Evidence map›Paper›PMID 21876128›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2011

Convergent evolution of two mammalian neuronal enhancers by sequential exaptation of unrelated retroposons.

Lucía F Franchini, Rodrigo López-Leal, Sofía Nasif, Paula Beati, Diego M Gelman, Malcolm J Low, Flávio J S de Souza, Marcelo Rubinstein

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
7.4field-weighted citation impact, top 3% 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

52 citing papers in PubMed, 83 citations in OpenAlex.

  1. Article
  2. Article
  3. A mammalian tripartite enhancer cluster controls hypothalamicProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
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  10. Article
  11. Article
  12. Review
  13. Article
  14. Enhancer redundancy in development and disease.Nature reviews. Genetics · 2021
    Review
  15. Review
  16. Article
  17. Transposable Elements and Stress in Vertebrates: An Overview.International journal of molecular sciences · 2021
    Review
  18. Review
  19. Genetic Mechanisms Underlying Cortical Evolution in Mammals.Frontiers in cell and developmental biology · 2021
    Review
  20. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

8 authors at 5 institutions in 3 countries.

Lucía F FranchiniInstituto de Investigaciones en Ingeniería Genética y Biología Molecular, Consejo Nacional de Investigaciones Científicas y Técnicas, C1428ADN Buenos Aires, Argentina.
Rodrigo López-Leal
Sofía Nasif
Paula Beati
Diego M Gelman
Malcolm J Low
Flávio J S de Souza
Marcelo Rubinstein
Consejo Nacional de Investigaciones Científicas y Técnicas · ARCentro de Estudios Científicos · CLExperimental Medicine and Biology Institute · ARFundación Ciencias Exactas y Naturales · ARUniversity of Michigan–Ann Arbor · US

Funding

Proopiomelanocortin Gene Expression and ObesityR01DK068400 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LOW, MALCOLM JAMES · 2004 to 2022
$6.6M
Howard Hughes Medical InstituteNIDDK NIH HHS DK068400NIDDK NIH HHS R01 DK068400
6 · The paper itself

Abstract

The proopiomelanocortin gene (POMC) is expressed in a group of neurons present in the arcuate nucleus of the hypothalamus. Neuron-specific POMC expression in mammals is conveyed by two distal enhancers, named nPE1 and nPE2. Previous transgenic mouse studies showed that nPE1 and nPE2 independently drive reporter gene expression to POMC neurons. Here, we investigated the evolutionary mechanisms that shaped not one but two neuron-specific POMC enhancers and tested whether nPE1 and nPE2 drive identical or complementary spatiotemporal expression patterns. Sequence comparison among representative genomes of most vertebrate classes and mammalian orders showed that nPE1 is a placental novelty. Using in silico paleogenomics we found that nPE1 originated from the exaptation of a mammalian-apparent LTR retrotransposon sometime between the metatherian/eutherian split (147 Mya) and the placental mammal radiation (≈ 90 Mya). Thus, the evolutionary origin of nPE1 differs, in kind and time, from that previously demonstrated for nPE2, which was exapted from a CORE-short interspersed nucleotide element (SINE) retroposon before the origin of prototherians, 166 Mya. Transgenic mice expressing the fluorescent markers tomato and EGFP driven by nPE1 or nPE2, respectively, demonstrated coexpression of both reporter genes along the entire arcuate nucleus. The onset of reporter gene expression guided by nPE1 and nPE2 was also identical and coincidental with the onset of Pomc expression in the presumptive mouse diencephalon. Thus, the independent exaptation of two unrelated retroposons into functional analogs regulating neuronal POMC expression constitutes an authentic example of convergent molecular evolution of cell-specific enhancers.

Indexed as

Evolution, MolecularAnimalsBase SequenceEnhancer Elements, GeneticFemaleGene Expression Regulation, DevelopmentalGenes, ReporterHumansMammalsMiceMice, TransgenicMolecular Sequence DataNeuronsPhylogenyPlacentaPregnancyPro-OpiomelanocortinRetroelements

Identifiers

PMID21876128
PMCPMC3174587
OpenAlexW2028548770

What OpenQuestion holds

Textmetadata
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.