Jones Mark A, Raymond Marjorie J, Smirnoff Nicholas
School of Biosciences, University of Exeter, Geoffrey Pope Building, Stocker Road, UK.
Plant J. 2006 Jan;45(1):83-100. doi: 10.1111/j.1365-313X.2005.02609.x.
Root-hair morphogenesis is a model for studying the genetic regulation of plant cell development, and double-mutant analyses have revealed a complex genetic network underlying the development of this type of cell. Therefore, to increase knowledge of gene expression in root hairs and to identify new genes involved in root-hair morphogenesis, the transcriptomes of the root-hair differentiation zone of wild-type (WT) plants and a tip-growth defective root-hair mutant, rhd2-1, were compared using Affymetrix ATH1 GeneChips. A set of 606 genes with significantly greater expression in WT plants defines the 'root-hair morphogenesis transcriptome'. Compared with the whole genome, this set is highly enriched in genes known to be involved in root-hair morphogenesis. The additional gene families and functional groups enriched in the root-hair morphogenesis transcriptome are cell wall enzymes, hydroxyproline-rich glycoproteins (extensins) and arabinogalactan proteins, peroxidases, receptor-like kinases and proteins with predicted glycosylphosphatidylinositol (GPI) anchors. To discover new root-hair genes, 159 T-DNA insertion lines identified from the root-hair morphogenesis transcriptome were screened for defects in root-hair morphogenesis. This identified knockout mutations in six genes (RHM1-RHM6) that affected root-hair morphogenesis and that had not previously been identified at the molecular level: At2g03720 (similar to Escherichia coli universal stress protein); At3g54870 (armadillo-repeat containing kinesin-related protein); At4g18640 (leucine-rich repeat receptor-like kinase subfamily VI); At4g26690 (glycerophosphoryl diester phosphodiesterase-like GPI-anchored protein); At5g49270 (COBL9 GPI-anchored protein) and At5g65090 (inositol-1,4,5 triphosphate 5-phosphatase-like protein). The mutants were transcript null, their root-hair phenotypes were characterized and complementation testing with uncloned root-hair genes was performed. The results suggest a role for GPI-anchored proteins and lipid rafts in root-hair tip growth because two of these genes (At4g26690 and At5g49270) encode predicted GPI-anchored proteins likely to be associated with lipid rafts, and several other genes previously shown to be required for root-hair development also encode proteins associated with sterol-rich lipid rafts.
根毛形态发生是研究植物细胞发育遗传调控的一个模型,双突变分析揭示了这种细胞发育背后的复杂遗传网络。因此,为了增加对根毛中基因表达的了解并鉴定参与根毛形态发生的新基因,使用Affymetrix ATH1基因芯片比较了野生型(WT)植物和一个顶端生长缺陷型根毛突变体rhd2-1的根毛分化区转录组。一组在WT植物中表达显著更高的606个基因定义了“根毛形态发生转录组”。与整个基因组相比,这一组在已知参与根毛形态发生的基因中高度富集。根毛形态发生转录组中额外富集的基因家族和功能组包括细胞壁酶、富含羟脯氨酸的糖蛋白(伸展蛋白)和阿拉伯半乳聚糖蛋白、过氧化物酶、类受体激酶以及具有预测糖基磷脂酰肌醇(GPI)锚定的蛋白质。为了发现新的根毛基因,对从根毛形态发生转录组中鉴定出的159个T-DNA插入系进行了根毛形态发生缺陷筛选。这确定了六个影响根毛形态发生且以前在分子水平未被鉴定的基因(RHM1-RHM6)中的敲除突变:At2g03720(类似于大肠杆菌通用应激蛋白);At3g54870(含有犰狳重复序列的驱动蛋白相关蛋白);At4g18640(富含亮氨酸重复序列的类受体激酶亚家族VI);At4g26690(甘油磷酸二酯磷酸二酯酶样GPI锚定蛋白);At5g49270(COBL9 GPI锚定蛋白)和At5g65090(肌醇-1,4,5-三磷酸5-磷酸酶样蛋白)。对这些突变体进行了转录本缺失分析,对其根毛表型进行了表征,并使用未克隆的根毛基因进行了互补测试。结果表明GPI锚定蛋白和脂筏在根毛顶端生长中起作用,因为其中两个基因(At4g26690和At5g49270)编码可能与脂筏相关的预测GPI锚定蛋白,并且先前显示对根毛发育必需的其他几个基因也编码与富含固醇的脂筏相关的蛋白质。