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A single-repeat R3-MYB transcription factor MYBC1 negatively regulates freezing tolerance in Arabidopsis.

机译:单重复R3-MYB转录因子MYBC1负调节拟南芥的冷冻耐受性。

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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.
机译:我们之前已经将编码单重复R3-MYB蛋白的MYBC1基因确定为假定的渗透反应基因。但是,尚无R3-MYB转录因子调节渗透压耐受性的报道。因此,我们试图阐明MYBC1应对渗透胁迫的功能。实时RT-PCR分析表明,MYBC1表达在转录水平上响应于寒冷,脱水,盐度和外源ABA。 mybc1突变体表现出更高的抗冰冻耐受性,而35S :: MYBC1转基因植物表现出降低的抗寒性。但是,与冷胁迫相比,mybc1突变体或35S :: MYBC1转基因植物中的一些冷应答基因,包括CBF / DREB基因,KIN1,ADC1,ADC2和ZAT12的转录水平没有改变。野生型。调查了公开可用的微阵列分析结果,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能够负性调节CBF独立途径中拟南芥的抗冻性。在携带MYBC1启动子驱动的β-葡萄糖醛酸苷酶(GUS)构建体的转基因拟南芥中,在所有组织中均观察到了GUS活性,并且在血管组织中相对较强。融合的MYBC1和GFP蛋白显示MYBC1仅位于核区室中。

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