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Cell Rep. 2012 Nov 29;2(5):1096-103. doi: 10.1016/j.celrep.2012.10.007. Epub 2012 Nov 8.

Human CST has independent functions during telomere duplex replication and C-strand fill-in.

Author information

1
Department of Cancer and Cell Biology, University of Cincinnati, Cincinnati, OH 45267-0521, USA.

Abstract

Human CST (CTC1-STN1-TEN1) is an RPA-like complex that is needed for efficient replication through the telomere duplex and genome-wide replication restart after fork stalling. Here, we show that STN1/CST has a second function in telomere replication during G-overhang maturation. Analysis of overhang structure after STN1 depletion revealed normal kinetics for telomerase-mediated extension in S phase but a delay in subsequent overhang shortening. This delay resulted from a defect in C-strand fill-in. Short telomeres exhibited the fill-in defect but normal telomere duplex replication, indicating that STN1/CST functions independently in these processes. Our work also indicates that the requirement for STN1/CST in telomere duplex replication correlates with increasing telomere length and replication stress. Our results provide direct evidence that STN1/CST participates in C-strand fill-in. They also demonstrate that STN1/CST participates in two mechanistically separate steps during telomere replication and identify CST as a replication factor that solves diverse replication-associated problems.

PMID:
23142664
PMCID:
PMC3513692
DOI:
10.1016/j.celrep.2012.10.007
[Indexed for MEDLINE]
Free PMC Article

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