Laboratory of Molecular Microbiology, School of Biological Sciences, and Institute of Microbiology, Seoul National University, Seoul, South Korea.
BMC Microbiol. 2012 May 30;12:86. doi: 10.1186/1471-2180-12-86.
In the fission yeast Schizosaccharomyces pombe, the phx1+ (pombe homeobox) gene was initially isolated as a multi-copy suppressor of lysine auxotrophy caused by depletion of copper/zinc-containing superoxide dismutase (CuZn-SOD). Overproduction of Phx1 increased the synthesis of homocitrate synthase, the first enzyme in lysine biosynthetic pathway, which is labile to oxidative stress. Phx1 has a well conserved DNA-binding domain called homeodomain at the N-terminal region and is predicted to be a transcription factor in S. pombe. However, its role has not been revealed in further detail. Here we examined its expression pattern and the phenotype of its null mutant to get clues on its function.
Fluorescence from the Phx1-GFP expressed from a chromosomal fusion gene demonstrated that it is localized primarily in the nucleus, and is distinctly visible during the stationary phase. When we replaced the N-terminal homeobox domain of Phx1 with the DNA binding domain of Pap1, a well-characterized transcription factor, the chimeric protein caused the elevation of transcripts from Pap1-dependent genes such as ctt1+ and trr1+, suggesting that Phx1 possesses transcriptional activating activity when bound to DNA. The amount of phx1+ transcripts sharply increased as cells entered the stationary phase and was maintained at high level throughout the stationary phase. Nutrient shift down to low nitrogen or carbon sources caused phx1+ induction during the exponential phase, suggesting that cells need Phx1 for maintenance function during nutrient starvation. The Δphx1 null mutant showed decreased viability in long-term culture, whereas overproduction of Phx1 increased viability. Decrease in long-term survival was also observed for Δphx1 under N- or C-starved conditions. In addition, Δphx1 mutant was more sensitive to various oxidants and heat shock. When we examined sporulation of the Δphx1/Δphx1 diploid strain, significant decrease in the formation of meiotic spores was observed.
Phx1 is a transcriptional regulator whose synthesis is elevated during stationary phase and by nutrient starvation in S. pombe. It supports long-term survival and stress tolerance against oxidation and heat, and plays a key role in the formation of meiotic spores.
在裂殖酵母 Schizosaccharomyces pombe 中,phx1+(pomb 同源盒)基因最初是作为铜/锌结合超氧化物歧化酶(CuZn-SOD)耗竭引起的赖氨酸营养缺陷型的多拷贝抑制子而被分离出来的。Phx1 的过表达增加了同型柠檬酸合酶的合成,同型柠檬酸合酶是赖氨酸生物合成途径中的第一个酶,易受到氧化应激的影响。Phx1 在 N 端区域具有一个保守的 DNA 结合结构域,称为同源盒结构域,预计在 S. pombe 中是一种转录因子。然而,它的作用尚未进一步详细揭示。在这里,我们检查了它的表达模式和 null 突变体的表型,以获得其功能的线索。
来自染色体融合基因的 Phx1-GFP 的荧光显示,它主要定位于细胞核中,在静止期特别明显。当我们用 Pap1 的 DNA 结合结构域替换 Phx1 的 N 端同源盒结构域时,Pap1 是一种特征明确的转录因子,嵌合蛋白导致 ctt1+和 trr1+等依赖 Pap1 的基因的转录物水平升高,表明 Phx1 与 DNA 结合时具有转录激活活性。当细胞进入静止期时,phx1+转录本的数量急剧增加,并在整个静止期保持高水平。向低氮或碳源的营养物质转移会导致指数期 phx1+的诱导,这表明在营养饥饿期间细胞需要 Phx1 来维持功能。Δphx1 缺失突变体在长期培养中表现出存活能力下降,而过表达 Phx1 则增加了存活能力。在 N 或 C 饥饿条件下,Δphx1 缺失突变体的长期存活能力也下降。此外,Δphx1 突变体对各种氧化剂和热休克更敏感。当我们检查 Δphx1/Δphx1 二倍体菌株的孢子形成时,观察到减数分裂孢子形成的显著减少。
Phx1 是一种转录调节因子,其在 S. pombe 中的合成在静止期和营养饥饿时升高。它支持长期存活和对氧化和热的应激耐受性,并在减数分裂孢子的形成中发挥关键作用。