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PROX1

From Wikipedia, the free encyclopedia

PROX1
Identifiers
AliasesPROX1, prospero homeobox 1
External IDsOMIM: 601546; MGI: 97772; HomoloGene: 2069; GeneCards: PROX1; OMA:PROX1 - orthologs
Available structures
PDBOrtholog search: PDBe RCSB
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001270616
NM_002763

NM_008937
NM_001360827

RefSeq (protein)

NP_001257545
NP_002754

NP_032963
NP_001347756

Location (UCSC)Chr 1: 213.98 – 214.04 MbChr 1: 189.85 – 189.9 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Prospero homeobox protein 1 is a protein that in humans is encoded by the PROX1 gene.[5][6] The Prox1 gene is critical for the development of multiple tissues. Prox1 activity is necessary and sufficient to specify a lymphatic endothelial cell fate in endothelial progenitors located in the embryonic veins.[7]

Interactions

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PROX1 has been shown to interact with EP300.[8]

Production

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PROX1 is produced primarily in the dentate gyrus in the mouse, and in the dentate gyrus and white matter in humans. Gene expression data for mouse, human and macaque from the Allen Brain Atlases can be found here.

Clinical significance

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PROX1 is used as a marker for lymphatic endothelium in biopsy samples. It has also been identified as an inhibitor of Müller glia (MG)-mediated retinal regeneration in mice that, when blocked from accessing MG cells, allowed retinal regeneration to occur, suggesting a possible therapeutic research pathway for drugs to treat degenerative diseases (such as retinitis pigmentosa) that lead to vision loss.[9]

Homologous gene

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PROX2

References

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  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000117707 Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000010175 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. Zinovieva RD, Duncan MK, Johnson TR, Torres R, Polymeropoulos MH, Tomarev SI (December 1996). "Structure and chromosomal localization of the human homeobox gene Prox 1". Genomics. 35 (3): 517–522. doi:10.1006/geno.1996.0392. PMID 8812486.
  6. "Entrez Gene: PROX1 prospero-related homeobox 1".
  7. Harvey NL, Srinivasan RS, Dillard ME, Johnson NC, Witte MH, Boyd K, et al. (October 2005). "Lymphatic vascular defects promoted by Prox1 haploinsufficiency cause adult-onset obesity". Nature Genetics. 37 (10): 1072–1081. doi:10.1038/ng1642. PMID 16170315. S2CID 25103068.
  8. Chen Q, Dowhan DH, Liang D, Moore DD, Overbeek PA (July 2002). "CREB-binding protein/p300 co-activation of crystallin gene expression". The Journal of Biological Chemistry. 277 (27): 24081–24089. doi:10.1074/jbc.M201821200. PMID 11943779.
  9. Lee EJ, Kim M, Park S, Shim JH, Cho HJ, Park JA, et al. (March 2025). "Restoration of retinal regenerative potential of Müller glia by disrupting intercellular Prox1 transfer". Nature Communications. 16 (1) 2928. Bibcode:2025NatCo..16.2928L. doi:10.1038/s41467-025-58290-8. PMC 11937340. PMID 40133314.

Further reading

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