Evidence map›Paper›PMID 21138943›Full record

ArticleHuman molecular genetics2011

Esrrg functions in early branch generation of the ureteric bud and is essential for normal development of the renal papilla.

Rachel Berry, Louise Harewood, Liming Pei, Malcolm Fisher, David Brownstein, Allyson Ross, William A Alaynick, Julie Moss, Nicholas D Hastie, Peter Hohenstein and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Human molecular genetics, 2011. 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
0.9field-weighted citation impact, top 26% 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, 35 citations in OpenAlex.

  1. Review
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  7. Genomic integration of ERRγ-HNF1β regulates renal bioenergetics and prevents chronic kidney disease.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  8. Article
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  12. Article
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  14. Review
  15. Article
  16. Article
  17. Article
  18. Angiotensin II regulates growth of the developing papillas ex vivo.American journal of physiology. Renal physiology · 2012
    Article
  19. Article
  20. Wnt signaling and renal medulla formation.Pediatric nephrology (Berlin, Germany) · 2011
    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

13 authors at 5 institutions in 2 countries.

Rachel BerryMRC Human Genetics Unit, Institute of Genetic and Molecular Medicine, Western General Hospital, Edinburgh EH4 2XU, UK.
Louise Harewood
Liming Pei
Malcolm Fisher
David Brownstein
Allyson Ross
William A Alaynick
Julie Moss
Nicholas D Hastie
Peter Hohenstein
Jamie A Davies
Ronald M Evans
David R FitzPatrick
MRC Institute of Genetics and Molecular Medicine · GBHoward Hughes Medical Institute · USUniversity of Edinburgh · GBWestern General Hospital · GBSalk Institute for Biological Studies · US

Funding

Viral Vector Core (VVC)P30CA014195 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Ye Zheng · 1985 to 2026
$82.8M
HORMONAL REGULATION OF MAMMALIAN GENE EXPRESSIONR37DK057978 · NIDDK · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI EVANS, RONALD M · 2000 to 2019
$16.0M
Spatial Regulation of Developmental Gene ExpressionR01HL105278 · NHLBI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI EVANS, RONALD M · 2011 to 2019
$4.0M
Biotechnology and Biological Sciences Research Council G19227Howard Hughes Medical InstituteMedical Research Council MC_U127527180
6 · The paper itself

Abstract

Congenital anomalies of the kidney and urinary tract (CAKUTs) are common disorders of human development affecting the renal parechyma, renal pelvis, ureter, bladder and urethra; they show evidence of shared genetic aetiology, although the molecular basis of this remains unknown in the majority of cases. Breakpoint mapping of a de novo, apparently balanced, reciprocal translocation associated with bilateral renal agenesis has implicated the gene encoding the nuclear steroid hormone receptor ESRRG as a candidate gene for CAKUT. Here we show that the Esrrg protein is detected throughout early ureteric ducts as cytoplasmic/sub-membranous staining; with nuclear localization seen in developing nephrons. In 14.5-16.5 dpc (days post-conception) mouse embryos, Esrrg localizes to the subset of ductal tissue within the kidney, liver and lung. The renal ductal expression becomes localized to renal papilla by 18.5 dpc. Perturbation of function was performed in embryonic mouse kidney culture using pooled siRNA to induce knock-down and a specific small-molecule agonist to induce aberrant activation of Esrrg. Both resulted in severe abnormality of early branching events of the ureteric duct. Mouse embryos with a targeted inactivation of Esrrg on both alleles (Esrrg(-/-)) showed agenesis of the renal papilla but normal development of the cortex and remaining medulla. Taken together, these results suggest that Esrrg is required for early branching events of the ureteric duct that occur prior to the onset of nephrogenesis. These findings confirm ESRRG as a strong candidate gene for CAKUT.

Indexed as

AnimalsCongenital AbnormalitiesGene Expression Regulation, DevelopmentalHumansKidneyKidney DiseasesKidney MedullaMiceMice, KnockoutOrganogenesisReceptors, EstrogenUreterEsrrg protein, mouseReceptors, Estrogen

Identifiers

PMID21138943
PMCPMC3033182
OpenAlexW2116319684

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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.