Evidence map›Paper›PMID 26475318›Full record

ArticleGenome biology and evolution2015

Early Evolution of Vertebrate Mybs: An Integrative Perspective Combining Synteny, Phylogenetic, and Gene Expression Analyses.

Emeline B Campanini, Michael W Vandewege, Nisha E Pillai, Boon-Hui Tay, Justin L Jones, Byrappa Venkatesh, Federico G Hoffmann

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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed, 23 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

7 authors at 6 institutions in 3 countries.

Emeline B CampaniniDepartament of Genetics and Evolution, Federal University of São Carlos, Brazil.
Michael W VandewegeDepartment of Biochemistry, Molecular Biology, Entomology, and Plant Pathology, Mississippi State University.
Nisha E PillaiInstitute of Molecular and Cell Biology, Comparative and Medical Genomics Laboratory, Agency for Science, Technology and Research, Biopolis, Singapore.
Boon-Hui TayInstitute of Molecular and Cell Biology, Comparative and Medical Genomics Laboratory, Agency for Science, Technology and Research, Biopolis, Singapore.
Justin L JonesDepartment of Biological & Physical Sciences, Saint Augustine's University.
Byrappa VenkateshInstitute of Molecular and Cell Biology, Comparative and Medical Genomics Laboratory, Agency for Science, Technology and Research, Biopolis, Singapore Departments of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore mcbbv@imcb.a-star.edu.sg federico.g.hoffmann@gmail.com.
Federico G HoffmannDepartment of Biochemistry, Molecular Biology, Entomology, and Plant Pathology, Mississippi State University Institute for Genomics, Biocomputing, and Biotechnology, Mississippi State University mcbbv@imcb.a-star.edu.sg federico.g.hoffmann@gmail.com.
Institute of Molecular and Cell Biology · SGAgency for Science, Technology and Research · SGBiocom · USMississippi State University · USSaint Augustine's University · USUniversidade Federal de São Carlos · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The genes in the Myb superfamily encode for three related transcription factors in most vertebrates, A-, B-, and c-Myb, with functionally distinct roles, whereas most invertebrates have a single Myb. B-Myb plays an essential role in cell division and cell cycle progression, c-Myb is involved in hematopoiesis, and A-Myb is involved in spermatogenesis and regulating expression of pachytene PIWI interacting RNAs, a class of small RNAs involved in posttranscriptional gene regulation and the maintenance of reproductive tissues. Comparisons between teleost fish and tetrapods suggest that the emergence and functional divergence of the Myb genes were linked to the two rounds of whole-genome duplication early in vertebrate evolution. We combined phylogenetic, synteny, structural, and gene expression analyses of the Myb paralogs from elephant shark and lampreys with data from 12 bony vertebrates to reconstruct the early evolution of vertebrate Mybs. Phylogenetic and synteny analyses suggest that the elephant shark and Japanese lamprey have copies of the A-, B-, and c-Myb genes, implying their origin could be traced back to the common ancestor of lampreys and gnathostomes. However, structural and gene expression analyses suggest that their functional roles diverged between gnathostomes and cyclostomes. In particular, we did not detect A-Myb expression in testis suggesting that the involvement of A-Myb in the pachytene PIWI interacting RNA pathway is probably a gnathostome-specific innovation. We speculate that the secondary loss of a central domain in lamprey A-Myb underlies the functional differences between the cyclostome and gnathostome A-Myb proteins.

Indexed as

Biological EvolutionPhylogenySyntenyAmino Acid SequenceAnimalsBayes TheoremGenes, mybLampreysLikelihood FunctionsMolecular Sequence DataSequence Analysis, DNASharksVertebratescyclostomegene duplicationgene familygnathostomewhole genome duplication

Identifiers

PMID26475318
PMCPMC5635590
OpenAlexW2177013734

What OpenQuestion holds

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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.