Evidence map›Paper›PMID 26100918›Full record

ArticleDevelopmental biology2015

Molecular asymmetry in the 8-cell stage Xenopus tropicalis embryo described by single blastomere transcript sequencing.

Elena De Domenico, Nick D L Owens, Ian M Grant, Rosa Gomes-Faria, Michael J Gilchrist

Open access · hybridAbstract read
In one paragraph

Article in Developmental biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. RNA localization during early development of the axolotl.Frontiers in cell and developmental biology · 2023
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Transcriptomics and Proteomics Methods forCold Spring Harbor protocols · 2020
    Article
  9. Review
  10. Article
  11. Article
  12. Cap-Independent mRNA Translation in Germ Cells.International journal of molecular sciences · 2019
    Review
  13. Article
  14. Article
  15. Metabolic Comparison of DorsalAnalytical methods : advancing methods and applications · 2017
    Article
  16. Review
  17. Spemann organizer transcriptome induction by early beta-catenin, Wnt, Nodal, and Siamois signals inProceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  18. Article
  19. Review
  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

5 authors at 1 institution in 1 country.

Elena De DomenicoThe Francis Crick Institute, Mill Hill Laboratory, The Ridgeway, Mill Hill, London NW7 1AA, UK.
Nick D L OwensThe Francis Crick Institute, Mill Hill Laboratory, The Ridgeway, Mill Hill, London NW7 1AA, UK.
Ian M GrantThe Francis Crick Institute, Mill Hill Laboratory, The Ridgeway, Mill Hill, London NW7 1AA, UK.
Rosa Gomes-FariaThe Francis Crick Institute, Mill Hill Laboratory, The Ridgeway, Mill Hill, London NW7 1AA, UK.
Michael J GilchristThe Francis Crick Institute, Mill Hill Laboratory, The Ridgeway, Mill Hill, London NW7 1AA, UK. Electronic address: mike.gilchrist@crick.ac.uk.
The Francis Crick Institute · GB

Funding

Medical Research Council A252-5RG70Wellcome Trust
6 · The paper itself

Abstract

Correct development of the vertebrate body plan requires the early definition of two asymmetric, perpendicular axes. The first axis is established during oocyte maturation, and the second is established by symmetry breaking shortly after fertilization. The physical processes generating the second asymmetric, or dorsal-ventral, axis are well understood, but the specific molecular determinants, presumed to be maternal gene products, are poorly characterized. Whilst enrichment of maternal mRNAs at the animal and vegetal poles in both the oocyte and the early embryo has been studied, little is known about the distribution of maternal mRNAs along either the dorsal-ventral or left-right axes during the early cleavage stages. Here we report an unbiased analysis of the distribution of maternal mRNA on all axes of the Xenopus tropicalis 8-cell stage embryo, based on sequencing of single blastomeres whose positions within the embryo are known. Analysis of pooled data from complete sets of blastomeres from four embryos has identified 908 mRNAs enriched in either the animal or vegetal blastomeres, of which 793 are not previously reported as enriched. In contrast, we find no evidence for asymmetric distribution along either the dorsal-ventral or left-right axes. We confirm that animal pole enrichment is on average distinctly lower than vegetal pole enrichment, and that considerable variation is found between reported enrichment levels in different studies. We use publicly available data to show that there is a significant association between genes with human disease annotation and enrichment at the animal pole. Mutations in the human ortholog of the most animally enriched novel gene, Slc35d1, are causative for Schneckenbecken dysplasia, and we show that a similar phenotype is produced by depletion of the orthologous protein in Xenopus embryos.

Indexed as

AnimalsBlastomeresBody PatterningFemaleGene Knockdown TechniquesHumansMaleModels, AnimalMonosaccharide Transport ProteinsMutationRNA, MessengerTranscription, GeneticXenopusXenopus ProteinsMonosaccharide Transport ProteinsRNA, MessengerSLC35D1 protein, humanXenopus ProteinsCortical rotationDorsal determinantsMolecular asymmetryPolar enrichment of mRNAsSpatial distribution of maternal mRNAsXenopus tropicalis

Identifiers

PMID26100918
PMCPMC4684228
OpenAlexW635876790

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.