Xu X, Dietrich C R, Delledonne M, Xia Y, Wen T J, Robertson D S, Nikolau B J, Schnable P S
Department of Zoology, Iowa State University, Ames 50011, USA.
Plant Physiol. 1997 Oct;115(2):501-10. doi: 10.1104/pp.115.2.501.
The gl8 locus of maize (Zea mays L.) was previously defined by a mutation that reduces the amount and alters the composition of seedling cuticular waxes. Sixty independently derived gl8 mutant alleles were isolated from stocks that carried the Mutator transposon system. A DNA fragment that contains a Mu8 transposon and that co-segregates with one of these alleles, gl8-Mu3142, was identified and cloned. DNA flanking the Mu8 transposon was shown via allelic cross-referencing experiments to represent the gl8 locus. The gl8 probe revealed a 1.4-kb transcript present in wild-type seedling leaves and, in lesser amounts, in other organs and at other developmental stages. The amino acid sequence deduced from an apparently full-length gl8 cDNA exhibits highly significant sequence similarity to a group of enzymes from plants, eubacteria, and mammals that catalyzes the reduction of ketones. This finding suggests that the GL8 protein probably functions as a reductase during fatty acid elongation in the cuticular wax biosynthetic pathway.
玉米(Zea mays L.)的gl8位点先前是由一个突变定义的,该突变会减少幼苗表皮蜡质的数量并改变其组成。从携带Mutator转座子系统的材料中分离出60个独立衍生的gl8突变等位基因。鉴定并克隆了一个包含Mu8转座子且与其中一个等位基因gl8-Mu3142共分离的DNA片段。通过等位基因交叉参照实验表明,Mu8转座子侧翼的DNA代表gl8位点。gl8探针显示在野生型幼苗叶片中存在一个1.4 kb的转录本,在其他器官和其他发育阶段含量较少。从一个明显全长的gl8 cDNA推导的氨基酸序列与来自植物、真细菌和哺乳动物的一组催化酮还原的酶具有高度显著的序列相似性。这一发现表明,GL8蛋白可能在表皮蜡质生物合成途径的脂肪酸延长过程中作为一种还原酶发挥作用。