation-deletions or inversions within defined regions linked to the T-DNA insertion site. The different features of pJasm13 were successfully tested in tomato and Arabidopsis thaliana, thus providing a new tool for molecular/genetic dissection studies, including molecular and physical mapping, mutation analysis and cloning strategies in tomato and potentially, in other plants as well.
为了使番茄基因组更便于进行分子分析和基因克隆,我们构建了405个独立的番茄(Lycopersicon esculentum)株系,这些株系含有pJasm13的一个特征性拷贝,pJasm13是一种多功能T-DNA/修饰的Ds转座子元件构建体。pJasm13中的T-DNA和Ds元件都带有一组选择标记基因,用于监测Ds的切除和重新整合,此外还带有稀有切割限制酶(I-PpoI、SfiI、NotI)和位点特异性重组酶(Cre、FLP、R)的靶序列。对174个T-DNA插入侧翼基因组序列的Blast分析显示,其中69个(40%)与转录基因具有同源性,其中约一半已知或被推定为基因和EST。在番茄分子遗传图谱上确定了140个独立插入位点的图谱位置。这些插入位点分布在番茄的12条染色体上,可用于靶向和非靶向转座子标签、标记感兴趣的紧密连锁基因以及诱导染色体重排,包括易位或在与T-DNA插入位点相连的特定区域内产生饱和缺失或倒位。pJasm13的不同特性已在番茄和拟南芥中成功测试,从而为分子/遗传剖析研究提供了一种新工具,包括番茄以及可能在其他植物中的分子和物理图谱绘制、突变分析和克隆策略。