Dumas R, Curien G, DeRose R T, Douce R
Unité Mixte CNRS/Rhône-Poulenc (Unité associée au Centre National de la Recherche Scientifique, U. M. 41), Lyon, France.
Biochem J. 1993 Sep 15;294 ( Pt 3)(Pt 3):821-8. doi: 10.1042/bj2940821.
Towards the goal of gaining a better understanding of the molecular mechanisms controlling branched-chain-amino-acid biosynthesis in plants, we have isolated, sequenced and characterized a gene encoding acetohydroxy acid isomero-reductase (ketol-acid reductoisomerase) from Arabidopsis thaliana (thale cress). Comparison between the acetohydroxy acid isomeroreductase cDNA and the genomic sequence has allowed us to determine the exon structure of the coding region. The isolated acetohydroxy acid isomeroreductase gene is distributed over approx. 4.5 kbp and contains nine introns (79-347 bp). The transcriptional start site was found to be 52 bp upstream of the translational initiation site. Southern-blot analysis of A. thaliana genomic DNA shows that the acetohydroxy acid isomeroreductase is encoded by a single-copy gene.
为了更好地理解植物中控制支链氨基酸生物合成的分子机制,我们从拟南芥(鼠耳芥)中分离、测序并鉴定了一个编码乙酰羟酸异构还原酶(酮醇酸还原异构酶)的基因。通过比较乙酰羟酸异构还原酶的cDNA和基因组序列,我们得以确定编码区的外显子结构。分离出的乙酰羟酸异构还原酶基因分布在约4.5千碱基对(kbp)上,包含9个内含子(79 - 347碱基对)。转录起始位点位于翻译起始位点上游52碱基对处。对拟南芥基因组DNA的Southern杂交分析表明,乙酰羟酸异构还原酶由单拷贝基因编码。