Evidence map›Paper›PMID 28813670›Full record

ArticleCell reports2017

NKX2-1 Is Required in the Embryonic Septum for Cholinergic System Development, Learning, and Memory.

Lorenza Magno, Caswell Barry, Christoph Schmidt-Hieber, Polyvios Theodotou, Michael Häusser, Nicoletta Kessaris

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
5.1field-weighted citation impact, top 5% 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

46 citing papers in PubMed, 73 citations in OpenAlex.

  1. Article
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  4. DevelopmentalThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
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  8. Sex-specific declines in cholinergic-targeting tRNA fragments in the nucleus accumbens in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2023
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  11. Review
  12. Local Thyroid Hormone Action in Brain Development.International journal of molecular sciences · 2023
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  13. Review
  14. A Human-Specific De Novo Gene Promotes Cortical Expansion and Folding.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
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  15. Article
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  17. Transcription factors in microcephaly.Frontiers in neuroscience · 2023
    Review
  18. Developmental deficits of MGE-derived interneurons in theFrontiers in cell and developmental biology · 2023
    Article
  19. Article
  20. 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

6 authors at 1 institution in 1 country.

Lorenza MagnoWolfson Institute for Biomedical Research, University College London, Gower Street, London WC1E 6BT, UK; Department of Cell and Developmental Biology, University College London, Gower Street, London WC1E 6BT, UK. Electronic address: l.magno@ucl.ac.uk.
Caswell BarryDepartment of Cell and Developmental Biology, University College London, Gower Street, London WC1E 6BT, UK.
Christoph Schmidt-HieberWolfson Institute for Biomedical Research, University College London, Gower Street, London WC1E 6BT, UK; Department of Neuroscience, Physiology and Pharmacology, University College London, Gower Street, London WC1E 6BT, UK.
Polyvios TheodotouWolfson Institute for Biomedical Research, University College London, Gower Street, London WC1E 6BT, UK.
Michael HäusserWolfson Institute for Biomedical Research, University College London, Gower Street, London WC1E 6BT, UK; Department of Neuroscience, Physiology and Pharmacology, University College London, Gower Street, London WC1E 6BT, UK.
Nicoletta KessarisWolfson Institute for Biomedical Research, University College London, Gower Street, London WC1E 6BT, UK; Department of Cell and Developmental Biology, University College London, Gower Street, London WC1E 6BT, UK. Electronic address: n.kessaris@ucl.ac.uk.
University College London · GB

Funding

Biotechnology and Biological Sciences Research Council BB/N009061/1Wellcome Trust 101208/Z/13/ZWellcome Trust 108726/Z/15/ZWellcome Trust 201225/Z/16/Z
6 · The paper itself

Abstract

The transcription factor NKX2-1 is best known for its role in the specification of subsets of cortical, striatal, and pallidal neurons. We demonstrate through genetic fate mapping and intersectional focal septal deletion that NKX2-1 is selectively required in the embryonic septal neuroepithelium for the development of cholinergic septohippocampal projection neurons and large subsets of basal forebrain cholinergic neurons. In the absence of NKX2-1, these neurons fail to develop, causing alterations in hippocampal theta rhythms and severe deficiencies in learning and memory. Our results demonstrate that learning and memory are dependent on NKX2-1 function in the embryonic septum and suggest that cognitive deficiencies that are sometimes associated with pathogenic mutations in NKX2-1 in humans may be a direct consequence of loss of NKX2-1 function.

Indexed as

Gene Expression Regulation, DevelopmentalAcetylcholineAnimalsCholinergic NeuronsCognitionElectrodes, ImplantedEmbryo, MammalianFemaleHippocampusMaleMaze LearningMemoryMiceMice, Inbred C57BLMice, TransgenicRotarod Performance TestAcetylcholineNkx2-1 protein, mouseThyroid Nuclear Factor 1acetylcholinedevelopmenthippocampusseptumtheta

Identifiers

PMID28813670
PMCPMC5565637
OpenAlexW2749159502

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.