Unknown

Dataset Information

0

TERRA G-quadruplex RNA interaction with TRF2 GAR domain is required for telomere integrity.


ABSTRACT: Telomere dysfunction causes chromosomal instability which is associated with many cancers and age-related diseases. The non-coding telomeric repeat-containing RNA (TERRA) forms a structural and regulatory component of the telomere that is implicated in telomere maintenance and chromosomal end protection. The basic N-terminal Gly/Arg-rich (GAR) domain of telomeric repeat-binding factor 2 (TRF2) can bind TERRA but the structural basis and significance of this interaction remains poorly understood. Here, we show that TRF2 GAR recognizes G-quadruplex features of TERRA. We show that small molecules that disrupt the TERRA-TRF2 GAR complex, such as N-methyl mesoporphyrin IX (NMM) or genetic deletion of TRF2 GAR domain, result in the loss of TERRA, and the induction of ?H2AX-associated telomeric DNA damage associated with decreased telomere length, and increased telomere aberrations, including telomere fragility. Taken together, our data indicates that the G-quadruplex structure of TERRA is an important recognition element for TRF2 GAR domain and this interaction between TRF2 GAR and TERRA is essential to maintain telomere stability.

SUBMITTER: Mei Y 

PROVIDER: S-EPMC7876106 | biostudies-literature | 2021 Feb

REPOSITORIES: biostudies-literature

altmetric image

Publications

TERRA G-quadruplex RNA interaction with TRF2 GAR domain is required for telomere integrity.

Mei Yang Y   Deng Zhong Z   Vladimirova Olga O   Gulve Nitish N   Johnson F Brad FB   Drosopoulos William C WC   Schildkraut Carl L CL   Lieberman Paul M PM  

Scientific reports 20210210 1


Telomere dysfunction causes chromosomal instability which is associated with many cancers and age-related diseases. The non-coding telomeric repeat-containing RNA (TERRA) forms a structural and regulatory component of the telomere that is implicated in telomere maintenance and chromosomal end protection. The basic N-terminal Gly/Arg-rich (GAR) domain of telomeric repeat-binding factor 2 (TRF2) can bind TERRA but the structural basis and significance of this interaction remains poorly understood.  ...[more]

Similar Datasets

| S-EPMC5449629 | biostudies-literature
| S-EPMC3655473 | biostudies-literature
| S-EPMC10711441 | biostudies-literature
| S-EPMC2749977 | biostudies-literature
2021-04-21 | MSV000087276 | MassIVE
| S-EPMC3528108 | biostudies-literature
| S-EPMC8213692 | biostudies-literature
| S-EPMC7611063 | biostudies-literature
| S-EPMC9147070 | biostudies-literature
| S-EPMC2938214 | biostudies-literature