Evidence map›Paper›PMID 27440919›Full record

ArticleG3 (Bethesda, Md.)2016

A Genomic Analysis of Factors Driving lincRNA Diversification: Lessons from Plants.

Andrew D L Nelson, Evan S Forsythe, Upendra K Devisetty, David S Clausen, Asher K Haug-Batzell, Ari M R Meldrum, Michael R Frank, Eric Lyons, Mark A Beilstein

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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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

9 authors.

Andrew D L NelsonSchool of Plant Sciences, University of Arizona, Tucson, Arizona 85721 andrewnelson@email.arizona.edu.ORCID 0000-0001-9896-1739
Evan S ForsytheSchool of Plant Sciences, University of Arizona, Tucson, Arizona 85721.
Upendra K DevisettyDepartment of Forest Ecosystems and Society, Oregon State University, Corvalis, Oregon 97331.
David S ClausenDepartment of Statistics, University of Washington, Seattle, Washington 98195.
Asher K Haug-BatzellGenetics Graduate Interdisciplinary Group, University of Arizona, Tucson, Arizona 85721.
Ari M R MeldrumSchool of Plant Sciences, University of Arizona, Tucson, Arizona 85721.
Michael R FrankSchool of Plant Sciences, University of Arizona, Tucson, Arizona 85721.
Eric LyonsSchool of Plant Sciences, University of Arizona, Tucson, Arizona 85721 Genetics Graduate Interdisciplinary Group, University of Arizona, Tucson, Arizona 85721.
Mark A BeilsteinSchool of Plant Sciences, University of Arizona, Tucson, Arizona 85721 andrewnelson@email.arizona.edu.ORCID 0000-0002-3392-1389

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transcriptomic analyses from across eukaryotes indicate that most of the genome is transcribed at some point in the developmental trajectory of an organism. One class of these transcripts is termed long intergenic noncoding RNAs (lincRNAs). Recently, attention has focused on understanding the evolutionary dynamics of lincRNAs, particularly their conservation within genomes. Here, we take a comparative genomic and phylogenetic approach to uncover factors influencing lincRNA emergence and persistence in the plant family Brassicaceae, to which Arabidopsis thaliana belongs. We searched 10 genomes across the family for evidence of > 5000 lincRNA loci from A. thaliana From loci conserved in the genomes of multiple species, we built alignments and inferred phylogeny. We then used gene tree/species tree reconciliation to examine the duplication history and timing of emergence of these loci. Emergence of lincRNA loci appears to be linked to local duplication events, but, surprisingly, not whole genome duplication events (WGD), or transposable elements. Interestingly, WGD events are associated with the loss of loci for species having undergone relatively recent polyploidy. Lastly, we identify 1180 loci of the 6480 previously annotated A. thaliana lincRNAs (18%) with elevated levels of conservation. These conserved lincRNAs show higher expression, and are enriched for stress-responsiveness and cis-regulatory motifs known as conserved noncoding sequences (CNSs). These data highlight potential functional pathways and suggest that CNSs may regulate neighboring genes at both the genomic and transcriptomic level. In sum, we provide insight into processes that may influence lincRNA diversification by providing an evolutionary context for previously annotated lincRNAs.

Indexed as

Evolution, MolecularGenome, PlantPhylogenyArabidopsisBrassicaceaeConserved SequenceGene Expression ProfilingGene Expression Regulation, PlantGenomicsRNA, Long NoncodingRNA, Long NoncodingBrassicaceaecomparative genomicsevolutionlincRNAtranscriptomics

Identifiers

PMID27440919
PMCPMC5015945

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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.