Zanella Elia, Doksani Ylli
IFOM ETS, The AIRC Institute of Molecular Oncology, 20139 Milan, Italy.
IFOM ETS, The AIRC Institute of Molecular Oncology, 20139 Milan, Italy
Cold Spring Harb Perspect Biol. 2025 Mar 17. doi: 10.1101/cshperspect.a041694.
Telomeric repeats recruit the shelterin complex to prevent activation of the double-strand break response at chromosome ends. Thousands of TTAGGG repeats are present at each chromosome end to ensure telomere function. This abundance of G-rich repeats comes with the propensity to generate unusual DNA structures. The telomere loop (t-loop) structure, generated by strand invasion of the 3' overhang in the internal repeats, contributes to telomere function. G4-DNA is promoted by the stretches of G-rich repeats in a single-stranded form and may affect telomere replication and elongation by telomerase. The intramolecular homology can lead to the formation of internal loops (i-loops) via intramolecular recombination at sites of telomeric damage, which can promote the excision of telomeric repeats as extrachromosomal circular DNA. Shelterin promotes t-loops, counteracting the accumulation of pathological structures either directly or via the recruitment of specialized helicases. Here, we will discuss the current evidence for the formation of unusual DNA structures at telomeres and possible implications for telomere function.
端粒重复序列招募端粒保护蛋白复合体,以防止染色体末端的双链断裂反应被激活。每条染色体末端都存在数千个TTAGGG重复序列,以确保端粒功能。这种富含G的重复序列的丰富性伴随着产生异常DNA结构的倾向。由内部重复序列中3'突出端的链侵入产生的端粒环(t-loop)结构有助于端粒功能。单链形式的富含G的重复序列延伸促进了G4-DNA的形成,并且可能影响端粒酶介导的端粒复制和延伸。分子内同源性可通过端粒损伤位点的分子内重组导致内部环(i-loop)的形成,这可促进端粒重复序列作为染色体外环状DNA的切除。端粒保护蛋白复合体促进t环的形成,直接或通过招募专门的解旋酶来对抗病理结构的积累。在这里,我们将讨论目前关于端粒处异常DNA结构形成的证据以及对端粒功能的可能影响。