Gregerson R, McLean M, Beld M, Gerats A G, Strommer J
Department of Genetics, University of Georgia, Athens 30602.
Plant Mol Biol. 1991 Jul;17(1):37-48. doi: 10.1007/BF00036804.
A genomic clone for an alcohol dehydrogenase (Adh) gene has been isolated from Petunia hybrida cv. V30 by screening a Petunia genomic library with a maize Adh1 probe. A combination of RFLP and allozyme segregation data failed to demonstrate which of two Adh loci, both of which map to chromosome 4, was the source of the cloned gene. The product of the cloned genes has been identified unequivocally by a transient expression assay in Petunia protoplasts. We have designated this gene Petunia Adh1. The expression of this gene is tightly regulated in the developing anther, where its gene product is the predominant ADH isozyme. It is anaerobically inducible in roots, stems and leaves of seedlings. The induction of enzyme activity is correlated with induction of Adh1 mRNA.
通过用玉米Adh1探针筛选矮牵牛基因组文库,从矮牵牛杂交种cv. V30中分离出一个酒精脱氢酶(Adh)基因的基因组克隆。限制性片段长度多态性(RFLP)和等位酶分离数据的组合未能证明两个均定位于4号染色体的Adh基因座中哪一个是克隆基因的来源。通过在矮牵牛原生质体中的瞬时表达试验,已明确鉴定出克隆基因的产物。我们将该基因命名为矮牵牛Adh1。该基因的表达在发育中的花药中受到严格调控,其基因产物是主要的ADH同工酶。它在幼苗的根、茎和叶中可被厌氧诱导。酶活性的诱导与Adh1 mRNA的诱导相关。