Millar Anthony A, Gubler Frank
Commonwealth Scientific and Industrial Research Organization, Division of Plant Industry, Canberra ACT 2601, Australia.
Plant Cell. 2005 Mar;17(3):705-21. doi: 10.1105/tpc.104.027920. Epub 2005 Feb 18.
The functions of the vast majority of genes encoding R2R3 MYB domain proteins remain unknown. The closely related MYB33 and MYB65 genes of Arabidopsis thaliana have high sequence similarity to the barley (Hordeum vulgare) GAMYB gene. T-DNA insertional mutants were isolated for both genes, and a myb33 myb65 double mutant was defective in anther development. In myb33 myb65 anthers, the tapetum undergoes hypertrophy at the pollen mother cell stage, resulting in premeiotic abortion of pollen development. However, myb33 myb65 sterility was conditional, where fertility increased both under higher light or lower temperature conditions. Thus, MYB33/MYB65 facilitate, but are not essential for, anther development. Neither single mutant displayed a phenotype, implying that MYB33 and MYB65 are functionally redundant. Consistent with functional redundancy, promoter-beta-glucuronidase (GUS) fusions of MYB33 and MYB65 gave identical expression patterns in flowers (sepals, style, receptacle, anther filaments, and connective but not in anthers themselves), shoot apices, and root tips. By contrast, expression of a MYB33:GUS translational fusion in flowers was solely in young anthers (consistent with the male sterile phenotype), and no staining was seen in shoot meristems or root tips. A microRNA target sequence is present in the MYB genes, and mutating this sequence in the MYB33:GUS fusion results in an expanded expression pattern, in tissues similar to that observed in the promoter-GUS lines, implying that the microRNA target sequence is restricting MYB33 expression. Arabidopsis transformed with MYB33 containing the mutated microRNA target had dramatic pleiotrophic developmental defects, suggesting that restricting MYB33 expression, especially in the shoot apices, is essential for proper plant development.
绝大多数编码R2R3 MYB结构域蛋白的基因功能仍不清楚。拟南芥中密切相关的MYB33和MYB65基因与大麦(Hordeum vulgare)GAMYB基因具有高度的序列相似性。分离出了这两个基因的T-DNA插入突变体,myb33 myb65双突变体在花药发育方面存在缺陷。在myb33 myb65花药中,绒毡层在花粉母细胞阶段发生肥大,导致花粉发育在减数分裂前流产。然而,myb33 myb65的不育是有条件的,在较高光照或较低温度条件下育性会增加。因此,MYB33/MYB65促进花药发育,但并非花药发育所必需。单个突变体均未表现出表型,这意味着MYB33和MYB65在功能上是冗余的。与功能冗余一致,MYB33和MYB65的启动子-β-葡萄糖醛酸酶(GUS)融合在花(萼片、花柱、花托、花药花丝和药隔,但花药本身除外)、茎尖和根尖中呈现相同的表达模式。相比之下,MYB33:GUS翻译融合在花中的表达仅在幼嫩花药中(与雄性不育表型一致),在茎尖分生组织或根尖中未见染色。MYB基因中存在一个微小RNA靶序列,在MYB33:GUS融合中突变该序列会导致表达模式扩展,在与启动子-GUS系中观察到的组织相似的组织中表达,这意味着微小RNA靶序列限制了MYB33的表达。用含有突变微小RNA靶标的MYB33转化拟南芥会出现严重的多效性发育缺陷,这表明限制MYB33的表达,尤其是在茎尖中的表达,对于植物的正常发育至关重要。