Evidence map›Paper›PMID 22991451›Full record

SynthesisDNA research : an international journal for rapid publication of reports on genes and genomes2012

Identification of novel genes selectively expressed in the follicle-associated epithelium from the meta-analysis of transcriptomics data from multiple mouse cell and tissue populations.

Atsushi Kobayashi, David S Donaldson, Takashi Kanaya, Shinji Fukuda, J Kenneth Baillie, Tom C Freeman, Hiroshi Ohno, Ifor R Williams, Neil A Mabbott

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in DNA research : an international journal for rapid publication of reports on genes and genomes, 2012. 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
0.5field-weighted citation impact, top 34% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Regional heterogeneity in rat Peyer's patches through whole transcriptome analysis.Experimental biology and medicine (Maywood, N.J.) · 2021
    Article
  5. Article
  6. Article
  7. RANK-RANKL Signaling in Cancer of the Uterine Cervix: A Review.International journal of molecular sciences · 2019
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
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

9 authors at 4 institutions in 3 countries.

Atsushi KobayashiThe Roslin Institute and Royal (Dick) School of Veterinary Sciences, University of Edinburgh, Easter Bush, Midlothian EH25 9RG, UK.
David S Donaldson
Takashi Kanaya
Shinji Fukuda
J Kenneth Baillie
Tom C Freeman
Hiroshi Ohno
Ifor R Williams
Neil A Mabbott
RIKEN Center for Integrative Medical Sciences · JPRoslin Institute · GBUniversity of Edinburgh · GBEmory University · US

Funding

Regulation of Organized Intestinal Lymphoid Tissues by TRANCE/RANKLR01DK064730 · NIDDK · EMORY UNIVERSITY · PI WILLIAMS, IFOR R · 2004 to 2012
$2.7M
Biotechnology and Biological Sciences Research Council BB/G003947/1Biotechnology and Biological Sciences Research Council BBS/E/D/05191131Biotechnology and Biological Sciences Research Council BBS/E/D/20211552Biotechnology and Biological Sciences Research Council BBS/E/D/20251967Biotechnology and Biological Sciences Research Council BBS/E/D/20251968NIDDK NIH HHS DK-064730NIDDK NIH HHS R01 DK064730Wellcome Trust
6 · The paper itself

Abstract

The follicle-associated epithelium (FAE) overlying the Peyer's patches and the microfold cells (M cells) within it are important sites of antigen transcytosis across the intestinal epithelium. Using a meta-analysis approach, we identified a transcriptional signature that distinguished the FAE from a large collection of mouse cells and tissues. A co-expressed cluster of 21 FAE-specific genes was identified, and the analysis of the transcription factor binding site motifs in their promoter regions indicated that these genes shared an underlying transcriptional programme. This cluster contained known FAE- (Anxa10, Ccl20, Psg18 and Ubd) and M-cell-specific (Gp2) genes, suggesting that the others were novel FAE-specific genes. Some of these novel candidate genes were expressed highly by the FAE and M cells (Calcb, Ces3b, Clca2 and Gjb2), and others only by the FAE (Ascl2, Cftr, Fgf15, Gpr133, Kcna1, Kcnj15, Mycl1, Pgap1 and Rps6kl). We also identified a subset of novel FAE-related genes that were induced in the intestinal epithelium after receptor activator of nuclear factor (NF)-κB ligand stimulation. These included Mfge8 which was specific to FAE enterocytes. This study provides new insight into the FAE transcriptome. Further characterization of the candidate genes identified here will aid the identification of novel regulators of cell function in the FAE.

Indexed as

TranscriptomeAnimalsAntigens, SurfaceConnexin 26ConnexinsEnterocytesIntestinal MucosaMiceMilk ProteinsNF-kappa BOrgan SpecificityPeyer's PatchesAntigens, SurfaceConnexin 26ConnexinsGJB2 protein, humanMFGE8 protein, humanMilk ProteinsNF-kappa B

Identifiers

PMID22991451
PMCPMC3473373
OpenAlexW2121069469

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.