Evidence map›Paper›PMID 27230062›Full record

ArticleBMC evolutionary biology2016

A pancreatic exocrine-like cell regulatory circuit operating in the upper stomach of the sea urchin Strongylocentrotus purpuratus larva.

Margherita Perillo, Yue Julia Wang, Steven D Leach, Maria Ina Arnone

Open access · goldAbstract read
In one paragraph

Article in BMC evolutionary biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 38 citations in OpenAlex.

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  14. Gastrulation in the sea urchin.Current topics in developmental biology · 2020
    Review
  15. Transcription factor Ptf1a in development, diseases and reprogramming.Cellular and molecular life sciences : CMLS · 2019
    Review
  16. Article
  17. 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

4 authors at 3 institutions in 2 countries.

Margherita PerilloBiology and Evolution of Marine Organisms, Stazione Zoologica Anton Dohrn, Napoli, 80121, Italy.
Yue Julia WangDepartment of Surgery and the McKusick Nathans Institute for Genetic Medicine, Johns Hopkins University, Baltimore, MD, 21205, USA.
Steven D LeachDepartment of Surgery and the McKusick Nathans Institute for Genetic Medicine, Johns Hopkins University, Baltimore, MD, 21205, USA.
Maria Ina ArnoneBiology and Evolution of Marine Organisms, Stazione Zoologica Anton Dohrn, Napoli, 80121, Italy. miarnone@szn.it.
Johns Hopkins University · USBoston College · USStazione Zoologica Anton Dohrn · IT

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Regulation of Exocrine Pancreatic Progenitors by Ptf1a-p48R01DK061215 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI LEACH, STEVEN D · 2002 to 2012
$3.3M
NCI NIH HHS P30 CA008748NIDDK NIH HHS R01 DK061215
6 · The paper itself

Abstract

backgroundDigestive cells are present in all metazoans and provide the energy necessary for the whole organism. Pancreatic exocrine cells are a unique vertebrate cell type involved in extracellular digestion of a wide range of nutrients. Although the organization and regulation of this cell type is intensively studied in vertebrates, its evolutionary history is still unknown. In order to understand which are the elements that define the pancreatic exocrine phenotype, we have analyzed the expression of genes that contribute to specification and function of this cell-type in an early branching deuterostome, the sea urchin Strongylocentrotus purpuratus.

resultsWe defined the spatial and temporal expression of sea urchin orthologs of pancreatic exocrine genes and described a unique population of cells clustered in the upper stomach of the sea urchin embryo where exocrine markers are co-expressed. We used a combination of perturbation analysis, drug and feeding experiments and found that in these cells of the sea urchin embryo gene expression and gene regulatory interactions resemble that of bona fide pancreatic exocrine cells. We show that the sea urchin Ptf1a, a key transcriptional activator of digestive enzymes in pancreatic exocrine cells, can substitute for its vertebrate ortholog in activating downstream genes.

conclusionsCollectively, our study is the first to show with molecular tools that defining features of a vertebrate cell-type, the pancreatic exocrine cell, are shared by a non-vertebrate deuterostome. Our results indicate that the functional cell-type unit of the vertebrate pancreas may evolutionarily predate the emergence of the pancreas as a discrete organ. From an evolutionary perspective, these results encourage to further explore the homologs of other vertebrate cell-types in traditional or newly emerging deuterostome systems.

Indexed as

Biological EvolutionAnimalsCell DifferentiationCell LineageDigestionGene Expression Regulation, DevelopmentalGenes, RegulatorHEK293 CellsHeLa CellsHumansLarvaPancreasRatsStomachStrongylocentrotus purpuratusTranscription Factorstranscription factor PTF1Transcription FactorsAmylaseCarboxypeptidasePancreasPancreatic lipasePtf1aStrogylocentrotus purpuratus

Identifiers

PMID27230062
PMCPMC4880809
OpenAlexW2407177858

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.