Evidence map›Paper›PMID 21384471›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2011

HMGB factors are required for posterior digit development through integrating signaling pathway activities.

Junji Itou, Noboru Taniguchi, Isao Oishi, Hiroko Kawakami, Martin Lotz, Yasuhiko Kawakami

Open access · bronzeAbstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2011. 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
1.5field-weighted citation impact, top 19% 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, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Characterization of the Zebrafish Cell Landscape at Single-Cell Resolution.Frontiers in cell and developmental biology · 2021
    Article
  9. Review
  10. Review
  11. Article
  12. Small non-coding RNA and colorectal cancer.Journal of cellular and molecular medicine · 2019
    Review
  13. Article
  14. Regulatory miRNAs in Colorectal Carcinogenesis and Metastasis.International journal of molecular sciences · 2017
    Review
  15. Review
  16. Article
  17. Article
  18. HMGB1 in health and disease.Molecular aspects of medicine · 2014
    Review
  19. Article
  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

6 authors at 3 institutions in 2 countries.

Junji ItouDepartment of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, Minnesota, USA.
Noboru Taniguchi
Isao Oishi
Hiroko Kawakami
Martin Lotz
Yasuhiko Kawakami
University of Minnesota · USScripps Research Institute · USZero to Three · US

Funding

TISSUE ACQUISITION, MORPHOLOGY, AND CELL CULTUREP01AG007996 · NIA · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI SAH, ROBERT L · 1989 to 2016
$26.0M
HMGB2 in cartilage homeostasis, aging and osteoarthritisR01AR056026 · NIAMS · SCRIPPS RESEARCH INSTITUTE, THE · PI LOTZ, MARTIN K · 2009 to 2013
$2.0M
NIAMS NIH HHS AR056026NIAMS NIH HHS R01 AR056026NIA NIH HHS AG007996NIA NIH HHS P01 AG007996
6 · The paper itself

Abstract

The chromatin factors Hmgb1 and Hmgb2 have critical roles in cellular processes, including transcription and DNA modification. To identify the function of Hmgb genes in embryonic development, we generated double mutants of Hmgb1;Hmgb2 in mice. While double null embryos arrest at E9.5, Hmgb1(-/-) ; Hmgb2(+/-) embryos exhibit a loss of digit5, the most posterior digit, in the forelimb. We show that Hmgb1(-/-) ; Hmgb2(+/-) forelimbs have a reduced level of Shh signaling, as well as a clear downregulation of Wnt and BMP target genes in the posterior region. Moreover, we demonstrate that hmgb1 and hmgb2 in zebrafish embryos enhance Wnt signaling in a variety of tissues, and that double knockdown embryos have reduced Wnt signaling and shh expression in pectoral fin buds. Our data show that Hmgb1 and Hmgb2 function redundantly to enhance Wnt signaling in embryos, and further suggest that integrating Wnt, Shh, and BMP signaling regulates the development of digit5 in forelimbs.

Indexed as

AnimalsBone Morphogenetic ProteinsEmbryo, MammalianExtremitiesFemaleGene Expression Regulation, DevelopmentalHedgehog ProteinsHMGB1 ProteinHMGB2 ProteinHMGB ProteinsImmunohistochemistryIn Situ HybridizationMiceMice, Mutant StrainsModels, BiologicalPregnancyBone Morphogenetic ProteinsHedgehog ProteinsHMGB1 ProteinHMGB2 ProteinHMGB ProteinsShh protein, mouseWnt Proteins

Identifiers

PMID21384471
PMCPMC3081368
OpenAlexW2047568249

What OpenQuestion holds

Textmetadata
LicenceTDM
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.