Evidence map›Paper›PMID 27288344›Full record

ArticleMolecular biology and evolution2016

Characterization of Somatically-Eliminated Genes During Development of the Sea Lamprey (Petromyzon marinus).

Stephanie A Bryant, Joseph R Herdy, Chris T Amemiya, Jeramiah J Smith

Open access · bronzeAbstract read
In one paragraph

Article in Molecular biology and evolution, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
12.3field-weighted citation impact, top 2% 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

24 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Article
  3. Biparental inheritance of germline-specific chromosomes in the sea lamprey and their roles in oocytes.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  10. Review
  11. Review
  12. Article
  13. Programmed DNA Elimination in Vertebrates.Annual review of animal biosciences · 2021
    Review
  14. Article
  15. Article
  16. Article
  17. Expansions, diversification, and interindividual copy number variations of AID/APOBEC family cytidine deaminase genes in lampreys.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
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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

4 authors at 1 institution in 1 country.

Stephanie A BryantDepartment of Biology, University of Kentucky.
Joseph R HerdyDepartment of Biology, University of Kentucky.
Chris T AmemiyaBenaroya Research Institute at Virginia Mason, Seattle Department of Biology, University of Washington, Seattle.
Jeramiah J SmithDepartment of Biology, University of Kentucky jjsmit3@uky.edu.
University of Kentucky · US

Funding

Functional analysis of programmed genome rearrangementR01GM104123 · NIGMS · UNIVERSITY OF KENTUCKY · PI SMITH, JERAMIAH JAMES · 2013 to 2017
$1.4M
Germline sequence resources & analyses in a vertebrate model that undergoes PGRR24GM095471 · NIGMS · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI AMEMIYA, CHRIS T. · 2011 to 2014
$1.3M
NIGMS NIH HHS R01 GM104123NIGMS NIH HHS R24 GM095471
6 · The paper itself

Abstract

The sea lamprey (Petromyzon marinus) is a basal vertebrate that undergoes developmentally programmed genome rearrangements (PGRs) during early development. These events facilitate the elimination of ∼20% of the genome from the somatic cell lineage, resulting in distinct somatic and germline genomes. Thus far only a handful of germline-specific genes have been definitively identified within the estimated 500 Mb of DNA that is deleted during PGR, although a few thousand germline-specific genes are thought to exist. To improve our understanding of the evolutionary/developmental logic of PGR, we generated computational predictions to identify candidate germline-specific genes within a new transcriptomic dataset derived from adult germline and the early embryonic stages during which PGR occurs. Follow-up validation studies identified 44 germline-specific genes and further characterized patterns of transcription and DNA loss during early embryogenesis. Expression analyses reveal that many of these genes are differentially expressed during early embryogenesis and presumably function in the early development of the germline. Ontology analyses indicate that many of these germline-specific genes play known roles in germline development, pluripotency, and oncogenesis (when misexpressed). These studies provide support for the theory that PGR serves to segregate molecular functions related to germline development/pluripotency in order to prevent their potential misexpression in somatic cells. This larger set of eliminated genes also allows us to extend the evolutionary/developmental breadth of this theory, as some deleted genes (or their gnathostome homologs) appear to be associated with the early development of somatic lineages, perhaps through the evolution of novel functions within gnathostome lineages.

Indexed as

AnimalsDNAEmbryonic DevelopmentEvolution, MolecularGenomeGerm CellsMalePetromyzonPhylogenySequence Analysis, DNADNAdevelopmentgenomelampreyrearrangementvertebrate.

Identifiers

PMID27288344
PMCPMC4989109
OpenAlexW2415066550

What OpenQuestion holds

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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.