Awate Sanket, Dhar Srijita, Sommers Joshua A, Brosh Robert M
Laboratory of Molecular Gerontology, National Institute on Aging, NIH, NIH Biomedical Research Center, Baltimore, MD, USA.
Methods Mol Biol. 2019;1999:185-207. doi: 10.1007/978-1-4939-9500-4_11.
DNA helicases represent a specialized class of enzymes that play crucial roles in the DNA damage response. Using the energy of nucleoside triphosphate binding and hydrolysis, helicases behave as molecular motors capable of efficiently disrupting the many noncovalent hydrogen bonds that stabilize DNA molecules with secondary structure. In addition to their importance in DNA damage sensing and signaling, DNA helicases facilitate specific steps in DNA repair mechanisms that require polynucleotide tract unwinding or resolution. Because they play fundamental roles in the DNA damage response and DNA repair, defects in helicases disrupt cellular homeostasis. Thus, helicase deficiency or inhibition may result in reduced cell proliferation and survival, apoptosis, DNA damage induction, defective localization of repair proteins to sites of genomic DNA damage, chromosomal instability, and defective DNA repair pathways such as homologous recombination of double-strand breaks. In this chapter, we will describe step-by-step protocols to assay the functional importance of human DNA repair helicases in genome stability and cellular homeostasis.
DNA解旋酶是一类特殊的酶,在DNA损伤反应中发挥着关键作用。利用核苷三磷酸结合和水解的能量,解旋酶充当分子马达,能够有效地破坏许多稳定具有二级结构的DNA分子的非共价氢键。除了在DNA损伤传感和信号传导中的重要性外,DNA解旋酶还促进DNA修复机制中需要解开或解析多核苷酸序列的特定步骤。由于它们在DNA损伤反应和DNA修复中发挥着基本作用,解旋酶的缺陷会破坏细胞内稳态。因此,解旋酶缺乏或抑制可能导致细胞增殖和存活减少、细胞凋亡、DNA损伤诱导、修复蛋白在基因组DNA损伤位点的定位缺陷、染色体不稳定以及诸如双链断裂同源重组等有缺陷的DNA修复途径。在本章中,我们将描述逐步的实验方案,以测定人类DNA修复解旋酶在基因组稳定性和细胞内稳态中的功能重要性。