Evidence map›Paper›PMID 28952437›Full record

ArticleeLife2017

A tissue-specific, Gata6-driven transcriptional program instructs remodeling of the mature arterial tree.

Marta Losa, Victor Latorre, Munazah Andrabi, Franck Ladam, Charles Sagerström, Ana Novoa, Peyman Zarrineh, Laure Bridoux, Neil A Hanley, Moises Mallo and 1 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 34 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

11 authors at 3 institutions in 3 countries.

Marta LosaFaculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
Victor LatorreFaculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
Munazah AndrabiFaculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
Franck LadamDepartment of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, United States.
Charles SagerströmDepartment of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, United States.ORCID http://orcid.org/0000-0002-1509-5810
Ana NovoaInstituto Gulbenkian de Ciência, Oeiras, Portugal.
Peyman ZarrinehFaculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
Laure BridouxFaculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
Neil A HanleyFaculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.ORCID http://orcid.org/0000-0003-3234-4038
Moises MalloInstituto Gulbenkian de Ciência, Oeiras, Portugal.ORCID https://orcid.org/0000-0002-9744-0912
Nicoletta BobolaFaculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.ORCID http://orcid.org/0000-0002-7103-4932
University of Manchester · GBInstituto Gulbenkian de Ciência · PTUniversity of Massachusetts Chan Medical School · US

Funding

MOLECULAR ANALYSIS OF HINDBRAIN FORMATIONR01NS038183 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Charles G Sagerstrom · 1999 to 2026
$8.3M
Molecular Analysis of Hindbrain FormationR56NS038183 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI SAGERSTROM, CHARLES G · 2007 to 2007
$400k
Biotechnology and Biological Sciences Research Council BB/N00907X/1Medical Research Council MR/L009986/1NINDS NIH HHS R01 NS038183NINDS NIH HHS R56 NS038183
6 · The paper itself

Abstract

Connection of the heart to the systemic circulation is a critical developmental event that requires selective preservation of embryonic vessels (aortic arches). However, why some aortic arches regress while others are incorporated into the mature aortic tree remains unclear. By microdissection and deep sequencing in mouse, we find that neural crest (NC) only differentiates into vascular smooth muscle cells (SMCs) around those aortic arches destined for survival and reorganization, and identify the transcription factor Gata6 as a crucial regulator of this process. Gata6 is expressed in SMCs and its target genes activation control SMC differentiation. Furthermore, Gata6 is sufficient to promote SMCs differentiation in vivo, and drive preservation of aortic arches that ought to regress. These findings identify Gata6-directed differentiation of NC to SMCs as an essential mechanism that specifies the aortic tree, and provide a new framework for how mutations in GATA6 lead to congenital heart disorders in humans.

Indexed as

Cell DifferentiationAnimalsAortaGATA6 Transcription FactorGene ExpressionMiceMyocytes, Smooth MuscleNeural CrestGata6 protein, mouseGATA6 Transcription Factordevelopmental biologyembryogreat vesselsmouseneural crestsmooth muscle cellsstem cellstranscription

Identifiers

PMID28952437
PMCPMC5630260
OpenAlexW2759657463

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.