Napoli CA, Fahy D, Wang HY, Taylor LP
Department of Plant Sciences, University of Arizona, Tucson, Arizona 85721 (C.A.N., H.-Y.W.).
Plant Physiol. 1999 Jun;120(2):615-22. doi: 10.1104/pp.120.2.615.
A mutation in an inbred line of petunia (Petunia hybrida) produces a reduction in the deep-purple corolla pigmentation and changes the anther color from yellow to white. In addition, the mutant, designated white anther (wha), is functionally male sterile. The inability of pollen from wha plants to germinate in vitro provides a physiological basis for the lack of seed set observed in self-crosses of the mutant. Biochemical complementation with nanomolar amounts of kaempferol, a flavonol aglycone, confirms that the inability of the wha pollen to germinate is due to a lack of this essential compound. Transgenic complementation with a functional ChsA (Chalcone synthase A) cDNA suggests that the genetic lesion responsible for the wha phenotype is in Chs, the gene for the first enzyme in the flavonol biosynthesis pathway. The genetic background of the parental line, as well as the pollen phenotype, allowed us to deduce that the wha mutation is in ChsA. To our knowledge, wha is the first induced, nontransgenic Chs mutant described in petunia, and analysis of the mutation confirms earlier molecular and genetic observations that only two Chs genes (A and J) are expressed in reproductive tissues and that they are differentially regulated in corolla and anther.
矮牵牛(Petunia hybrida)自交系中的一个突变导致深紫色花冠色素沉着减少,并使花药颜色从黄色变为白色。此外,该突变体被命名为白花药(wha),在功能上是雄性不育的。wha植株的花粉在体外无法萌发,这为该突变体自交时观察到的不结籽现象提供了生理基础。用纳摩尔量的山奈酚(一种黄酮醇苷元)进行生化互补实验,证实了wha花粉无法萌发是由于缺乏这种必需化合物。用功能性查尔酮合酶A(Chalcone synthase A,ChsA)cDNA进行转基因互补实验表明,导致wha表型的基因损伤位于Chs,即黄酮醇生物合成途径中第一种酶的基因。亲本系的遗传背景以及花粉表型使我们推断wha突变位于ChsA。据我们所知,wha是矮牵牛中描述的第一个诱导型、非转基因Chs突变体,对该突变的分析证实了早期的分子和遗传学观察结果,即在生殖组织中只有两个Chs基因(A和J)表达,并且它们在花冠和花药中受到不同的调控。