Huang Jing, Gali Himabindu, Gichimu Julia, Bellani Marina A, Pokharel Durga, Paramasivam Manikandan, Seidman Michael M
Laboratory of Molecular Gerontology, National Institute on Aging, National Institutes of Health.
Laboratory of Molecular Gerontology, National Institute on Aging, National Institutes of Health;
J Vis Exp. 2017 Apr 20(122):55541. doi: 10.3791/55541.
The DNA Damage Response (DDR) has been extensively characterized in studies of double strand breaks (DSBs) induced by laser micro beam irradiation in live cells. The DDR to helix distorting covalent DNA modifications, including interstrand DNA crosslinks (ICLs), is not as well defined. We have studied the DDR stimulated by ICLs, localized by laser photoactivation of immunotagged psoralens, in the nuclei of live cells. In order to address fundamental questions about adduct distribution and replication fork encounters, we combined laser localization with two other technologies. DNA fibers are often used to display the progress of replication forks by immunofluorescence of nucleoside analogues incorporated during short pulses. Immunoquantum dots have been widely employed for single molecule imaging. In the new approach, DNA fibers from cells carrying laser localized ICLs are spread onto microscope slides. The tagged ICLs are displayed with immunoquantum dots and the inter-lesion distances determined. Replication fork collisions with ICLs can be visualized and different encounter patterns identified and quantitated.
在活细胞中,通过激光微束照射诱导双链断裂(DSB)的研究对DNA损伤反应(DDR)进行了广泛的表征。对包括链间DNA交联(ICL)在内的螺旋扭曲共价DNA修饰的DDR尚未明确界定。我们研究了由免疫标记补骨脂素的激光光活化定位的ICL在活细胞核中刺激的DDR。为了解决有关加合物分布和复制叉相遇的基本问题,我们将激光定位与其他两种技术相结合。DNA纤维常用于通过短脉冲期间掺入的核苷类似物的免疫荧光来显示复制叉的进展。免疫量子点已广泛用于单分子成像。在新方法中,将携带激光定位ICL的细胞的DNA纤维铺展在显微镜载玻片上。用免疫量子点显示标记的ICL,并确定损伤间距离。可以观察到复制叉与ICL的碰撞,并识别和定量不同的相遇模式。