Fernandes L, Rodrigues-Pousada C, Struhl K
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Mol Cell Biol. 1997 Dec;17(12):6982-93. doi: 10.1128/MCB.17.12.6982.
Saccharomyces cerevisiae contains eight members of a novel and fungus-specific family of bZIP proteins that is defined by four atypical residues on the DNA-binding surface. Two of these proteins, Yap1 and Yap2, are transcriptional activators involved in pleiotropic drug resistance. Although initially described as AP-1 factors, at least four Yap proteins bind most efficiently to TTACTAA, a sequence that differs at position +/-2 from the optimal AP-1 site (TGACTCA); further, a Yap-like derivative of the AP-1 factor Gcn4 (A239Q S242F) binds efficiently to the Yap recognition sequence. Molecular modeling suggests that the Yap-specific residues make novel contacts and cause physical constraints at the +/-2 position that may account for the distinct DNA-binding specificities of Yap and AP-1 proteins. To various extents, Yap1, Yap2, Yap3, and Yap5 activate transcription from a promoter containing a Yap recognition site. Yap-dependent transcription is abolished in strains containing high levels of protein kinase A; in contrast, Gcn4 transcriptional activity is stimulated by protein kinase A. Interestingly, Yap1 transcriptional activity is stimulated by hydrogen peroxide, whereas Yap2 activity is stimulated by aminotriazole and cadmium. In addition, unlike other yap mutations tested, yap4 (cin5) mutations affect chromosome stability, and they suppress the cold-sensitive phenotype of yap1 mutant strains. Thus, members of the Yap family carry out overlapping but distinct biological functions.
酿酒酵母含有一个新型的、真菌特有的bZIP蛋白家族的八个成员,该家族由DNA结合表面上的四个非典型残基定义。其中两个蛋白Yap1和Yap2是参与多药耐药性的转录激活因子。尽管最初被描述为AP-1因子,但至少有四个Yap蛋白最有效地结合到TTACTAA序列上,该序列在位置+/-2处与最佳AP-1位点(TGACTCA)不同;此外,AP-1因子Gcn4的一个Yap样衍生物(A239Q S242F)能有效地结合到Yap识别序列上。分子建模表明,Yap特异性残基形成了新的接触,并在+/-2位置造成了物理限制,这可能解释了Yap和AP-1蛋白不同的DNA结合特异性。在不同程度上,Yap1、Yap2、Yap3和Yap5能从含有Yap识别位点的启动子激活转录。在含有高水平蛋白激酶A的菌株中,Yap依赖的转录被消除;相反,蛋白激酶A刺激Gcn4的转录活性。有趣的是,过氧化氢刺激Yap1的转录活性,而氨三唑和镉刺激Yap2的活性。此外,与测试的其他yap突变不同,yap4(cin5)突变影响染色体稳定性,并且它们抑制yap1突变菌株的冷敏感表型。因此,Yap家族成员执行重叠但不同的生物学功能。