Serrano Raquel, Ruiz Amparo, Bernal Dolores, Chambers James R, Ariño Joaquín
Departament de Bioquímica i Biologia Molecular, Facultat de Veterinària, Universitat Autònoma de Barcelona, Bellaterra, E-08193, Barcelona, Spain.
Mol Microbiol. 2002 Dec;46(5):1319-33. doi: 10.1046/j.1365-2958.2002.03246.x.
The short-time transcriptional response of yeast cells to a mild increase in external pH (7.6) has been investigated using DNA microarrays. A total of 150 genes increased their mRNA level at least twofold within 45 min. Alkalinization resulted in the repression of 232 genes. The response of four upregulated genes, ENA1 (encoding a Na+-ATPase also induced by saline stress) and PHO84, PHO89 and PHO12 (encoding genes upregulated by phosphate starvation), was characterized further. The alkaline response of ENA1 was not affected by mutation of relevant genes involved in osmotic or oxidative signalling, but was decreased in calcineurin and rim101 mutants. Mapping of the ENA1 promoter revealed two pH-responsive regions. The response of the upstream region was fully abolished by the drug FK506 or mutation of CRZ1 (a transcription factor activated by calcium/calcineurin), whereas the response of the downstream region was essentially calcium independent. PHO84 and PHO12 responses were unaffected in crz1 cells, but required the presence of Pho2 and Pho4. In contrast, part of the alkali-induced expression of PHO89 was maintained in pho4 or pho2 cells, but was fully abolished in a crz1 strain or in the presence of FK506. Heterologous promoters carrying the minimal calcineurin-dependent response elements found in ENA1 or FKS2 were able to drive alkaline pH-induced expression. These results demonstrate that the transcriptional response to alkaline pH involves different signalling mechanisms, and that calcium signalling is a relevant component of this response.
利用DNA微阵列研究了酵母细胞对外界pH值轻度升高(7.6)的短期转录反应。共有150个基因在45分钟内其mRNA水平至少增加了两倍。碱化导致232个基因的表达受到抑制。对四个上调基因ENA1(编码一种也受盐胁迫诱导的Na + -ATP酶)以及PHO84、PHO89和PHO12(编码受磷酸盐饥饿上调的基因)的反应进行了进一步表征。ENA1的碱性反应不受参与渗透或氧化信号传导的相关基因突变的影响,但在钙调神经磷酸酶和rim101突变体中有所降低。ENA1启动子的定位揭示了两个pH反应区域。上游区域的反应被药物FK506或CRZ1(一种由钙/钙调神经磷酸酶激活的转录因子)的突变完全消除,而下游区域的反应基本上与钙无关。PHO84和PHO12的反应在crz1细胞中不受影响,但需要Pho2和Pho4的存在。相反,PHO89的部分碱诱导表达在pho4或pho2细胞中得以维持,但在crz1菌株中或存在FK506时被完全消除。携带ENA1或FKS2中发现的最小钙调神经磷酸酶依赖性反应元件的异源启动子能够驱动碱性pH诱导的表达。这些结果表明,对碱性pH的转录反应涉及不同的信号传导机制,并且钙信号是该反应的一个相关组成部分。