Target intelligence / Profile preview

Telomere length regulation protein TEN1 homolog (TEN1)

Target
TEN1
Molecular classification
Telomere maintenance protein, Replication protein A-like complex subunit, DNA-binding protein, Other
01

Overview

TEN1 is a key component of the CST complex (CTC1-STN1-TEN1) responsible for regulating telomere length and facilitating DNA replication at chromosome ends[2][10]. In mammals, TEN1 supports C-strand synthesis after telomerase activity and is critical for telomere duplex replication and genome-wide replication restart[1][6][10]. TEN1 forms a stable protein complex with STN1 and CTC1, with all subunits contributing to telomere homeostasis but playing distinct roles. While CTC1 and STN1 are essential for limiting telomerase activity, TEN1 stabilizes CST complex binding to single-stranded DNA and is required for the fill-in synthesis of the complementary strand[1][6]. Disruption of TEN1 function leads to telomere shortening, chromosomal instability, and compromised cellular proliferation, underscoring its importance in genome maintenance[6][4]. Although highly relevant for fundamental telomere biology and implicated in tumor cell survival mechanisms, TEN1 itself has not been established as a direct therapeutic target.

Other names
TEN1CST complex subunit TEN1C17orf106FLJ39785Telomere length regulation protein TEN1 homologCST complex subunit TEN1, telomerase capping complex subunit homologProtein telomeric pathways with STN1 homologTelomeric pathways in association with Stn1, number 1
02

Biological functions

Telomere length regulation[3][1][4]C-strand (complementary strand) synthesis after telomerase activity[1][6][10]Genome-wide replication restart after fork stalling[6]Telomere and chromosome end protection[3][6]
03

Disease associations

Cancer (particularly in the context of telomere maintenance; dysfunction can lead to genomic instability in cancer cells)[4][6]Other (general chromosomal and replicative stress responses)
04

Safety considerations

Genomic instability with loss or depletion (delays in overhang shortening, telomere loss, fragility, multinucleation, increased anaphase bridges)[6][4]Therapeutic targeting not established; thus, related safety concerns are theoretical or research-based
05

Biomarkers

Telomere length (TEN1 and CST complex expression can be associated with telomere length in research settings)[5]Presence of C-circles/t-circles in ALT (Alternative Lengthening of Telomeres) cancer cells[4]

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