Evidence map›Paper›PMID 28516231›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society2017

Molecular evolution of type II MAGE genes from ancestral MAGED2 gene and their phylogenetic resolution of basal mammalian clades.

Marcos De Donato, Sunday O Peters, Tanveer Hussain, Hectorina Rodulfo, Bolaji N Thomas, Masroor E Babar, Ikhide G Imumorin

Abstract read
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In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Evolutionary and Expression Analysis of the Pig MAGE Gene Family.Animals : an open access journal from MDPI · 2024
    Article
  5. Article
  6. Article
  7. Pathogenicity of the MAGE family.Oncology letters · 2021
    Review
  8. Necdin: A purposive integrator of molecular interaction networks for mammalian neuron vitality.Genes to cells : devoted to molecular & cellular mechanisms · 2021
    Review
  9. Review
  10. Article
  11. Article
  12. Sequence variation of necdin gene in Bovidae.Journal of animal science and technology · 2018
    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

7 authors at 6 institutions in 3 countries.

Marcos De DonatoAnimal Genetics and Genomics Laboratory, International Programs, College of Agriculture and Life Science, Cornell University, Ithaca, NY, 14853, USA.ORCID http://orcid.org/0000-0001-8860-6020
Sunday O PetersDepartment of Animal Science, Berry College, Mount Berry, GA, 30149, USA.
Tanveer HussainAnimal Genetics and Genomics Laboratory, International Programs, College of Agriculture and Life Science, Cornell University, Ithaca, NY, 14853, USA.
Hectorina RodulfoEscuela de Escuela de Bioingenierias, Instituto Tecnologico y de Estudios Superiores de Monterrey, Queretaro, Mexico.
Bolaji N ThomasDepartment of Biomedical Sciences, Rochester Institute of Technology, Rochester, NY, 14623, USA.
Masroor E BabarDepartment of Molecular Biology, Virtual University of Pakistan, Lahore, 54000, Pakistan.
Ikhide G ImumorinAnimal Genetics and Genomics Laboratory, International Programs, College of Agriculture and Life Science, Cornell University, Ithaca, NY, 14853, USA. igi2@cornell.edu.
Cornell University · USBerry College · USGeorgia Institute of Technology · USRochester Institute of Technology · USTecnológico de Monterrey · MXVirtual University of Pakistan · PK

Funding

National Research Initiative Competitive Grant Program 2006-35205-16864USDA National Institute of Food and Agriculture 2009-65205-05635USDA-NIFA Research Agreements 2010-34444-20729
6 · The paper itself

Abstract

Type II melanoma-associated antigens (MAGE) are a subgroup of about a dozen proteins found in various locations in the genome and expressed in normal tissues, thus are not related to cancer as the type I MAGE genes. This gene family exists as a single copy in non-mammals and monotremata, but found as two copies in metatherians and occur as a diverse group in all eutherians. Our studies suggest MAGED2 as the ancestor of this subfamily and the most likely evolutionary history of eutherian type II MAGE genes is hereby proposed based on synteny conservation, phylogenetic relations, genome location, homology conservation, and the protein and gene structures. Type II genes can be divided into two: those with 13 exons (MAGED1, MAGED2, TRO, and MAGED4) and those with only one exon (MAGEE1, MAGEE2, MAGEF1, NSMCE3, MAGEH1, MAGEL2, and NDN) with different evolutionary patterns. Our results suggest a need to change the gene nomenclature to MAGE1 (the ancestral gene), currently designated as LOC103095671 and LOC100935086, in opossum and Tasmanian devil, respectively, and MAGE2 (the duplicated one), currently designated as LOC100617402 and NDNL2, respectively, to avoid confusion. We reconstructed the phylogenetic relationships among 23 mammalian species using the combined sequences of MAGED1, MAGED2, MAGEL2, and NDN, because of their high divergence, and found high levels of support, being able to resolve the phylogenetic relationships among Euarchontoglires, Laurasiatheria, Afrotheria, and Xenarthra, as an example that small, but phylogenetically informative sequences, can be very useful for resolving basal mammalian clades.

Indexed as

Evolution, MolecularPhylogenyAnimalsAntigens, NeoplasmEutheriaExonsGene DuplicationGenetic MarkersGenomeMammalsMelanoma-Specific AntigensSequence Analysis, DNASequence Analysis, ProteinSyntenyAntigens, NeoplasmGenetic MarkersMelanoma-Specific AntigensAncestral GeneDuplication EventEutherian EvolutionRapid DiversificationTasmanian Devil

Identifiers

PMID28516231
OpenAlexW2614111990

What OpenQuestion holds

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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.