KLF6

Last updated
KLF6
Identifiers
Aliases KLF6 , BCD1, CBA1, COPEB, CPBP, GBF, PAC1, ST12, ZF9, Kruppel-like factor 6, Kruppel like factor 6
External IDs OMIM: 602053; MGI: 1346318; HomoloGene: 996; GeneCards: KLF6; OMA:KLF6 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001008490
NM_001160124
NM_001160125
NM_001300

NM_011803

RefSeq (protein)

NP_001153596
NP_001153597
NP_001291

NP_035933

Location (UCSC) Chr 10: 3.78 – 3.79 Mb Chr 13: 5.91 – 5.92 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Krueppel-like factor 6 is a protein that in humans is encoded by the KLF6 gene. [5]

Contents

It is a tumor suppressor gene. [6]

Function

This gene encodes a nuclear protein that has three zinc fingers at the end of its C-terminal domain, a serine/threonine-rich central region, and an acidic domain lying within the N-terminal region. The zinc fingers of this protein are responsible for the specific DNA binding with the guanine-rich core promoter elements. The central region might be involved in activation or posttranslational regulatory pathways, and the acidic N-terminal domain might play an important role in the process of transcriptional activation. It is capable of activating transcription approximately 4-fold either on homologous or heterologous promoters. The DNA binding and transcriptional activity of this protein, in conjunction with its expression pattern, suggests that this protein may participate in the regulation and/or maintenance of the basal expression of pregnancy-specific glycoprotein genes and possibly other TATA box-less genes. Two transcript variants encoding the same protein have been found for this gene. [7]

Interactions

KLF6 has been shown to interact with Sp1 transcription factor. [8]

See also

Related Research Articles

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<span class="mw-page-title-main">MXD4</span> Protein-coding gene in the species Homo sapiens

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<span class="mw-page-title-main">Scott L. Friedman</span>

Scott L. Friedman is an American scientist, professor and physician who works in the field of hepatology. Friedman has conducted pioneering research into the underlying causes of scarring, or fibrosis, associated with chronic liver disease, by characterizing the key fibrogenic cell type, the hepatic stellate cell His laboratory has also discovered a novel tumor suppressor gene, KLF6 that is inactivated in a number of human cancers including primary liver cancer. Friedman is the Fishberg Professor of Medicine, and Chief of the Division of Liver Diseases, Mount Sinai School of Medicine in New York. Friedman has two children, a son, Leor Friedman, and a daughter, Yael Friedman.

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000067082 Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000000078 Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Onyango P, Koritschoner NP, Patrito LC, Zenke M, Weith A (Feb 1998). "Assignment of the gene encoding the core promoter element binding protein (COPEB) to human chromosome 10p15 by somatic hybrid analysis and fluorescence in situ hybridization". Genomics. 48 (1): 143–4. doi:10.1006/geno.1997.5124. PMID   9503030.
  6. Li D, Yea S, Dolios G, Martignetti JA, Narla G, Wang R, Walsh MJ, Friedman SL (Oct 2005). "Regulation of Kruppel-like factor 6 tumor suppressor activity by acetylation". Cancer Research. 65 (20): 9216–25. doi:10.1158/0008-5472.CAN-05-1040. PMID   16230382.
  7. "Entrez Gene: KLF6 Kruppel-like factor 6".
  8. Botella LM, Sánchez-Elsner T, Sanz-Rodriguez F, Kojima S, Shimada J, Guerrero-Esteo M, Cooreman MP, Ratziu V, Langa C, Vary CP, Ramirez JR, Friedman S, Bernabéu C (Dec 2002). "Transcriptional activation of endoglin and transforming growth factor-beta signaling components by cooperative interaction between Sp1 and KLF6: their potential role in the response to vascular injury". Blood. 100 (12): 4001–10. doi: 10.1182/blood.V100.12.4001 . PMID   12433697.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.