Cell Biology and Epigenetics, Department of Biology, Technical University of Darmstadt, 64287 Darmstadt, Germany.
Biophysics Department, GSI Helmholtzzentrum für Schwerionenforschung GmbH, 64291 Darmstadt, Germany.
Int J Mol Sci. 2022 Mar 31;23(7):3896. doi: 10.3390/ijms23073896.
CTCF is a nuclear protein initially discovered for its role in enhancer-promoter insulation. It has been shown to play a role in genome architecture and in fact, its DNA binding sites are enriched at the borders of chromatin domains. Recently, we showed that depletion of CTCF impairs the DNA damage response to ionizing radiation. To investigate the relationship between chromatin domains and DNA damage repair, we present here clonogenic survival assays in different cell lines upon CTCF knockdown and ionizing irradiation. The application of a wide range of ionizing irradiation doses (0-10 Gy) allowed us to investigate the survival response through a biophysical model that accounts for the double-strand breaks' probability distribution onto chromatin domains. We demonstrate that the radiosensitivity of different cell lines is increased upon lowering the amount of the architectural protein. Our model shows that the deficiency in the DNA repair ability is related to the changes in the size of chromatin domains that occur when different amounts of CTCF are present in the nucleus.
CTCF 是一种核蛋白,最初因其在增强子-启动子隔离中的作用而被发现。现已表明其在基因组结构中发挥作用,实际上,其 DNA 结合位点在染色质域的边界处富集。最近,我们表明 CTCF 的耗竭会损害电离辐射的 DNA 损伤反应。为了研究染色质域与 DNA 损伤修复之间的关系,我们在此展示了在 CTCF 敲低和电离辐射后不同细胞系中的集落形成存活测定。应用广泛的电离辐射剂量(0-10Gy)使我们能够通过考虑双链断裂在染色质域上的概率分布的生物物理模型来研究存活反应。我们证明,降低结构蛋白的数量会增加不同细胞系的放射敏感性。我们的模型表明,当细胞核中存在不同数量的 CTCF 时,染色质域大小的变化与 DNA 修复能力的缺陷有关。