Hajós-Novák M, Nagy A H, Dallmann G
Department of Genetics and Plant Breeding, Gödöllö Agriculture University, Hungary.
Acta Biol Hung. 1997;48(1):87-94.
The results of two separate experiment are presented in this paper. In the first experiment pollen assays were carried out in Wf9 tetraploid maize plants in order to decide whether the lack of the ADH enzyme activity in the pollen grains was caused by a 'O' allele or an active transposon. On the basis of the results we suppose that the reduced ADH enzyme activity in the pollen grains is the result of a transposon affecting only the gametophyte. In the second experiment a maize Adh1-S genomic clone was constructed by polymerase chain reaction (PCR) and used as a probe to detect polymoprhism around the Adh1 gene in W117 S18 tetraploid maize sublines. The PCR20-EcoRI clone-enzyme combination resulted in a monomorphic RFLP pattern. The PCR20-Bgl II probe-enzyme combination yielded a multiple-banded pattern.
本文展示了两个独立实验的结果。在第一个实验中,对Wf9四倍体玉米植株进行了花粉检测,以确定花粉粒中ADH酶活性的缺乏是由“O”等位基因还是活跃的转座子引起的。根据实验结果,我们推测花粉粒中ADH酶活性降低是仅影响配子体的转座子的结果。在第二个实验中,通过聚合酶链反应(PCR)构建了玉米Adh1-S基因组克隆,并将其用作探针来检测W117 S18四倍体玉米亚系中Adh1基因周围的多态性。PCR20-EcoRI克隆-酶组合产生了单态性的RFLP模式。PCR20-Bgl II探针-酶组合产生了多条带的模式。