Institute of Genetics, University of Amsterdam, Kruislaan 318, NL-1098, SM Amsterdam, The Netherlands.
Theor Appl Genet. 1984 May;68(1-2):29-34. doi: 10.1007/BF00252307.
In root and flower corolla tissue of Petunia several anodic moving peroxidase isoenzymes are present, which cannot be detected in other organs. Alleles of the gene prxF control the presence or absence of several peroxidases that are only present in flower corolla tissue. Alleles of the gene prxG code for two peroxidases that can only be detected in root tissue. In addition to mutations of prxG that cause a change in the electrophoretic mobility of the PRXg enzymes, a mutation was also found that causes the absence of expression in enzyme activity. Crossing experiments indicated that this mutation is located in the gene prxG. Peroxidases encoded by the gene prxH were only found in root tissue. Two alleles of prxH were identified by electrophoretic variation; one allele is responsible for a single band, whereas the other allele could be recognized by a double-banded phenotype. The double-banded PRXh phenotype is suggested to be caused by tandem duplication, followed by mutation in one of the genes. A third prxH allele could be identified by the absence of PRXh activity. The genes prxF, prxG, and prxH were shown to be located on chromosome VII, with the following gene order: prxG-An4-lapB-gpiB-prxH-prxF.
矮牵牛的根和花被组织中存在几种阳极移动过氧化物酶同工酶,在其他器官中检测不到。prxF 基因的等位基因控制仅存在于花被组织中的几种过氧化物酶的存在或缺失。prxG 基因编码的两种过氧化物酶只能在根组织中检测到。除了导致 PRXg 酶电泳迁移率发生变化的 prxG 突变外,还发现了一种导致酶活性缺失的表达缺失突变。杂交实验表明,该突变位于 prxG 基因中。由 prxH 基因编码的过氧化物酶仅在根组织中发现。通过电泳变化鉴定了 prxH 的两个等位基因;一个等位基因负责形成单一条带,而另一个等位基因可以通过双带表型识别。双带 PRXh 表型被认为是串联重复,然后在其中一个基因中发生突变引起的。可以通过 PRXh 活性缺失来鉴定第三个 prxH 等位基因。prxF、prxG 和 prxH 基因被证明位于染色体 VII 上,基因顺序如下:prxG-An4-lapB-gpiB-prxH-prxF。