Lee Junyeop, Lee Jina, Sohn Eric J, Taglialatela Angelo, O'Sullivan Roderick J, Ciccia Alberto, Min Jaewon
Institute for Cancer Genetics, Columbia University Vagelos College of Physicians and Surgeons, New York, NY, USA.
Department of Pathology and Cell Biology, Columbia University Vagelos College of Physicians and Surgeons, New York, NY, USA.
bioRxiv. 2023 Oct 23:2023.07.31.551186. doi: 10.1101/2023.07.31.551186.
Alternative Lengthening of Telomeres (ALT) is a telomere maintenance mechanism mediated by break-induced replication (BIR), evident in approximately 15% of human cancers. A characteristic feature of ALT cancers is the presence of C-circles, circular single-stranded telomeric DNAs composed of C-rich sequences. Despite the fact that extrachromosomal C-rich single-stranded DNAs (ssDNAs), unique to ALT cells, are considered potential precursors of C-circles, their generation process remains undefined. Here, we introduce a highly sensitive method to detect single stranded telomeric DNA, called 4SET (Strand-Specific Southern-blot for Single-stranded Extrachromosomal Telomeres) assay. Utilizing 4SET, we are able to capture C-rich single stranded DNAs that are near 200 to 1500 nucleotides in size. Both linear C-rich ssDNAs and C-circles are abundant in the fractions of cytoplasm and nucleoplasm, which supports the idea that linear C-rich ssDNA accumulation may indeed precede C-circle formation. We also found that C-rich ssDNAs originate during Okazaki fragment processing during lagging strand DNA synthesis. The generation of C-rich ssDNA requires CST-PP (CTC1/STN1/TEN1-PRIMASE-Polymerase alpha) complex-mediated priming of the C-strand DNA synthesis and subsequent excessive strand displacement of the C-rich strand mediated by the DNA Polymerase delta and the BLM helicase. Our work proposes a new model for the generation of C-rich ssDNAs and C-circles during ALT-mediated telomere elongation.
端粒替代延长(ALT)是一种由断裂诱导复制(BIR)介导的端粒维持机制,在大约15%的人类癌症中很明显。ALT癌症的一个特征是存在C环,即由富含C的序列组成的环状单链端粒DNA。尽管ALT细胞特有的染色体外富含C的单链DNA(ssDNA)被认为是C环的潜在前体,但其产生过程仍不清楚。在这里,我们介绍了一种检测单链端粒DNA的高灵敏度方法,称为4SET(单链染色体外端粒的链特异性Southern印迹)分析。利用4SET,我们能够捕获大小在200到1500个核苷酸之间的富含C的单链DNA。线性富含C的ssDNA和C环在细胞质和核质部分都很丰富,这支持了线性富含C的ssDNA积累确实可能先于C环形成的观点。我们还发现,富含C的ssDNA在滞后链DNA合成过程中的冈崎片段加工过程中产生。富含C的ssDNA的产生需要CST-PP(CTC1/STN1/TEN1-引发酶-聚合酶α)复合物介导的C链DNA合成引发,以及随后由DNA聚合酶δ和BLM解旋酶介导的富含C的链的过度链置换。我们的工作提出了一种在ALT介导的端粒延长过程中产生富含C的ssDNA和C环的新模型。