Evidence map›Paper›PMID 28650257›Full record

ArticleCell cycle (Georgetown, Tex.)2017

Sequential phosphorylation of CST subunits by different cyclin-Cdk1 complexes orchestrate telomere replication.

Veena Gopalakrishnan, Cherylin Ruiling Tan, Shang Li

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 21 citations in OpenAlex.

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  13. Emerging roles of CST in maintaining genome stability and human disease.Frontiers in bioscience (Landmark edition) · 2018
    Review
  14. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Veena Gopalakrishnana Program in Cancer and Stem Cell Biology , Duke-NUS Medical School , Singapore.
Cherylin Ruiling Tanb Department of Biological Sciences , National University of Singapore , Singapore.
Shang Lia Program in Cancer and Stem Cell Biology , Duke-NUS Medical School , Singapore.
Duke-NUS Medical School · SGNational University of Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Telomeres are nucleoprotein structures that cap the ends of linear chromosomes. Telomere homeostasis is central to maintaining genomic integrity. In budding yeast, Cdk1 phosphorylates the telomere-specific binding protein, Cdc13, promoting the recruitment of telomerase to telomere and thereby telomere elongation. Cdc13 is also an integral part of the CST (Cdc13-Stn1-Ten1) complex that is essential for telomere capping and counteracting telomerase-dependent telomere elongation. Therefore, telomere length homeostasis is a balance between telomerase-extendable and CST-unextendable states. In our earlier work, we showed that Cdk1 also phosphorylates Stn1 which occurs sequentially following Cdc13 phosphorylation during cell cycle progression. This stabilizes the CST complex at the telomere and results in telomerase inhibition. Hence Cdk1-dependent phosphorylations of Stn1 acts like a molecular switch that drives Cdc13 to complex with Stn1-Ten1 rather than with telomerase. However, the underlying mechanism of how a single cyclin-dependent kinase phosphorylates Cdc13 and Stn1 in temporally distinct windows is largely unclear. Here, we show that S phase cyclins are necessary for telomere maintenance. The S phase and mitotic cyclins facilitate Cdc13 and Stn1 phosphorylation respectively, to exert opposing outcomes at the telomere. Thus, our results highlight a previously unappreciated role for cyclins in telomere replication.

Indexed as

CDC2 Protein KinaseCell Cycle ProteinsChromosomal Proteins, Non-HistoneCyclin BCyclinsDNA ReplicationMutagenesisPhosphorylationProteolysisSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsS PhaseTelomeraseTelomereTelomere-Binding ProteinsTelomere ShorteningCdc13 protein, S cerevisiaeCDC2 Protein KinaseCell Cycle ProteinsChromosomal Proteins, Non-HistoneCLB2 protein, S cerevisiaeCLB5 protein, S cerevisiaeCLB6 protein, S cerevisiaeCyclin BCyclinsSaccharomyces cerevisiae ProteinsStn1 protein, S cerevisiaeTelomeraseTelomere-Binding ProteinsTEN1 protein, S cerevisiaeBudding yeastCdk1cell cycleCST complexcyclinsphosphorylationtelomere

Identifiers

PMID28650257
PMCPMC5531626
OpenAlexW2682996847

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.