Department of Bacteriology, University of Wisconsin-Madison, Madison, WI, USA.
Department of Bacteriology, University of Wisconsin-Madison, Madison, WI, USA.
J Mol Biol. 2021 Sep 17;433(19):167189. doi: 10.1016/j.jmb.2021.167189. Epub 2021 Aug 10.
Primase is an essential component of the DNA replication machinery, responsible for synthesizing RNA primers that initiate leading and lagging strand DNA synthesis. Bacterial primase activity can be regulated by the starvation-inducible nucleotide (p)ppGpp. This regulation contributes to a timely inhibition of DNA replication upon amino acid starvation in the Gram-positive bacterium Bacillus subtilis. Here, we characterize the effect of (p)ppGpp on B. subtilis DnaG primase activity in vitro. Using a single-nucleotide resolution primase assay, we dissected the effect of ppGpp on the initiation, extension, and fidelity of B. subtilis primase. We found that ppGpp has a mild effect on initiation, but strongly inhibits primer extension and reduces primase processivity, promoting termination of primer extension. High (p)ppGpp concentration, together with low GTP concentration, additively inhibit primase activity. This explains the strong inhibition of replication elongation during starvation which induces high levels of (p)ppGpp and depletion of GTP in B. subtilis. Finally, we found that lowering GTP concentration results in mismatches in primer base pairing that allow priming readthrough, and that ppGpp reduces readthrough to protect priming fidelity. These results highlight the importance of (p)ppGpp in protecting replisome integrity and genome stability in fluctuating nucleotide concentrations upon onset of environmental stress.
引物酶是 DNA 复制机器的重要组成部分,负责合成起始前导链和滞后链 DNA 合成的 RNA 引物。细菌引物酶活性可以通过饥饿诱导的核苷酸(p)ppGpp 进行调节。这种调节有助于在革兰氏阳性细菌枯草芽孢杆菌中氨基酸饥饿时及时抑制 DNA 复制。在这里,我们在体外表征了(p)ppGpp 对枯草芽孢杆菌 DnaG 引物酶活性的影响。使用单核苷酸分辨率引物酶测定法,我们剖析了 ppGpp 对枯草芽孢杆菌引物酶起始、延伸和保真度的影响。我们发现 ppGpp 对起始有轻微影响,但强烈抑制引物延伸并降低引物酶的进程性,促进引物延伸终止。高(p)ppGpp 浓度与低 GTP 浓度一起,附加抑制引物酶活性。这解释了在诱导高浓度(p)ppGpp 和枯草芽孢杆菌 GTP 耗尽的饥饿期间强烈抑制复制延伸的原因。最后,我们发现降低 GTP 浓度会导致引物碱基配对产生错配,从而允许引物通读,并发现 ppGpp 降低通读以保护引物保真度。这些结果强调了(p)ppGpp 在保护复制体完整性和基因组稳定性方面的重要性,特别是在环境压力开始时核苷酸浓度波动的情况下。