Evidence map›Paper›PMID 19439491›Full record

ArticleDevelopment (Cambridge, England)2009

Interplay between activin and Hox genes determines the formation of the kidney morphogenetic field.

Ella Preger-Ben Noon, Hila Barak, Noga Guttmann-Raviv, Ram Reshef

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Gene regulatory network of renal primordium development.Pediatric nephrology (Berlin, Germany) · 2014
    Review
  11. Kidney regeneration: common themes from the embryo to the adult.Pediatric nephrology (Berlin, Germany) · 2014
    Review
  12. Review
  13. Article
  14. Article
  15. Analysis of nephric duct specification in the avian embryo.Development (Cambridge, England) · 2012
    Article
  16. Article
  17. Review
  18. Hox genes and kidney development.Pediatric nephrology (Berlin, Germany) · 2011
    Review
  19. Chromatin-based mechanisms of renal epithelial differentiation.Journal of the American Society of Nephrology : JASN · 2011
    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

4 authors at 1 institution in 1 country.

Ella Preger-Ben NoonFaculty of Biology, Technion Israel Institute of Technology, Haifa 32000, Israel.
Hila Barak
Noga Guttmann-Raviv
Ram Reshef
Technion – Israel Institute of Technology · IL

Funding

Patterning the Anterior Border of the Avian PronephrosR03TW006864 · FIC · BETH ISRAEL DEACONESS MEDICAL CENTER · PI SCHULTHEISS, THOMAS M · 2004 to 2006
$102k
FIC NIH HHS 1 R03 TW006864-01
6 · The paper itself

Abstract

The kidney develops in a specific position along the anterior-posterior axis. All vertebrate kidney tissues are derived from the intermediate mesoderm (IM), and early kidney genes such as Lim1 and Pax2 are expressed in amniotes posterior to the sixth somite axial level. IM cells anterior to this level do not express kidney genes owing to changes in their competence to respond to kidney-inductive signals present along the entire axis. We aimed to understand the molecular mechanisms governing the loss of competence of anterior IM cells and the formation of the anterior border of the kidney morphogenetic field. We identified the dorsal neural tube as the potential kidney-inductive tissue and showed that activin, a secreted morphogen, is necessary but insufficient for Lim1 induction and establishment of the kidney field. Activin or activin-like and BMP signaling cascades are activated along the entire axis, including in anterior non-kidney IM, suggesting that competence to respond to these signals involves downstream or other components. Detailed expression pattern analysis of Hox genes during early chick development revealed that paralogous group four genes share the same anterior border as the kidney genes. Ectopic expression of Hoxb4 in anterior non-kidney IM, either by retinoic acid (RA) administration or plasmid-mediated overexpression, resulted in ectopic kidney gene expression. The anterior expansion of Lim1 expression was restrained when Hoxb4 was co-expressed with a truncated form of activin receptor. We suggest a model in which the competence of IM cells to respond to TGFbeta signaling and express kidney genes is driven by RA and mediated by Hoxb4.

Indexed as

ActivinsAnimalsBody PatterningChick EmbryoGene Expression Regulation, DevelopmentalHomeodomain ProteinsKidneyQuailSignal TransductionTransforming Growth Factor betaTretinoinActivinsHomeodomain ProteinsTransforming Growth Factor betaTretinoin

Identifiers

PMID19439491
PMCPMC2685723
OpenAlexW2082460683

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.