Evidence map›Paper›PMID 37777595›Full record

ArticleScientific reports2023

The blackcap (Sylvia atricapilla) genome reveals a recent accumulation of LTR retrotransposons.

Andrea Bours, Peter Pruisscher, Karen Bascón-Cardozo, Linda Odenthal-Hesse, Miriam Liedvogel

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In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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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

5 authors.

Andrea Bours *MPRG Behavioural Genomics, Max Planck Institute for Evolutionary Biology, 24306, Plön, Germany. bours@evolbio.mpg.de.
Peter Pruisscher *MPRG Behavioural Genomics, Max Planck Institute for Evolutionary Biology, 24306, Plön, Germany.
Karen Bascón-CardozoMPRG Behavioural Genomics, Max Planck Institute for Evolutionary Biology, 24306, Plön, Germany.
Linda Odenthal-HesseDepartment Evolutionary Genetics, Max Planck Institute for Evolutionary Biology, 24306, Plön, Germany.
Miriam LiedvogelMPRG Behavioural Genomics, Max Planck Institute for Evolutionary Biology, 24306, Plön, Germany. liedvogel@evolbio.mpg.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transposable elements (TEs) are mobile genetic elements that can move around the genome, and as such are a source of genomic variability. Based on their characteristics we can annotate TEs within the host genome and classify them into specific TE types and families. The increasing number of available high-quality genome references in recent years provides an excellent resource that will enhance the understanding of the role of recently active TEs on genetic variation and phenotypic evolution. Here we showcase the use of a high-quality TE annotation to understand the distinct effect of recent and ancient TE insertions on the evolution of genomic variation, within our study species the Eurasian blackcap (Sylvia atricapilla). We investigate how these distinct TE categories are distributed along the genome and evaluate how their coverage across the genome is correlated with four genomic features: recombination rate, gene coverage, CpG island coverage and GC content. We found within the recent TE insertions an accumulation of LTRs previously not seen in birds. While the coverage of recent TE insertions was negatively correlated with both GC content and recombination rate, the correlation with recombination rate disappeared and turned positive for GC content when considering ancient TE insertions.

Indexed as

GenomeRetroelementsCpG IslandsDNA Transposable ElementsEvolution, MolecularGenomicsHumansTerminal Repeat SequencesDNA Transposable ElementsRetroelements

Identifiers

PMID37777595
PMCPMC10542752

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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.