METTL3-mediated m6A modification stabilizes TERRA and maintains telomere stability

Telomeric repeat-containing RNA (TERRA) is a type of long non-coding RNA transcribed from telomeres, and it forms R-loops by invasion into telomeric DNA. Since either an excessive or inadequate number of R-loops leads to telomere instability, the TERRA levels need to be delicately modulated. In this study, we found that m(6)A modification presents on the subtelomeric regions of TERRA and stabilizes it, and the loss of METTL3 impacts telomere stability. Mechanically, the m(6)A modification on TERRA is catalyzed by METTL3, recognized and stabilized by the m(6)A reader YTHDC1. Knockdown of either METTL3 or YTHDC1 enhances TERRA degradation. The m(6)A-modified TERRA forms R-loops and promotes homologous recombination which is essential for the alternative lengthening of telomeres (ALT) pathway in cancer cells. METTL3 depletion leads to R-loop reduction, telomere shortening and instability. Altogether, these findings reveal that METTL3 protects telomeres by catalyzing m(6)A modification on TERRA, indicating that inhibition or deletion of METTL3 is potentially a new avenue for ALT cancer therapy.

Automated summary

This study reveals the role of m(6)A modification in protecting telomere stability. METTL3 catalyzes m(6)A modification on TERRA, stabilizing its structure and promoting the ALT pathway. Depletion of METTL3 leads to reduced R-loops, telomere shortening, and instability.