Uphoff Stephan, Lord Nathan D, Okumus Burak, Potvin-Trottier Laurent, Sherratt David J, Paulsson Johan
Department of Biochemistry, University of Oxford, Oxford OX1 3QU, UK. Department of Systems Biology, Harvard Medical School, Boston, MA 02115, USA.
Department of Systems Biology, Harvard Medical School, Boston, MA 02115, USA.
Science. 2016 Mar 4;351(6277):1094-7. doi: 10.1126/science.aac9786.
Cells rely on the precise action of proteins that detect and repair DNA damage. However, gene expression noise causes fluctuations in protein abundances that may compromise repair. For the Ada protein in Escherichia coli, which induces its own expression upon repairing DNA alkylation damage, we found that undamaged cells on average produce one Ada molecule per generation. Because production is stochastic, many cells have no Ada molecules and cannot induce the damage response until the first expression event occurs, which sometimes delays the response for generations. This creates a subpopulation of cells with increased mutation rates. Nongenetic variation in protein abundances thus leads to genetic heterogeneity in the population. Our results further suggest that cells balance reliable repair against toxic side effects of abundant DNA repair proteins.
细胞依赖于能够检测和修复DNA损伤的蛋白质的精确作用。然而,基因表达噪声会导致蛋白质丰度的波动,这可能会影响修复过程。对于大肠杆菌中的Ada蛋白,它在修复DNA烷基化损伤时会诱导自身表达,我们发现未受损的细胞平均每代产生一个Ada分子。由于产生过程是随机的,许多细胞没有Ada分子,直到第一次表达事件发生才能诱导损伤反应,这有时会使反应延迟几代。这就产生了一个突变率增加的细胞亚群。因此,蛋白质丰度的非遗传变异导致了群体中的遗传异质性。我们的结果进一步表明,细胞在可靠的修复与大量DNA修复蛋白的毒性副作用之间进行平衡。