Evidence map›Paper›PMID 25318671›Full record

ArticleMolecular biology of the cell2014

Neural crest specification and migration independently require NSD3-related lysine methyltransferase activity.

Bridget T Jacques-Fricke, Laura S Gammill

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. NSD2 as a Promising Target in Hematological Disorders.International journal of molecular sciences · 2022
    Review
  7. The role of NSD1, NSD2, and NSD3 histone methyltransferases in solid tumors.Cellular and molecular life sciences : CMLS · 2022
    Review
  8. Specifying neural crest cells: From chromatin to morphogens and factors in between.Wiley interdisciplinary reviews. Developmental biology · 2018
    Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. The small GTPase Arf6 regulates sea urchin morphogenesis.Differentiation; research in biological diversity
    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

2 authors.

Bridget T Jacques-FrickeDepartment of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN 55455.
Laura S GammillDepartment of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN 55455 gammi001@umn.edu.

Funding

A role for the methyltransferase NSD3 in neural crest specification and migrationF32DE021651 · NIDCR · UNIVERSITY OF MINNESOTA · PI JACQUES-FRICKE, BRIDGET T · 2011 to 2013
$163k
NIDCR NIH HHS F32 DE021651
6 · The paper itself

Abstract

Neural crest precursors express genes that cause them to become migratory, multipotent cells, distinguishing them from adjacent stationary neural progenitors in the neurepithelium. Histone methylation spatiotemporally regulates neural crest gene expression; however, the protein methyltransferases active in neural crest precursors are unknown. Moreover, the regulation of methylation during the dynamic process of neural crest migration is unclear. Here we show that the lysine methyltransferase NSD3 is abundantly and specifically expressed in premigratory and migratory neural crest cells. NSD3 expression commences before up-regulation of neural crest genes, and NSD3 is necessary for expression of the neural plate border gene Msx1, as well as the key neural crest transcription factors Sox10, Snail2, Sox9, and FoxD3, but not gene expression generally. Nevertheless, only Sox10 histone H3 lysine 36 dimethylation requires NSD3, revealing unexpected complexity in NSD3-dependent neural crest gene regulation. In addition, by temporally limiting expression of a dominant negative to migratory stages, we identify a novel, direct requirement for NSD3-related methyltransferase activity in neural crest migration. These results identify NSD3 as the first protein methyltransferase essential for neural crest gene expression during specification and show that NSD3-related methyltransferase activity independently regulates migration.

Indexed as

AnimalsAvian ProteinsBody PatterningCatalytic DomainCell MovementChick EmbryoDNA MethylationGene ExpressionGene Expression Regulation, DevelopmentalHistone-Lysine N-MethyltransferaseNeural CrestSnail Family Transcription FactorsSOXE Transcription FactorsTranscription FactorsAvian ProteinsHistone-Lysine N-MethyltransferaseSnail Family Transcription FactorsSOXE Transcription FactorsTranscription Factors

Identifiers

PMID25318671
PMCPMC4263458

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.