Bouayadi K, van der Leer-van Hoffen A, Balajee A S, Natarajan A T, van Zeeland A A, Mullenders L H
MGC-Department of Radiation Genetics and Chemical Mutagenesis, Leiden University, Leiden, The Netherlands.
Nucleic Acids Res. 1997 Mar 1;25(5):1056-63. doi: 10.1093/nar/25.5.1056.
In this study the role of nuclear architecture in nucleotide excision repair (NER) was investigated by gentle dismantling of the cell and probing the capability of chromatin to carry out repair in vitro. The rationale behind this approach is that compartmentalization of NER at nuclear structures would make the enzymatic activities refractory to extraction by buffers that solubilize cellular membranes. In order to obtain intact chromatin primary human fibroblasts were encapsulated in agarose microbeads and lysed in isotonic buffers containing the non-ionic detergent Triton X-100. Under these conditions the majority of cellular proteins diffuse out of the beads, but the remaining chromatin is able to replicate and to transcribe DNA in the presence of triphosphates and Mg2+. UV irradiation of confluent repair-proficient human fibroblasts prior to lysis stimulated the incorporation of deoxynucleotide triphosphates in Triton X-100-isolated chromatin, even under stringent lysis conditions. In addition, experiments with UV-sensitive xeroderma pigmentosum (complementation groups A and C) and Cockayne's syndrome fibroblasts (complementation group A) revealed that this repair synthesis was due to global genome repair activity. Transcription-coupled repair was only detectable in cells permeabilized by streptolysin O (SLO). Repair synthesis in Triton X-100-isolated chromatin amounted to 15% of the total repair synthesis as measured in SLO-permeabilized cells. To allow the detection of these activities in vitro, presynthesis complexes have to be formed in intact cells, indicating that chromatin from Triton X-100-lysed cells is unable to initiate NER in vitro. Our data indicate that the components involved in the resynthesis step of NER are tightly associated with chromatin. A substantial fraction of total proliferating cell nuclear antigen (PCNA), which is required for the resynthesis step in NER, has been reported to become Triton X-100 non-extractable and tightly associated with nuclear structures after UV irradiation of cells. We propose that Triton X-100-resistant repair synthesis might be mediated by this chromatin-bound fraction of total PCNA.
在本研究中,通过温和拆解细胞并检测染色质在体外进行修复的能力,来探究核结构在核苷酸切除修复(NER)中的作用。该方法背后的基本原理是,NER在核结构中的区室化会使酶活性难以被溶解细胞膜的缓冲液提取出来。为了获得完整的染色质,将原代人成纤维细胞封装在琼脂糖微珠中,并在含有非离子去污剂 Triton X - 100的等渗缓冲液中裂解。在这些条件下,大多数细胞蛋白从微珠中扩散出来,但剩余的染色质在存在三磷酸核苷酸和Mg2+的情况下能够复制和转录DNA。在裂解之前对汇合的具有修复能力的人成纤维细胞进行紫外线照射,即使在严格的裂解条件下,也能刺激脱氧核苷酸三磷酸在Triton X - 100分离的染色质中的掺入。此外,对紫外线敏感的着色性干皮病(互补组A和C)和科凯恩综合征成纤维细胞(互补组A)的实验表明,这种修复合成是由于全基因组修复活性。转录偶联修复仅在经链球菌溶血素O(SLO)通透的细胞中可检测到。在Triton X - 100分离的染色质中的修复合成量相当于在SLO通透细胞中测得的总修复合成量的15%。为了在体外检测这些活性,必须在完整细胞中形成预合成复合物,这表明来自Triton X - 100裂解细胞的染色质在体外无法启动NER。我们的数据表明,参与NER再合成步骤的成分与染色质紧密相关。据报道,NER再合成步骤所需的增殖细胞核抗原(PCNA)的很大一部分在细胞紫外线照射后变得不可被Triton X - 100提取,并与核结构紧密相关。我们提出,Triton X - 100抗性修复合成可能由总PCNA的这种与染色质结合的部分介导。