Evidence map›Paper›PMID 31698818›Full record

ArticleGenes2019

Special Issue: Repetitive DNA Sequences.

Sarah E Lower, Anne-Marie Dion-Côté, Andrew G Clark, Daniel A Barbash

Abstract readEditorial
In one paragraph

Article in Genes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
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  11. Review
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.

Sarah E LowerDepartment of Biology, Bucknell University, Lewisburg, PA 17837, USA.
Anne-Marie Dion-CôtéDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14850, USA.
Andrew G ClarkDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14850, USA.
Daniel A BarbashDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14850, USA.

Funding

Heterochromatin and satellite repeat sequence variation in natural populationsR01GM119125 · NIGMS · CORNELL UNIVERSITY · PI BARBASH, DANIEL A, CLARK, ANDREW G · 2017 to 2020
$1.3M
Investigating the evolutionary dynamics and genetic determinants of satellite DNAF32GM126736 · NIGMS · CORNELL UNIVERSITY · PI LOWER, SARAH EMILY · 2017 to 2017
$43k
NIGMS NIH HHS F32 GM126736NIGMS NIH HHS R01 GM119125
6 · The paper itself

Abstract

Repetitive DNAs are ubiquitous in eukaryotic genomes and, in many species, comprise the bulk of the genome. Repeats include transposable elements that can self-mobilize and disperse around the genome and tandemly-repeated satellite DNAs that increase in copy number due to replication slippage and unequal crossing over. Despite their abundance, repetitive DNAs are often ignored in genomic studies due to technical challenges in identifying, assembling, and quantifying them. New technologies and methods are now allowing unprecedented power to analyze repetitive DNAs across diverse taxa. Repetitive DNAs are of particular interest because they can represent distinct modes of genome evolution. Some repetitive DNAs form essential genome structures, such as telomeres and centromeres, that are required for proper chromosome maintenance and segregation, while others form piRNA clusters that regulate transposable elements; thus, these elements are expected to evolve under purifying selection. In contrast, other repeats evolve selfishly and cause genetic conflicts with their host species that drive adaptive evolution of host defense systems. However, the majority of repeats likely accumulate in eukaryotes in the absence of selection due to mechanisms of transposition and unequal crossing over. However, even these "neutral" repeats may indirectly influence genome evolution as they reach high abundance. In this Special Issue, the contributing authors explore these questions from a range of perspectives.

Indexed as

AnimalsCentromereDNA, SatelliteDNA Transposable ElementsEvolution, MolecularGenomeGenomicsHeterochromatinHumansRepetitive Sequences, Nucleic AcidTelomereDNA, SatelliteDNA Transposable ElementsHeterochromatingenome evolutiongenomic conflictheterochromatinrepetitive DNAtransposable element

Identifiers

PMID31698818
PMCPMC6895920

What OpenQuestion holds

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LicenceCC BY
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.