Snowden Kimberley C, Simkin Andrew J, Janssen Bart J, Templeton Kerry R, Loucas Holly M, Simons Joanne L, Karunairetnam Sakuntala, Gleave Andrew P, Clark David G, Klee Harry J
HortResearch, Private Bag 92169, Mt. Albert, Auckland, New Zealand.
Plant Cell. 2005 Mar;17(3):746-59. doi: 10.1105/tpc.104.027714. Epub 2005 Feb 10.
Carotenoids and carotenoid cleavage products play an important and integral role in plant development. The Decreased apical dominance1 (Dad1)/PhCCD8 gene of petunia (Petunia hybrida) encodes a hypothetical carotenoid cleavage dioxygenase (CCD) and ortholog of the MORE AXILLARY GROWTH4 (MAX4)/AtCCD8 gene. The dad1-1 mutant allele was inactivated by insertion of an unusual transposon (Dad-one transposon), and the dad1-3 allele is a revertant allele of dad1-1. Consistent with its role in producing a graft-transmissible compound that can alter branching, the Dad1/PhCCD8 gene is expressed in root and shoot tissue. This expression is upregulated in the stems of the dad1-1, dad2, and dad3 increased branching mutants, indicating feedback regulation of the gene in this tissue. However, this feedback regulation does not affect the root expression of Dad1/PhCCD8. Overexpression of Dad1/PhCCD8 in the dad1-1 mutant complemented the mutant phenotype, and RNA interference in the wild type resulted in an increased branching phenotype. Other differences in phenotype associated with the loss of Dad1/PhCCD8 function included altered timing of axillary meristem development, delayed leaf senescence, smaller flowers, reduced internode length, and reduced root growth. These data indicate that the substrate(s) and/or product(s) of the Dad1/PhCCD8 enzyme are mobile signal molecules with diverse roles in plant development.
类胡萝卜素及其裂解产物在植物发育过程中发挥着重要且不可或缺的作用。矮牵牛(Petunia hybrida)的顶端优势降低1(Dad1)/PhCCD8基因编码一种假定的类胡萝卜素裂解双加氧酶(CCD),是多腋芽生长4(MAX4)/拟南芥CCD8基因的直系同源基因。dad1 - 1突变等位基因因插入一个异常转座子(Dad - one转座子)而失活,dad1 - 3等位基因是dad1 - 1的回复等位基因。与其在产生可改变分枝的嫁接可传递化合物中的作用一致,Dad1/PhCCD8基因在根和地上组织中表达。这种表达在dad1 - 1、dad2和dad3分枝增加突变体的茎中上调,表明该基因在该组织中存在反馈调节。然而,这种反馈调节并不影响Dad1/PhCCD8在根中的表达。在dad1 - 1突变体中过表达Dad1/PhCCD8可互补突变表型,而在野生型中进行RNA干扰则导致分枝表型增加。与Dad1/PhCCD8功能丧失相关的其他表型差异包括腋生分生组织发育时间改变、叶片衰老延迟、花朵变小、节间长度缩短以及根生长减少。这些数据表明,Dad1/PhCCD8酶的底物和/或产物是在植物发育中具有多种作用的移动信号分子。