PRRX1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Paired related homeobox 1 is a protein that in humans is encoded by the PRRX1 gene.[5][6]

AliasesPRRX1, AGOTC, PHOX1, PMX1, PRX-1, PRX1, paired related homeobox 1
End170,739,421 bp[1]
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PRRX1
Identifiers
AliasesPRRX1, AGOTC, PHOX1, PMX1, PRX-1, PRX1, paired related homeobox 1
External IDsOMIM: 167420; MGI: 97712; HomoloGene: 7896; GeneCards: PRRX1; OMA:PRRX1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_006902
NM_022716

NM_001025570
NM_011127
NM_175686

RefSeq (protein)

NP_008833
NP_073207

NP_001020741
NP_035257
NP_783617

Location (UCSC)Chr 1: 170.66 – 170.74 MbChr 1: 163.07 – 163.14 Mb
PubMed search[3][4]
Wikidata
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Function

The DNA-associated protein encoded by this gene is a member of the paired family of homeobox proteins localized to the nucleus. The protein functions as a transcription coactivator, enhancing the DNA-binding activity of serum response factor, a protein required for the induction of genes by growth and differentiation factors. The protein regulates muscle creatine kinase, indicating a role in the establishment of diverse mesodermal muscle types. Alternative splicing yields two isoforms that differ in abundance and expression patterns.[6]

Role in mesenchymal stem cell differentiation

Prrx1 expression is restricted to the mesoderm during embryonic development, and both Prrx1 and Prrx2 are expressed in mesenchymal tissues in adult mice.[7][8][9][10][11] Mice that lack both Prrx1 and Prrx2 have profound defects in mesenchymal cell differentiation in the craniofacial region.[9][12] Several recent studies demonstrate that PRRX1 can regulate differentiation of mesenchymal precursors. For example, PRRX1 inhibits adipogenesis by activating transforming growth factor-beta (TGF-beta) signaling,[13] and also acts downstream of tumor necrosis factor-alpha to inhibit osteoblast differentiation.[14]

References

Further reading

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