Protection of the Telomeric Junction by the Shelterin Complex

Shelterin serves critical roles in suppressing superfluous DNA damage repair pathways on telomeres. The junction between double-stranded telomeric tracts (dsTEL) and single-stranded telomeric overhang (ssTEL) is the most accessible region of the telomeric DNA. The shelterin complex contains dsTEL and ssTEL binding proteins and can protect this junction by bridging the ssTEL and dsTEL tracts. To test this possibility, we monitored shelterin binding to telomeric DNA substrates with varying ssTEL and dsTEL lengths and quantified its impact on telomere accessibility using single-molecule fluorescence microscopy methods <i>in vitro</i>. We identified the first dsTEL repeat nearest the junction as the preferred binding site for creating the shelterin bridge. Shelterin requires at least two ssTEL repeats, while the POT1 subunit of shelterin that binds to ssTEL requires longer ssTEL tracts for stable binding to telomeres and effective protection of the junction region. The ability of POT1 to protect the junction is significantly enhanced by the 5'-phosphate at the junction. Collectively, our results show that shelterin enhances the binding stability of POT1 to ssTEL and provides more effective protection compared with POT1 alone by bridging single- and double-stranded telomeric tracts.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2024-08-29
DOI
https://doi.org/10.1021/jacs.4c08649
Citations
4
Primary Topic
Telomeres, Telomerase, and Senescence
Type
article
Field-Weighted Citation Impact
1.31

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article

Protection of the Telomeric Junction by the Shelterin Complex

Sajad Shiekh, Amanda Jack, Sineth G. Kodikara, Hamza Balci et al.
4 citations
Journal of the American Chemical Society
Telomeres, Telomerase, and Senescence
1.31
article

Protection of the Telomeric Junction by the Shelterin Complex

Sajad Shiekh, Amanda Jack, Sineth G. Kodikara, Hamza Balci, Ahmet Yıldız, Darion Feldt, Janan Alfehaid, Sabaha Pasha
article en
4 citations

Abstract

Shelterin serves critical roles in suppressing superfluous DNA damage repair pathways on telomeres. The junction between double-stranded telomeric tracts (dsTEL) and single-stranded telomeric overhang (ssTEL) is the most accessible region of the telomeric DNA. The shelterin complex contains dsTEL and ssTEL binding proteins and can protect this junction by bridging the ssTEL and dsTEL tracts. To test this possibility, we monitored shelterin binding to telomeric DNA substrates with varying ssTEL and dsTEL lengths and quantified its impact on telomere accessibility using single-molecule fluorescence microscopy methods <i>in vitro</i>. We identified the first dsTEL repeat nearest the junction as the preferred binding site for creating the shelterin bridge. Shelterin requires at least two ssTEL repeats, while the POT1 subunit of shelterin that binds to ssTEL requires longer ssTEL tracts for stable binding to telomeres and effective protection of the junction region. The ability of POT1 to protect the junction is significantly enhanced by the 5'-phosphate at the junction. Collectively, our results show that shelterin enhances the binding stability of POT1 to ssTEL and provides more effective protection compared with POT1 alone by bridging single- and double-stranded telomeric tracts.

Journal of the American Chemical SocietyVol. 146(36)
Kent State University (US), University of California System (US), University of California, Berkeley (US)
National Science Foundation, Kent State University, Northern Border University, National Institutes of Health
Openalex Percentile: Top 19%
Telomeres, Telomerase, and Senescence
1.31
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Protection of the Telomeric Junction by the Shelterin Complex — Sajad Shiekh, Amanda Jack, et al. · Journal of the American Chemical Society (2024) | TGRS Research Map | TGRS