Evidence map›Paper›PMID 26538567›Full record

ArticleOpen biology2015

Evolution of lineage-specific functions in ancient cis-regulatory modules.

Stefan Pauls, Debbie K Goode, Libero Petrone, Paola Oliveri, Greg Elgar

Open access · goldAbstract read
In one paragraph

Article in Open biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. Origin and evolution of developmental enhancers in the mammalian neocortex.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
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 3 institutions in 1 country.

Stefan PaulsDivision of Systems Biology, Francis Crick Institute, Mill Hill laboratories, The Ridgeway, Mill Hill, London NW7 1AA, UK.
Debbie K GoodeCambridge Institute for Medical Research and the Wellcome Trust/MRC Cambridge Stem Cell Institute, University of Cambridge, Hills Road, Cambridge CB2 OXY, UK.
Libero PetroneDepartment of Genetics, Evolution and Environment, University College London, Gower Street, London WC1 E6BT, UK.
Paola OliveriDepartment of Genetics, Evolution and Environment, University College London, Gower Street, London WC1 E6BT, UK.
Greg ElgarDivision of Systems Biology, Francis Crick Institute, Mill Hill laboratories, The Ridgeway, Mill Hill, London NW7 1AA, UK greg.elgar@crick.ac.uk.
The Francis Crick Institute · GBUniversity College London · GBUniversity of Cambridge · GB

Funding

Medical Research Council MC_U117597141Medical Research Council U117597141
6 · The paper itself

Abstract

Morphological evolution is driven both by coding sequence variation and by changes in regulatory sequences. However, how cis-regulatory modules (CRMs) evolve to generate entirely novel expression domains is largely unknown. Here, we reconstruct the evolutionary history of a lens enhancer located within a CRM that not only predates the lens, a vertebrate innovation, but bilaterian animals in general. Alignments of orthologous sequences from different deuterostomes sub-divide the CRM into a deeply conserved core and a more divergent flanking region. We demonstrate that all deuterostome flanking regions, including invertebrate sequences, activate gene expression in the zebrafish lens through the same ancient cluster of activator sites. However, levels of gene expression vary between species due to the presence of repressor motifs in flanking region and core. These repressor motifs are responsible for the relatively weak enhancer activity of tetrapod flanking regions. Ray-finned fish, however, have gained two additional lineage-specific activator motifs which in combination with the ancient cluster of activators and the core constitute a potent lens enhancer. The exploitation and modification of existing regulatory potential in flanking regions but not in the highly conserved core might represent a more general model for the emergence of novel regulatory functions in complex CRMs.

Indexed as

Conserved SequenceEvolution, MolecularRegulatory Sequences, Nucleic AcidAnimalsBase SequenceChickensHumansMolecular Sequence DataNucleotide MotifsSOXB2 Transcription FactorsTakifuguXenopusZebrafishSOXB2 Transcription Factorscis-regulatory moduleconserved non-coding elementenhancer evolutionSox21zebrafish

Identifiers

PMID26538567
PMCPMC4680567
OpenAlexW2131158528

What OpenQuestion holds

Textmetadata
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.