Sansó Miriam, Gogol Madelaine, Ayté José, Seidel Chris, Hidalgo Elena
Oxidative Stress and Cell Cycle Group, Departament de Ciències Experimentals i de la Salut, Universitat Pompeu Fabra, C/ Dr. Aiguader 88, E-08003 Barcelona, Spain.
Eukaryot Cell. 2008 May;7(5):826-35. doi: 10.1128/EC.00465-07. Epub 2008 Mar 28.
The mitogen-activated protein kinase Sty1 is essential for the regulation of transcriptional responses that promote cell survival in response to different types of environmental stimuli in Schizosaccharomyces pombe. Upon stress activation, Sty1 reversibly accumulates in the nucleus, where it stimulates gene expression via the Atf1 transcription factor. The Atf1 protein forms a heterodimer with Pcr1, but the specific role of this association is controversial. We have carried out a comparative analysis of strains lacking these proteins individually. We demonstrate that Atf1 and Pcr1 have similar but not identical roles in S. pombe, since cells lacking Pcr1 do not share all the phenotypes reported for Deltaatf1 cells. Northern blot and microarray analyses demonstrate that the responses to specific stresses of cells lacking either Pcr1 or Atf1 do not fully overlap, and even though most Atf1-dependent genes induced by osmotic stress are also Pcr1 dependent, a subset of genes require only the presence of Atf1 for their induction. Whereas binding of Atf1 to most stress-dependent genes requires the presence of Pcr1, we demonstrate here that Atf1 can bind to the Pcr1-independent promoters in a Deltapcr1 strain in vivo. Furthermore, these analyses show that both proteins have a global repressive effect on stress-dependent and stress-independent genes.
有丝分裂原活化蛋白激酶Sty1对于调节转录反应至关重要,该转录反应可促进粟酒裂殖酵母在应对不同类型环境刺激时的细胞存活。在应激激活后,Sty1可逆地在细胞核中积累,在那里它通过Atf1转录因子刺激基因表达。Atf1蛋白与Pcr1形成异二聚体,但这种关联的具体作用存在争议。我们对单独缺失这些蛋白的菌株进行了比较分析。我们证明Atf1和Pcr1在粟酒裂殖酵母中具有相似但不完全相同的作用,因为缺失Pcr1的细胞并不具有所有报道的Δatf1细胞的表型。Northern印迹和微阵列分析表明,缺失Pcr1或Atf1的细胞对特定应激的反应并不完全重叠,并且尽管大多数由渗透应激诱导的Atf1依赖性基因也是Pcr1依赖性的,但一部分基因的诱导仅需要Atf1的存在。虽然Atf1与大多数应激依赖性基因的结合需要Pcr1的存在,但我们在此证明Atf1在体内可结合Δpcr1菌株中不依赖Pcr1的启动子。此外,这些分析表明这两种蛋白对应激依赖性和应激非依赖性基因均具有全局抑制作用。