Evidence map›Paper›PMID 20573694›Full record

ArticleDevelopment (Cambridge, England)2010

Proliferative and transcriptional identity of distinct classes of neural precursors in the mammalian olfactory epithelium.

Eric S Tucker, Maria K Lehtinen, Tom Maynard, Mariela Zirlinger, Catherine Dulac, Nancy Rawson, Larysa Pevny, Anthony-Samuel Lamantia

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

69 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
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  14. Cell-Cell Communication AlterationsFrontiers in aging neuroscience · 2022
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review

9 more citing papers are in PubMed but not listed here.

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

8 authors at 1 institution in 1 country.

Eric S TuckerDepartment of Cell and Molecular Physiology, University of North Carolina at Chapel Hill, NC 27599, USA.
Maria K Lehtinen
Tom Maynard
Mariela Zirlinger
Catherine Dulac
Nancy Rawson
Larysa Pevny
Anthony-Samuel Lamantia
University of North Carolina at Chapel Hill · US

Funding

Roles of Growth Factor Signaling in Neural RegenerationR01NS031768 · NINDS · WASHINGTON UNIVERSITY · PI SNIDER, WILLIAM D · 1993 to 2016
$6.7M
REGIONAL DIFFERENTIATION DURING FOREBRAIN DEVELOPMENTR01HD029178 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LAMANTIA, ANTHONY S · 1999 to 2010
$3.5M
REGIONAL DIFFERENTIATION DURING FOREBRAIN DEVELOPMENTR29HD029178 · NICHD · DUKE UNIVERSITY · PI LAMANTIA, ANTHONY S · 1993 to 1997
–
NICHD NIH HHS HD029178NICHD NIH HHS R01 HD029178NICHD NIH HHS R29 HD029178NINDS NIH HHS NS031768NINDS NIH HHS R01 NS031768
6 · The paper itself

Abstract

Neural precursors in the developing olfactory epithelium (OE) give rise to three major neuronal classes - olfactory receptor (ORNs), vomeronasal (VRNs) and gonadotropin releasing hormone (GnRH) neurons. Nevertheless, the molecular and proliferative identities of these precursors are largely unknown. We characterized two precursor classes in the olfactory epithelium (OE) shortly after it becomes a distinct tissue at midgestation in the mouse: slowly dividing self-renewing precursors that express Meis1/2 at high levels, and rapidly dividing neurogenic precursors that express high levels of Sox2 and Ascl1. Precursors expressing high levels of Meis genes primarily reside in the lateral OE, whereas precursors expressing high levels of Sox2 and Ascl1 primarily reside in the medial OE. Fgf8 maintains these expression signatures and proliferative identities. Using electroporation in the wild-type embryonic OE in vitro as well as Fgf8, Sox2 and Ascl1 mutant mice in vivo, we found that Sox2 dose and Meis1 - independent of Pbx co-factors - regulate Ascl1 expression and the transition from lateral to medial precursor state. Thus, we have identified proliferative characteristics and a dose-dependent transcriptional network that define distinct OE precursors: medial precursors that are most probably transit amplifying neurogenic progenitors for ORNs, VRNs and GnRH neurons, and lateral precursors that include multi-potent self-renewing OE neural stem cells.

Indexed as

Gene Expression Regulation, DevelopmentalTranscription, GeneticAnimalsCell CycleCell ProliferationElectroporationFemaleImmunohistochemistryMaleMiceMice, TransgenicModels, BiologicalNeuronsOlfactory MucosaStem Cells

Identifiers

PMID20573694
PMCPMC2927697
OpenAlexW2169538657

What OpenQuestion holds

Textmetadata
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.