Evidence map›Paper›PMID 31434740›Full record

ReviewThe Journal of biological chemistry2019

Back to the future: The intimate and evolving connection between telomere-related factors and genotoxic stress.

Borja Barbero Barcenilla, Dorothy E Shippen

Abstract readReview
In one paragraph

Review in The Journal of biological chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Quantification of 8-International journal of molecular sciences · 2022
    Article
  7. Article
  8. 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

2 authors.

Borja Barbero BarcenillaDepartment of Biochemistry and Biophysics, Texas A&M University, College Station, Texas 77843-2128.
Dorothy E ShippenDepartment of Biochemistry and Biophysics, Texas A&M University, College Station, Texas 77843-2128 dshippen@tamu.edu.

Funding

Telomere Structure and Function in ArabidopsisR01GM065383 · NIGMS · TEXAS A&M UNIVERSITY SYSTEM · PI SHIPPEN, DOROTHY · 2002 to 2023
$6.8M
Genetic and epigenetic architecture of natural telomere length variationR01GM127402 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI SHAKIROV, EUGENE V · 2018 to 2025
$2.4M
NIGMS NIH HHS R01 GM065383NIGMS NIH HHS R01 GM127402
6 · The paper itself

Abstract

The conversion of circular genomes to linear chromosomes during molecular evolution required the invention of telomeres. This entailed the acquisition of factors necessary to fulfill two new requirements: the need to fully replicate terminal DNA sequences and the ability to distinguish chromosome ends from damaged DNA. Here we consider the multifaceted functions of factors recruited to perpetuate and stabilize telomeres. We discuss recent theories for how telomere factors evolved from existing cellular machineries and examine their engagement in nontelomeric functions such as DNA repair, replication, and transcriptional regulation. We highlight the remarkable versatility of protection of telomeres 1 (POT1) proteins that was fueled by gene duplication and divergence events that occurred independently across several eukaryotic lineages. Finally, we consider the relationship between oxidative stress and telomeres and the enigmatic role of telomere-associated proteins in mitochondria. These findings point to an evolving and intimate connection between telomeres and cellular physiology and the strong drive to maintain chromosome integrity.

Indexed as

DNA DamageDNA RepairEukaryotic CellsGene Expression RegulationHumansMitochondriaOxidative StressShelterin ComplexTelomeraseTelomereTelomere-Binding ProteinsPOT1 protein, humanShelterin ComplexTelomeraseTelomere-Binding Proteinschromosome endsCSTDNA replicationgenome integritymolecular evolutionoxidative damagePOT1protection Of telomeres 1shelterintelomerasetelomerase reverse transcriptase (TERT)telomere repeat

Identifiers

PMID31434740
PMCPMC6779425

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.