Department of Biochemistry and Molecular Genetics, University of Virginia Health System, School of Medicine, Jordan Hall, Box 800733, Charlottesville, VA 22908, USA.
Mol Cell Biol. 2010 Jul;30(13):3329-41. doi: 10.1128/MCB.01590-09. Epub 2010 May 3.
Genes encoding thiamine biosynthesis enzymes in microorganisms are tightly regulated such that low environmental thiamine concentrations activate transcription and high concentrations are repressive. We have determined that multiple thiamine (THI) genes in Saccharomyces cerevisiae are also regulated by the intracellular NAD(+) concentration via the NAD(+)-dependent histone deacetylase (HDAC) Hst1 and, to a lesser extent, Sir2. Both of these HDACs associate with a distal region of the affected THI gene promoters that does not overlap with a previously defined enhancer region bound by the thiamine-responsive Thi2/Thi3/Pdc2 transcriptional activators. The specificity of histone H3 and/or H4 deacetylation carried out by Hst1 and Sir2 at the distal promoter region depends on the THI gene being tested. Hst1/Sir2-mediated repression of the THI genes occurs at the level of basal expression, thus representing the first set of transcription factors shown to actively repress this gene class. Importantly, lowering the NAD(+) concentration and inhibiting the Hst1/Sum1 HDAC complex elevated the intracellular thiamine concentration due to increased thiamine biosynthesis and transport, implicating NAD(+) in the control of thiamine homeostasis.
在微生物中,编码硫胺素生物合成酶的基因受到严格调控,使得低环境硫胺素浓度激活转录,而高浓度则具有抑制作用。我们已经确定,酿酒酵母中的多个硫胺素(THI)基因也通过细胞内 NAD(+)浓度被 NAD(+)依赖性组蛋白去乙酰化酶(HDAC)Hst1 调控,在较小程度上还被 Sir2 调控。这两种 HDAC 都与受影响的 THI 基因启动子的远端区域结合,该区域不与先前定义的由硫胺素反应性 Thi2/Thi3/Pdc2 转录激活物结合的增强子区域重叠。Hst1 和 Sir2 在远端启动子区域进行的组蛋白 H3 和/或 H4 去乙酰化的特异性取决于所测试的 THI 基因。Hst1/Sir2 介导的 THI 基因的抑制发生在基础表达水平,因此代表了第一组被证明可主动抑制该基因类别的转录因子。重要的是,降低 NAD(+)浓度并抑制 Hst1/Sum1 HDAC 复合物会由于增加硫胺素生物合成和运输而提高细胞内硫胺素浓度,这表明 NAD(+)参与了硫胺素动态平衡的控制。