Evidence map›Paper›PMID 24100213›Full record

ArticleMolecular endocrinology (Baltimore, Md.)2013

Cell-specific actions of a human LHX3 gene enhancer during pituitary and spinal cord development.

Soyoung Park, Rachel D Mullen, Simon J Rhodes

Open access · bronzeAbstract read
In one paragraph

Article in Molecular endocrinology (Baltimore, Md.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. A regulatory sequence from theMolecular vision · 2016
    Article
  5. Article
  6. 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

3 authors at 2 institutions in 1 country.

Soyoung ParkPhD, Department of Biology, Indiana University-Purdue University Indianapolis, LD222, 402 North Blackford Street, Indianapolis, IN 46202-5120. srhodes@iupui.edu.
Rachel D Mullen
Simon J Rhodes
Indiana University School of MedicineIndiana University – Purdue University Indianapolis · US

Funding

Role of LHX3 Protein Isoforms in Pituitary DevelopmentR01HD042024 · NICHD · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI RHODES, SIMON JAMES · 2002 to 2012
$2.6M
NICHD NIH HHS HD42024NICHD NIH HHS R01 HD042024
6 · The paper itself

Abstract

The LIM class of homeodomain protein 3 (LHX3) transcription factor is essential for pituitary gland and nervous system development in mammals. In humans, mutations in the LHX3 gene underlie complex pediatric syndromes featuring deficits in anterior pituitary hormones and defects in the nervous system. The mechanisms that control temporal and spatial expression of the LHX3 gene are poorly understood. The proximal promoters of the human LHX3 gene are insufficient to guide expression in vivo and downstream elements including a conserved enhancer region appear to play a role in tissue-specific expression in the pituitary and nervous system. Here we characterized the activity of this downstream enhancer region in regulating gene expression at the cellular level during development. Human LHX3 enhancer-driven Cre reporter transgenic mice were generated to facilitate studies of enhancer actions. The downstream LHX3 enhancer primarily guides gene transcription in α-glycoprotein subunit -expressing cells secreting the TSHβ, LHβ, or FSHβ hormones and expressing the GATA2 and steroidogenic factor 1 transcription factors. In the developing nervous system, the enhancer serves as a targeting module active in V2a interneurons. These results demonstrate that the downstream LHX3 enhancer is important in specific endocrine and neural cell types but also indicate that additional regulatory elements are likely involved in LHX3 gene expression. Furthermore, these studies revealed significant gonadotrope cell heterogeneity during pituitary development, providing insights into the cellular physiology of this key reproductive regulatory cell. The human LHX3 enhancer-driven Cre reporter transgenic mice also provide a valuable tool for further developmental studies of cell determination and differentiation in the pituitary and nervous system.

Indexed as

AnimalsCell LineageCrosses, GeneticEnhancer Elements, GeneticFemaleGATA2 Transcription FactorGenotypeGlycoprotein Hormones, alpha SubunitGonadotrophsGrowth HormoneHumansIntegrasesInterneuronsLIM-Homeodomain ProteinsLuteinizing Hormone, beta SubunitMaleCre recombinaseGATA2 Transcription FactorGlycoprotein Hormones, alpha SubunitGrowth HormoneIntegrasesLhx3 proteinLIM-Homeodomain ProteinsLuteinizing Hormone, beta SubunitTranscription Factors

Identifiers

PMID24100213
PMCPMC3857196
OpenAlexW2081072391

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.