Evidence map›Paper›PMID 14729953›Full record

ArticleMolecular and cellular biology2004

Identification of MoKA, a novel F-box protein that modulates Krüppel-like transcription factor 7 activity.

Silvia Smaldone, Friedrich Laub, Cindy Else, Cecilia Dragomir, Francesco Ramirez

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

29 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Molecular function of Krüppel-like factor 7 in biology.Acta biochimica et biophysica Sinica · 2023
    Review
  7. Article
  8. Article
  9. Krüppel-like Transcription Factor 7 Is a Causal Gene in Autism Development.International journal of molecular sciences · 2022
    Article
  10. FBXO38 Ubiquitin Ligase Controls Centromere Integrity via ZXDA/B Stability.Frontiers in cell and developmental biology · 2022
    Article
  11. FBXO38 Ubiquitin Ligase Controls Sertoli Cell Maturation.Frontiers in cell and developmental biology · 2022
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. The Effect and Mechanism of KLF7 in the TLR4/NF-Mediators of inflammation · 2018
    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

5 authors at 2 institutions in 1 country.

Silvia SmaldoneLaboratory of Genetics and Organogenesis, Hospital for Special Surgery at the Weill Medical College of Cornell University, New York, New York 10021, USA.
Friedrich Laub
Cindy Else
Cecilia Dragomir
Francesco Ramirez
Cornell University · USHospital for Special Surgery · US

Funding

PATHOPHYSIOLOGY OF FIBRILLAR COLLAGEN TYPESR37AR038648 · NIAMS · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI RAMIREZ, FRANCESCO B · 1996 to 2005
$3.0M
PATHOPHYSIOLOGY OF HUMAN FIBRILLAR COLLAGEN TYPESR01AR038648 · NIAMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI RAMIREZ, FRANCESCO B · 1986 to 2011
$1.7M
NIAMS NIH HHS AR38648NIAMS NIH HHS R01 AR038648NIAMS NIH HHS R37 AR038648
6 · The paper itself

Abstract

KLF7, a member of the Krüppel-like transcription factor family, is believed to regulate neurogenesis and cell cycle progression. Here, a yeast two-hybrid screen for KLF7 cofactors in the developing nervous system identified a novel 140-kDa protein named MoKA, for modulator of KLF7 activity. Interaction between MoKA and KLF7 was confirmed by the in vitro glutathione S-transferase pull-down assay and by coimmunoprecipitation of the proteins overexpressed in mammalian cells. Functional assays documented that MoKA is a KLF7 coactivator, and in situ hybridizations identified the developing nervous system and the adult testes as two sites of MoKA and Klf7 coexpression. Chromatin immunoprecipitation experiments demonstrated KLF7 binding to the p21(WAF1/Cip1) gene while transient transfection assays documented KLF7 stimulation of the p21(WAF1/Cip1) proximal promoter. Additional tests revealed that distinct structural motifs of MoKA direct interaction with KLF7 and shuttling between the nucleus and cytoplasm of asynchronously cycling cells. Altogether, our results strongly suggest that MoKA and KLF7 interact functionally to regulate gene expression during cell differentiation and identify the cell cycle regulator p21(WAF1/Cip1) as one of the targeted genes.

Indexed as

Amino Acid SequenceAnimalsCell DifferentiationCyclin-Dependent Kinase Inhibitor p21CyclinsDNA-Binding ProteinsF-Box ProteinsKruppel-Like Transcription FactorsMiceMolecular Sequence DataTranscription FactorsTranscription, GeneticCdkn1a protein, mouseCyclin-Dependent Kinase Inhibitor p21CyclinsDNA-Binding ProteinsF-Box ProteinsFbxo38 protein, mouseKlf7 protein, mouseKruppel-Like Transcription FactorsTranscription Factors

Identifiers

PMID14729953
PMCPMC321422
OpenAlexW2146866576

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.