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端粒重复序列RNA(TERRA)与端粒的替代延长:一件危险的事。

TERRA and the alternative lengthening of telomeres: a dangerous affair.

作者信息

Azzalin Claus M

机构信息

Instituto de Medicina Molecular João Lobo Antunes (iMM), Faculdade de Medicina da Universidade de Lisboa, Portugal.

出版信息

FEBS Lett. 2025 Jan;599(2):157-165. doi: 10.1002/1873-3468.14844. Epub 2024 Mar 6.

Abstract

Eukaryotic telomeres are transcribed into the long noncoding RNA TERRA. A fraction of TERRA remains associated with telomeres by forming RNA:DNA hybrids dubbed telR-loops. TERRA and telR-loops are essential to promote telomere elongation in human cancer cells that maintain telomeres through a homology-directed repair pathway known as alternative lengthening of telomeres or ALT. However, TERRA and telR-loops compromise telomere integrity and cell viability if their levels are not finely tuned. The study of telomere transcription in ALT cells will enormously expand our understanding of the ALT mechanism and of how genome integrity is maintained. Moreover, telomere transcription, TERRA and telR-loops are likely to become exceptionally suited targets for the development of novel anti-cancer therapies.

摘要

真核生物端粒被转录成长链非编码RNA TERRA。一部分TERRA通过形成被称为telR环的RNA:DNA杂交体而与端粒保持关联。TERRA和telR环对于通过一种称为端粒替代延长(ALT)的同源性定向修复途径维持端粒的人类癌细胞中端粒延长至关重要。然而,如果TERRA和telR环的水平未得到精细调控,它们会损害端粒完整性和细胞活力。对ALT细胞中端粒转录的研究将极大地扩展我们对ALT机制以及基因组完整性如何维持的理解。此外,端粒转录、TERRA和telR环很可能成为新型抗癌疗法开发的特别合适的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e5/11771730/e2c365d91d52/FEB2-599-157-g002.jpg

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