Evidence map›Paper›PMID 29514101›Full record

ArticleCell reports2018

Accelerated Evolution in Distinctive Species Reveals Candidate Elements for Clinically Relevant Traits, Including Mutation and Cancer Resistance.

Elliott Ferris, Lisa M Abegglen, Joshua D Schiffman, Christopher Gregg

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
7.4field-weighted citation impact, top 4% 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

31 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Indirect genomic effects shape cancer risk across species.bioRxiv : the preprint server for biology · 2026
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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

4 authors at 2 institutions in 1 country.

Elliott FerrisDepartment of Neurobiology and Anatomy, University of Utah, Salt Lake City, UT 84132-3401, USA.
Lisa M AbegglenDepartment of Pediatrics, University of Utah, Salt Lake City, UT 84132-3401, USA; Huntsman Cancer Institute, Salt Lake City, UT, USA.
Joshua D SchiffmanDepartment of Pediatrics, University of Utah, Salt Lake City, UT 84132-3401, USA; Department of Oncological Sciences, University of Utah, Salt Lake City, UT 84132-3401, USA; Huntsman Cancer Institute, Salt Lake City, UT, USA.
Christopher GreggDepartment of Neurobiology and Anatomy, University of Utah, Salt Lake City, UT 84132-3401, USA; Department of Human Genetics, University of Utah, Salt Lake City, UT 84132-3401, USA; New York Stem Cell Foundation, New York, NY, USA. Electronic address: chris.gregg@neuro.utah.edu.
University of Utah · USNew York Stem Cell Foundation · US

Funding

UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI KATHARINE S ULLMAN · 1986 to 2026
$72.6M
The Nature and Function of Genomic Imprinting in Monoaminergic NeuronsR01MH109577 · NIMH · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI GREGG, CHRISTOPHER · 2016 to 2025
$5.6M
NCI NIH HHS P30 CA042014NIMH NIH HHS R01 MH109577
6 · The paper itself

Abstract

The identity of most functional elements in the mammalian genome and the phenotypes they impact are unclear. Here, we perform a genome-wide comparative analysis of patterns of accelerated evolution in species with highly distinctive traits to discover candidate functional elements for clinically important phenotypes. We identify accelerated regions (ARs) in the elephant, hibernating bat, orca, dolphin, naked mole rat, and thirteen-lined ground squirrel lineages in mammalian conserved regions, uncovering ∼33,000 elements that bind hundreds of different regulatory proteins in humans and mice. ARs in the elephant, the largest land mammal, are uniquely enriched near elephant DNA damage response genes. The genomic hotspot for elephant ARs is the E3 ligase subunit of the Fanconi anemia complex, a master regulator of DNA repair. Additionally, ARs in the six species are associated with specific human clinical phenotypes that have apparent concordance with overt traits in each species.

Indexed as

Evolution, MolecularQuantitative Trait, HeritableAnimalsConserved SequenceDNA DamageDNA RepairEpigenesis, GeneticFemaleGenetic LociGenomeHumansLymphocytesMammalsMiceMutationNeoplasmsTranscription Factorsaccelerated evolutioncancerelephantenhancerepigeneticsnaked mole ratPeto’s paradoxphylogenomicsregulatory elementsomatic mutation

Identifiers

PMID29514101
PMCPMC6294302
OpenAlexW2789414615

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.