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Reference - PMID:29167439 - Eroded telomeres are rearranged in quiescent fission yeast cells through duplications of subtelomeric sequences.

Reference summary

PubMed ID
PMID:29167439
Title
Eroded telomeres are rearranged in quiescent fission yeast cells through duplications of subtelomeric sequences.
Authors
Maestroni L, Audry J, Matmati S, Arcangioli B, Géli V, Coulon S
Citation
Nat Commun 2017 Nov 22;8(1):1684
Publication year
2017
Abstract
While the mechanisms of telomere maintenance has been investigated in dividing cells, little is known about the stability of telomeres in quiescent cells and how dysfunctional telomeres are processed in non-proliferating cells. Here we examine the stability of telomeres in quiescent cells using fission yeast. While wild type telomeres are stable in quiescence, we observe that eroded telomeres were highly rearranged during quiescence in telomerase minus cells. These rearrangements depend on homologous recombination (HR) and correspond to duplications of subtelomeric regions. HR is initiated at newly identified subtelomeric homologous repeated sequences (HRS). We further show that TERRA (Telomeric Repeat-containing RNA) is increased in post-mitotic cells with short telomeres and correlates with telomere rearrangements. Finally, we demonstrate that rearranged telomeres prevent cells to exit properly from quiescence. Taken together, we describe in fission yeast a mode of telomere repair mechanism specific to post-mitotic cells that is likely promoted by transcription.

Annotation

Multi-locus phenotype

FYPO:0006507 - increased subtelomeric DNA amplification during G0

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FYPO:0006518 - loss of viability in G0

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Single locus phenotype

FYPO:0002955 - abnormal G0 to G1 transition

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FYPO:0002945 - increased RNA level during G0

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FYPO:0006507 - increased subtelomeric DNA amplification during G0

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