Xiao Huogen, Siddiqua Mahbuba, Braybrook Siobhan, Nassuth Annette
Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario N1G 2W1, Canada.
Plant Cell Environ. 2006 Jul;29(7):1410-21. doi: 10.1111/j.1365-3040.2006.01524.x.
The C-repeat (CRT)-binding factor/dehydration-responsive element (DRE) binding protein 1 (CBF/ DREB1) transcription factors control an important pathway for increased freezing and drought tolerance in plants. Three CBF/DREB1-like genes, CBF 1-3, were isolated from both freezing-tolerant wild grape (Vitis riparia) and freezing-sensitive cultivated grape (Vitis vinifera). The deduced proteins in V. riparia are 63-70% identical to each other and 96-98% identical to the corresponding proteins in V. vinifera. All Vitis CBF proteins are 42-51% identical to AtCBF1 and contain CBF-specific amino acid motifs, supporting their identification as CBF proteins. Grape CBF sequences are unique in that they contain 20-29 additional amino acids and three serine stretches. Agro-infiltration experiments revealed that VrCBF1b localizes to the nucleus. VrCBF1a, VrCBF1b and VvCBF1 activated a green fluorescent protein (GFP) or glucuronidase (GUS) reporter gene behind CRT-containing promoters. Expression of the endogenous CBF genes was low at ambient temperature and enhanced upon low temperature (4 degrees C) treatment, first for CBF1, followed by CBF2, and about 2 d later by CBF3. No obvious significant difference was observed between V. riparia and V. vinifera genes. The expression levels of all three CBF genes were higher in young tissues than in older tissues. CBF1, 2 and 3 transcripts also accumulated in response to drought and exogenous abscisic acid (ABA) treatment, indicating that grape contains unique CBF genes.
C-重复序列(CRT)结合因子/脱水响应元件(DRE)结合蛋白1(CBF/DREB1)转录因子控制着植物增强抗冻性和耐旱性的一条重要途径。从耐冻野生葡萄(河岸葡萄)和冻敏感栽培葡萄(酿酒葡萄)中分离出了3个类CBF/DREB1基因,即CBF 1 - 3。河岸葡萄中推导的蛋白质彼此间有63 - 70%的同一性,与酿酒葡萄中的相应蛋白质有96 - 98%的同一性。所有葡萄CBF蛋白与拟南芥CBF1有42 - 51%的同一性,并含有CBF特异性氨基酸基序,这支持将它们鉴定为CBF蛋白。葡萄CBF序列的独特之处在于它们含有另外20 - 29个氨基酸和三个丝氨酸延伸段。农杆菌浸润实验表明,河岸葡萄CBF1b定位于细胞核。河岸葡萄CBF1a、河岸葡萄CBF1b和酿酒葡萄CBF1激活了含CRT启动子下游的绿色荧光蛋白(GFP)或葡糖醛酸酶(GUS)报告基因。内源CBF基因在环境温度下表达较低,低温(4℃)处理后表达增强,首先是CBF1,接着是CBF2,约2天后是CBF3。河岸葡萄和酿酒葡萄基因之间未观察到明显的显著差异。所有三个CBF基因在幼嫩组织中的表达水平都高于老组织。CBF1、2和3转录本也在干旱和外源脱落酸(ABA)处理时积累,表明葡萄含有独特的CBF基因。