Evidence map›Paper›PMID 25618141›Full record

ArticleGenome biology and evolution2015

Highly constrained intergenic Drosophila ultraconserved elements are candidate ncRNAs.

Andrew D Kern, Daniel A Barbash, Joshua Chang Mell, Daniel Hupalo, Amanda Jensen

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

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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

5 authors at 4 institutions in 2 countries.

Andrew D KernDepartment of Genetics, Rutgers University kern@biology.rutgers.edu.
Daniel A BarbashDepartment of Molecular Biology and Genetics, Cornell University.
Joshua Chang MellDepartment of Microbiology and Immunology, Drexel University College of Medicine.
Daniel HupaloDepartment of Biology, Dartmouth College, Hanover, New Hampshire.
Amanda JensenDepartment of Biology, Dartmouth College, Hanover, New Hampshire.
Dartmouth College · USDrexel University · USPediatrics and Genetics · USRutgers Sexual and Reproductive Health and Rights · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eukaryotes contain short (∼80-200 bp) regions that have few or no substitutions among species that represent hundreds of millions of years of evolutionary divergence. These ultraconserved elements (UCEs) are candidates for containing essential functions, but their biological roles remain largely unknown. Here, we report the discovery and characterization of UCEs from 12 sequenced Drosophila species. We identified 98 elements ≥80 bp long with very high conservation across the Drosophila phylogeny. Population genetic analyses reveal that these UCEs are not present in mutational cold spots. Instead we infer that they experience a level of selective constraint almost 10-fold higher compared with missense mutations in protein-coding sequences, which is substantially higher than that observed previously for human UCEs. About one-half of these Drosophila UCEs overlap the transcribed portion of genes, with many of those that are within coding sequences likely to correspond to sites of ADAR-dependent RNA editing. For the remaining UCEs that are in nongenic regions, we find that many are potentially capable of forming RNA secondary structures. Among ten chosen for further analysis, we discovered that the majority are transcribed in multiple tissues of Drosophila melanogaster. We conclude that Drosophila species are rich with UCEs and that many of them may correspond to novel noncoding RNAs.

Indexed as

AnimalsBase SequenceConserved SequenceDrosophila melanogasterGenomicsMolecular Sequence AnnotationRNA, UntranslatedSelection, GeneticRNA, Untranslatedcomparative genomicsnatural selectionncRNAsultraconserved elements

Identifiers

PMID25618141
PMCPMC5322558
OpenAlexW2151710573

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.