Kyriacou Eftychia, Lingner Joachim
Swiss Institute for Experimental Cancer Research (ISREC), School of Life Sciences, École Polytechnique Fédérale de Lausanne (EPFL), 1015 Lausanne, Switzerland.
Curr Opin Cell Biol. 2024 Dec;91:102437. doi: 10.1016/j.ceb.2024.102437. Epub 2024 Sep 28.
TERRA long noncoding RNAs play key roles in telomere function and maintenance. They can orchestrate telomeric chromatin remodeling, regulate telomere maintenance by telomerase and homology-directed repair, and they participate in the telomeric DNA damage response. TERRA associates with chromosome ends through base-pairing forming R-loops, which are mediated by the RAD51 DNA recombinase and its partner RAD51AP1. Telomeric R-loops interfere with replication fork progression, stimulating a switch of telomere maintenance from semiconservative DNA replication to homology-directed repair (HDR). The latter mechanism is exploited by a subset of cancer cells that lack telomerase, referred to as ALT. In addition, TERRA stimulates HDR at short telomeres during aging, delaying cellular senescence. During carcinogenesis, when cells with eroded telomeres enter replicative crisis, TERRA acts as a signaling molecule to mediate autophagic cell death.
端粒重复序列RNA(TERRA)长链非编码RNA在端粒功能和维持中发挥关键作用。它们可以协调端粒染色质重塑,通过端粒酶和同源定向修复来调节端粒维持,并且参与端粒DNA损伤反应。TERRA通过碱基配对形成R环与染色体末端结合,这由RAD51 DNA重组酶及其伴侣RAD51AP1介导。端粒R环干扰复制叉的进展,刺激端粒维持从半保留DNA复制转变为同源定向修复(HDR)。后一种机制被一部分缺乏端粒酶的癌细胞所利用,即所谓的端粒延长替代途径(ALT)。此外,TERRA在衰老过程中刺激短端粒处的HDR,延迟细胞衰老。在致癌过程中,当端粒受损的细胞进入复制危机时,TERRA作为信号分子介导自噬性细胞死亡。