Pituitary-specific positive transcription factor 1

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POU class 1 homeobox 1

PDB rendering based on 1au7.
Available structures
PDB Ortholog search: PDBe, RCSB
Identifiers
Symbols POU1F1 ; CPHD1; GHF-1; PIT1; POU1F1a; Pit-1
External IDs OMIM173110 MGI97588 HomoloGene259 GeneCards: POU1F1 Gene
RNA expression pattern
PBB GE POU1F1 207846 at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez 5449 18736
Ensembl ENSG00000064835 ENSMUSG00000004842
UniProt P28069 Q00286
RefSeq (mRNA) NM_000306 NM_008849
RefSeq (protein) NP_000297 NP_032875
Location (UCSC) Chr 3:
87.31 – 87.33 Mb
Chr 16:
65.52 – 65.54 Mb
PubMed search [1] [2]

POU domain, class 1, transcription factor 1 (Pit1, growth hormone factor 1), also known as POU1F1, is a transcription factor for growth hormone.[1]

PIT1 is a pituitary-specific transcription factor responsible for pituitary development and hormone expression in mammals and is a member of the POU family of transcription factors that regulate mammalian development. The POU family is so named because the first 3 members identified were PIT1 and OCT1 (MIM 164175) of mammals, and Unc-86 of C. elegans (Herr et al., 1988). PIT1 contains 2 protein domains, termed POU-specific and POU-homeo, which are both necessary for high affinity DNA binding on genes encoding growth hormone (GH; MIM 139250) and prolactin (PRL; MIM 176760). PIT1 is also important for regulation of the genes encoding prolactin and thyroid-stimulating hormone beta subunit (TSHB; MIM 188540) by thyrotropin-releasing hormone (TRH; MIM 257120) and cyclic AMP.[supplied by OMIM][1]

Interactions[edit]

Pituitary-specific positive transcription factor 1 has been shown to interact with GATA2[2] and PITX1.[3]

References[edit]

  1. ^ a b "Entrez Gene: POU1F1 POU domain, class 1, transcription factor 1 (Pit1, growth hormone factor 1)". 
  2. ^ Dasen, J S; O'Connell S M, Flynn S E, Treier M, Gleiberman A S, Szeto D P, Hooshmand F, Aggarwal A K, Rosenfeld M G (May 1999). "Reciprocal interactions of Pit1 and GATA2 mediate signaling gradient-induced determination of pituitary cell types". Cell (UNITED STATES) 97 (5): 587–98. doi:10.1016/S0092-8674(00)80770-9. ISSN 0092-8674. PMID 10367888. 
  3. ^ Szeto, D P; Ryan A K, O'Connell S M, Rosenfeld M G (July 1996). "P-OTX: a PIT-1-interacting homeodomain factor expressed during anterior pituitary gland development". Proc. Natl. Acad. Sci. U.S.A. (UNITED STATES) 93 (15): 7706–10. doi:10.1073/pnas.93.15.7706. ISSN 0027-8424. PMC 38811. PMID 8755540. 

Further reading[edit]

  • Parks JS, Brown MR (1999). "Transcription factors regulating pituitary development". Growth Horm. IGF Res. 9 Suppl B: 2–8; discussion 8–11. doi:10.1016/S1096-6374(99)80074-4. PMID 10549299. 
  • Rodriguez R, Andersen B (2003). "Cellular determination in the anterior pituitary gland: PIT-1 and PROP-1 mutations as causes of human combined pituitary hormone deficiency". Minerva Endocrinol. 28 (2): 123–33. PMID 12717343. 
  • Quentien MH, Barlier A, Franc JL et al. (2006). "Pituitary transcription factors: from congenital deficiencies to gene therapy". J. Neuroendocrinol. 18 (9): 633–42. doi:10.1111/j.1365-2826.2006.01461.x. PMID 16879162. 
  • Cattini PA, Yang X, Jin Y, Detillieux KA (2006). "Regulation of the human growth hormone gene family: possible role for Pit-1 in early stages of pituitary-specific expression and repression". Neuroendocrinology 83 (3–4): 145–53. doi:10.1159/000095522. PMID 17047377. 
  • Li X, Giachelli CM (2007). "Sodium-dependent phosphate cotransporters and vascular calcification". Curr. Opin. Nephrol. Hypertens. 16 (4): 325–8. doi:10.1097/MNH.0b013e3281c55ef1. PMID 17565274. 
  • Tatsumi K, Miyai K, Notomi T et al. (1993). "Cretinism with combined hormone deficiency caused by a mutation in the PIT1 gene". Nat. Genet. 1 (1): 56–8. doi:10.1038/ng0492-56. PMID 1302000. 
  • Tatsumi K, Notomi T, Amino N, Miyai K (1992). "Nucleotide sequence of the complementary DNA for human Pit-1/GHF-1". Biochim. Biophys. Acta 1129 (2): 231–4. PMID 1370379. 
  • Ohta K, Nobukuni Y, Mitsubuchi H et al. (1993). "Mutations in the Pit-1 gene in children with combined pituitary hormone deficiency". Biochem. Biophys. Res. Commun. 189 (2): 851–5. doi:10.1016/0006-291X(92)92281-2. PMID 1472057. 
  • Ohta K, Nobukuni Y, Mitsubuchi H et al. (1993). "Characterization of the gene encoding human pituitary-specific transcription factor, Pit-1". Gene 122 (2): 387–8. doi:10.1016/0378-1119(92)90234-G. PMID 1487156. 
  • Radovick S, Nations M, Du Y et al. (1992). "A mutation in the POU-homeodomain of Pit-1 responsible for combined pituitary hormone deficiency". Science 257 (5073): 1115–8. doi:10.1126/science.257.5073.1115. PMID 1509262. 
  • Pfäffle RW, DiMattia GE, Parks JS et al. (1992). "Mutation of the POU-specific domain of Pit-1 and hypopituitarism without pituitary hypoplasia". Science 257 (5073): 1118–21. doi:10.1126/science.257.5073.1118. PMID 1509263. 
  • Lew AM, Elsholtz HP (1991). "Cloning of the human cDNA for transcription factor Pit-1". Nucleic Acids Res. 19 (22): 6329. doi:10.1093/nar/19.22.6329. PMC 329149. PMID 1956794. 
  • He X, Treacy MN, Simmons DM et al. (1989). "Expression of a large family of POU-domain regulatory genes in mammalian brain development". Nature 340 (6228): 35–41. doi:10.1038/340035a0. PMID 2739723. 
  • Bodner M, Castrillo JL, Theill LE et al. (1988). "The pituitary-specific transcription factor GHF-1 is a homeobox-containing protein". Cell 55 (3): 505–18. doi:10.1016/0092-8674(88)90037-2. PMID 2902927. 
  • Herr W, Sturm RA, Clerc RG et al. (1989). "The POU domain: a large conserved region in the mammalian pit-1, oct-1, oct-2, and Caenorhabditis elegans unc-86 gene products". Genes Dev. 2 (12A): 1513–6. doi:10.1101/gad.2.12a.1513. PMID 3215510. 
  • de Zegher F, Pernasetti F, Vanhole C et al. (1995). "The prenatal role of thyroid hormone evidenced by fetomaternal Pit-1 deficiency". J. Clin. Endocrinol. Metab. 80 (11): 3127–30. doi:10.1210/jc.80.11.3127. PMID 7593413. 
  • Bamberger AM, Bamberger CM, Pu LP et al. (1995). "Expression of pit-1 messenger ribonucleic acid and protein in the human placenta". J. Clin. Endocrinol. Metab. 80 (7): 2021–6. doi:10.1210/jc.80.7.2021. PMID 7608249. 
  • Irie Y, Tatsumi K, Ogawa M et al. (1995). "A novel E250X mutation of the PIT1 gene in a patient with combined pituitary hormone deficiency". Endocr. J. 42 (3): 351–4. doi:10.1507/endocrj.42.351. PMID 7670563. 
  • Delhase M, Vila V, Hooghe-Peters EL, Castrillo JL (1995). "A novel pituitary transcription factor is produced by alternative splicing of the human GHF-1/PIT-1 gene". Gene 155 (2): 273–5. doi:10.1016/0378-1119(94)00757-J. PMID 7721104. 
  • Okamoto N, Wada Y, Ida S et al. (1995). "Monoallelic expression of normal mRNA in the PIT1 mutation heterozygotes with normal phenotype and biallelic expression in the abnormal phenotype". Hum. Mol. Genet. 3 (9): 1565–8. doi:10.1093/hmg/3.9.1565. PMID 7833912. 

External links[edit]