Evidence map›Paper›PMID 27836984›Full record

ArticleMolecular biology and evolution2017

Recurrent Innovation at Genes Required for Telomere Integrity in Drosophila.

Yuh Chwen G Lee, Courtney Leek, Mia T Levine

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Cross-species incompatibilities offer new insights into the functional consequences of satellite DNA evolution.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2026
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  16. Establishment and evolution of heterochromatin.Annals of the New York Academy of Sciences · 2020
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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.

Yuh Chwen G LeeDepartment of Ecology and Evolution, University of Chicago, Chicago, IL.
Courtney LeekDepartment of Biology, School of Arts and Sciences, University of Pennsylvania, Philadelphia, PA.
Mia T LevineDepartment of Biology, School of Arts and Sciences, University of Pennsylvania, Philadelphia, PA.

Funding

Evolutionary and functional diversification of chromatin proteinsR00GM107351 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI LEVINE, MIA TAUNA · 2015 to 2017
$727k
Evolutionary and functional diversification of chromatin proteinsK99GM107351 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LEVINE, MIA TAUNA · 2013 to 2014
$180k
The evolution of essential biological functions driven by new genes that reshapeF32GM109676 · NIGMS · UNIVERSITY OF CHICAGO · PI LEE, GRACE YUH CHWEN · 2014 to 2015
$106k
NIGMS NIH HHS F32 GM109676NIGMS NIH HHS K99 GM107351NIGMS NIH HHS R00 GM107351
6 · The paper itself

Abstract

Telomeres are nucleoprotein complexes at the ends of linear chromosomes. These specialized structures ensure genome integrity and faithful chromosome inheritance. Recurrent addition of repetitive, telomere-specific DNA elements to chromosome ends combats end-attrition, while specialized telomere-associated proteins protect naked, double-stranded chromosome ends from promiscuous repair into end-to-end fusions. Although telomere length homeostasis and end-protection are ubiquitous across eukaryotes, there is sporadic but building evidence that the molecular machinery supporting these essential processes evolves rapidly. Nevertheless, no global analysis of the evolutionary forces that shape these fast-evolving proteins has been performed on any eukaryote. The abundant population and comparative genomic resources of Drosophila melanogaster and its close relatives offer us a unique opportunity to fill this gap. Here we leverage population genetics, molecular evolution, and phylogenomics to define the scope and evolutionary mechanisms driving fast evolution of genes required for telomere integrity. We uncover evidence of pervasive positive selection across multiple evolutionary timescales. We also document prolific expansion, turnover, and expression evolution in gene families founded by telomeric proteins. Motivated by the mutant phenotypes and molecular roles of these fast-evolving genes, we put forward four alternative, but not mutually exclusive, models of intra-genomic conflict that may play out at very termini of eukaryotic chromosomes. Our findings set the stage for investigating both the genetic causes and functional consequences of telomere protein evolution in Drosophila and beyond.

Indexed as

AnimalsDNA DamageDNA Transposable ElementsDrosophila melanogasterDrosophila ProteinsEvolution, MolecularFemaleGene DuplicationMaleNuclear ProteinsPhylogenyTelomereDNA Transposable ElementsDrosophila ProteinsNuclear ProteinsDrosophilagene turnoverpositive selectiontelomereterminin.transposable element

Identifiers

PMID27836984
PMCPMC6307840

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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.