Human subtelomeric DNA methylation: regulation and roles in telomere function.

Abstract:

:Subtelomeres are the regions at chromosome ends, immediately adjacent to the terminal telomeric repeats. The majority of human subtelomeres are CpG-rich in their distal two kilobases, and are methylated during early embryonic development by the de novo DNA methyltransferase DNMT3B. The biological relevance of subtelomeric DNA methylation is highlighted by the presence of promoters for the long non-coding TERRA transcripts in these CpG-rich regions. Indeed, deviant subtelomeric methylation has been linked with abnormal telomeric phenotypes, as most strikingly found in ICF syndrome. Here we review recent studies that explore new aspects of subtelomeric methylation regulation and demonstrate the significance of maintaining proper DNA methylation at the extreme distal human subtelomeric regions.

journal_name

Curr Opin Genet Dev

authors

Toubiana S,Selig S

doi

10.1016/j.gde.2020.02.004

subject

Has Abstract

pub_date

2020-02-01 00:00:00

pages

9-16

eissn

0959-437X

issn

1879-0380

pii

S0959-437X(20)30007-1

journal_volume

60

pub_type

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