Plant Bioengineering Laboratory, Northeast Agricultural University, Harbin 150030, PR China.
Biochem Biophys Res Commun. 2010 Apr 16;394(4):1018-23. doi: 10.1016/j.bbrc.2010.03.114. Epub 2010 Mar 21.
We had previously identified the MYBC1 gene, which encodes a single-repeat R3-MYB protein, as a putative osmotic responding gene; however, no R3-MYB transcription factor has been reported to regulate osmotic stress tolerance. Thus, we sought to elucidate the function of MYBC1 in response to osmotic stresses. Real-time RT-PCR analysis indicated that MYBC1 expression responded to cold, dehydration, salinity and exogenous ABA at the transcript level. mybc1 mutants exhibited an increased tolerance to freezing stress, whereas 35S::MYBC1 transgenic plants exhibited decreased cold tolerance. Transcript levels of some cold-responsive genes, including CBF/DREB genes, KIN1, ADC1, ADC2 and ZAT12, though, were not altered in the mybc1 mutants or the 35S::MYBC1 transgenic plants in response to cold stress, as compared to the wild type. Microarray analysis results that are publically available were investigated and found transcript level of MYBC1 was not altered by overexpression of CBF1, CBF2, and CBF3, suggesting that MYBC1 is not down regulated by these CBF family members. Together, these results suggested that MYBC1is capable of negatively regulating the freezing tolerance of Arabidopsis in the CBF-independent pathway. In transgenic Arabidopsis carrying an MYBC1 promoter driven beta-glucuronidase (GUS) construct, GUS activity was observed in all tissues and was relatively stronger in the vascular tissues. Fused MYBC1 and GFP protein revealed that MYBC1 was localized exclusively in the nuclear compartment.
我们先前鉴定了 MYBC1 基因,它编码一个单重复 R3-MYB 蛋白,是一个假定的渗透响应基因;然而,没有报道 R3-MYB 转录因子调节渗透胁迫耐受性。因此,我们试图阐明 MYBC1 在应对渗透胁迫中的功能。实时 RT-PCR 分析表明,MYBC1 表达在转录水平上响应冷、脱水、盐度和外源 ABA。mybc1 突变体对冷冻胁迫表现出更高的耐受性,而 35S::MYBC1 转基因植物对寒冷的耐受性降低。一些冷响应基因,包括 CBF/DREB 基因、KIN1、ADC1、ADC2 和 ZAT12 的转录水平,在 mybc1 突变体或 35S::MYBC1 转基因植物中并未因冷胁迫而改变,与野生型相比。我们研究了可公开获得的微阵列分析结果,发现 MYBC1 的转录水平没有因 CBF1、CBF2 和 CBF3 的过表达而改变,这表明 MYBC1 不受这些 CBF 家族成员的下调。总之,这些结果表明,MYBC1 能够在 CBF 非依赖途径中负调控拟南芥的抗冻性。在携带 MYBC1 启动子驱动的β-葡萄糖醛酸酶(GUS)构建体的转基因拟南芥中,在所有组织中都观察到 GUS 活性,在血管组织中相对较强。融合的 MYBC1 和 GFP 蛋白表明,MYBC1 仅定位于核区室。