Gugneja S, Virbasius C M, Scarpulla R C
Department of Cell and Molecular Biology, Northwestern University Medical School, Chicago, Illinois 60611, USA.
Mol Cell Biol. 1996 Oct;16(10):5708-16. doi: 10.1128/MCB.16.10.5708.
Nuclear respiratory factors 1 and 2 (NRF-1 and NRF-2) are ubiquitous transcription factors that have been implicated in the control of nuclear genes required for respiration, heme biosynthesis, and mitochondrial DNA transcription and replication. Recently, both factors have been found to be major transcriptional determinants for a subset of these genes that define a class of simple promoters involved in respiratory chain expression. Here, functional domains required for transactivation by NRF-1 have been defined. An atypical nuclear localization signal resides in a conserved amino-terminal region adjacent to the DNA binding domain and consists of functionally redundant clusters of basic residues. A second domain in the carboxy-terminal half of the molecule is necessary for transcriptional activation. The activation domains of both NRF-1 and NRF-2 were extensively characterized by both deletion and alanine substitution mutagenesis. The results show that these domains do not fall into known classes defined by a preponderance of amino acid residues, including glutamines, prolines, or isoleucines, as found in other eukaryotic activators. Rather, in both factors, a series of tandemly arranged clusters of hydrophobic amino acids were required for activation. Although all of the functional clusters contain glutamines, the glutamines differ from the hydrophobic residues in that they are inconsequential for activation. Unlike the NRF-2 domain, which contains its essential hydrophobic motifs within 40 residues, the NRF-1 domain spans about 40% of the molecule and appears to have a bipartite structure. The findings indicate that NRF-1 and NRF-2 utilize similar hydrophobic structural motifs for activating transcription.
核呼吸因子1和2(NRF - 1和NRF - 2)是普遍存在的转录因子,与呼吸、血红素生物合成以及线粒体DNA转录和复制所需的核基因调控有关。最近,人们发现这两种因子是这些基因子集中的主要转录决定因素,这些基因定义了一类参与呼吸链表达的简单启动子。在此,已确定了NRF - 1反式激活所需的功能结构域。一个非典型的核定位信号位于与DNA结合结构域相邻的保守氨基末端区域,由功能冗余的碱性残基簇组成。分子羧基末端一半的第二个结构域对于转录激活是必需的。通过缺失和丙氨酸取代诱变对NRF - 1和NRF - 2的激活结构域进行了广泛表征。结果表明,这些结构域不属于由其他真核激活因子中大量存在的氨基酸残基(包括谷氨酰胺、脯氨酸或异亮氨酸)所定义的已知类别。相反,在这两种因子中,激活需要一系列串联排列的疏水氨基酸簇。虽然所有功能簇都含有谷氨酰胺,但谷氨酰胺与疏水残基不同,因为它们对激活无关紧要。与NRF - 2结构域不同,NRF - 2结构域在40个残基内包含其必需的疏水基序,而NRF - 1结构域跨越分子的约40%,似乎具有二分结构。这些发现表明,NRF - 1和NRF - 2利用相似的疏水结构基序来激活转录。