Evidence map›Paper›PMID 14671321›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2003

Homeoprotein DLX-1 interacts with Smad4 and blocks a signaling pathway from activin A in hematopoietic cells.

Shigeru Chiba, Kenichi Takeshita, Yoichi Imai, Keiki Kumano, Mineo Kurokawa, Shigeo Masuda, Kiyoshi Shimizu, Shuji Nakamura, Frank H Ruddle, Hisamaru Hirai

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

26 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Cancers · 2023
    Article
  5. Genome-Wide Association Study forPathogens (Basel, Switzerland) · 2022
    Article
  6. Article
  7. Cancers · 2021
    Review
  8. Massively parallel discovery of human-specific substitutions that alter enhancer activity.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  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

10 authors at 4 institutions in 2 countries.

Shigeru ChibaDepartments of Biology and Human Genetics, Yale University, New Haven, CT 06520-8103, USA. schiba-tky@umin.ac.jp
Kenichi Takeshita
Yoichi Imai
Keiki Kumano
Mineo Kurokawa
Shigeo Masuda
Kiyoshi Shimizu
Shuji Nakamura
Frank H Ruddle
Hisamaru Hirai
The University of Tokyo · JPUniversity Medical Center · USNew York University · USYale University · US

Funding

GENETIC ANALYSIS OF SOMATIC CELL POPULATIONR01GM009966 · NIGMS · YALE UNIVERSITY · PI RUDDLE, FRANK H · 1985 to 2006
$2.2M
GENETIC ANALYSIS OF SOMATIC CELL POPULATIONR37GM009966 · NIGMS · YALE UNIVERSITY · PI RUDDLE, FRANK H · 1990 to 1994
–
NIGMS NIH HHS R01 GM009966NIGMS NIH HHS R37GM09966
6 · The paper itself

Abstract

In the transforming growth factor beta (TGF-beta) superfamily, activin A, TGF-beta1, and bone morphogenic protein 4 (BMP-4) have various effects on hematopoiesis, including early mesodermo-hematogenesis. After these cytokines bind to their respective receptor, a regulatory Smad is phosphorylated and becomes associated with Smad4, the common Smad, and the resulting complex translocates to the nucleus to regulate transcription. DLX1 is the product of a member of the distal-less homeobox gene family, which is known to have important roles in embryogenesis, particularly in craniofacial development, and in GABAergic neurogenesis. DLX1 has been reported to be temporally and spatially coexpressed with BMP-4 during embryogenesis in selected contexts. We report here that, in addition to the previously reported regions/cells, DLX1 is expressed in hematopoietic cells in a lineage-dependent manner and that DLX1 interacts with Smad4 through its homeodomain. We show that it blocks multiple signals from TGF-beta superfamily cytokines such as activin A, TGF-beta1, and BMP-4, including differentiation of a hematopoietic cell line by activin A. Taken together, these data suggest that DLX1 may function as a regulator of multiple signals from TGF-beta superfamily members in broad biological contexts during blood production.

Indexed as

ActivinsDNA-Binding ProteinsDNA, ComplementaryGene LibraryHematopoietic Stem CellsHomeodomain ProteinsHumansInhibin-beta SubunitsLeukemia, Erythroblastic, AcuteMolecular Sequence DataSignal TransductionSmad4 ProteinTrans-ActivatorsTranscription FactorsTumor Cells, Culturedactivin AActivinsDistal-less homeobox proteinsDNA-Binding ProteinsDNA, ComplementaryHomeodomain ProteinsInhibin-beta SubunitsSmad4 ProteinSMAD4 protein, humanTrans-ActivatorsTranscription Factors

Identifiers

PMID14671321
PMCPMC307610
OpenAlexW2016191016

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.