Baum J A, Geever R, Giles N H
Mol Cell Biol. 1987 Mar;7(3):1256-66. doi: 10.1128/mcb.7.3.1256-1266.1987.
The qa-1F regulatory gene of Neurospora crassa encodes an activator protein required for quinic acid induction of transcription in the qa gene cluster. This activator protein was expressed in insect cell culture with a baculovirus expression vector. The activator binds to 13 sites in the gene cluster that are characterized by a conserved 16-base-pair sequence of partial dyad symmetry. One site is located between the divergently transcribed qa-1F and qa-1S regulatory genes, corroborating prior evidence that qa-1F is autoregulated and controls expression of the qa-1S repressor. Multiple upstream sites located at variable positions 5' to the qa structural genes appear to allow for greater transcriptional control by qa-1F. Full-length and truncated activator peptides were synthesized in vitro, and the DNA-binding domain was localized to the first 183 amino acids. A 28-amino acid sequence within this region shows striking homology to N-terminal sequences from other lower-eucaryotic activator proteins. A qa-1F(Ts) mutation is located within this putative DNA-binding domain.
粗糙脉孢菌的qa-1F调控基因编码一种激活蛋白,该蛋白是奎尼酸诱导qa基因簇转录所必需的。这种激活蛋白在昆虫细胞培养物中通过杆状病毒表达载体进行表达。该激活蛋白与基因簇中的13个位点结合,这些位点的特征是具有部分二元对称的保守16碱基对序列。其中一个位点位于反向转录的qa-1F和qa-1S调控基因之间,证实了之前关于qa-1F是自我调控并控制qa-1S阻遏物表达的证据。位于qa结构基因5'端可变位置的多个上游位点似乎允许qa-1F进行更大程度的转录控制。全长和截短的激活肽在体外合成,并且DNA结合结构域定位于前183个氨基酸。该区域内的一个28个氨基酸的序列与其他低等真核生物激活蛋白的N端序列具有显著的同源性。一个qa-1F(Ts)突变位于这个假定的DNA结合结构域内。