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P r i n t / e x p o r t
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A p p e a r a n c e
F r o m W i k i p e d i a , t h e f r e e e n c y c l o p e d i a
Homeobox protein prophet of PIT-1 is a protein that in humans is encoded by the PROP1 gene .[5] [6]
PROP1 has both DNA-binding and transcriptional activation ability. Its expression leads to ontogenesis of pituitary gonadotropes, as well as somatotropes, lactotropes, and caudomedial thyrotropes. Inactivating mutations in PROP1 result in deficiencies of luteinizing hormone (LH; MIM 152780), follicle-stimulating hormone (FSH; MIM 136530), growth hormone (GH; MIM 139250), prolactin (PRL; MIM 176760), and thyroid-stimulating hormone (TSH; MIM 188540). See combined pituitary hormone deficiency (CPHD; MIM 262600).[supplied by OMIM][6]
References
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^ "Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ "Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ Wu W, Cogan JD, Pfaffle RW, Dasen JS, Frisch H, O'Connell SM, Flynn SE, Brown MR, Mullis PE, Parks JS, Phillips JA III, Rosenfeld MG (Feb 1998). "Mutations in PROP1 cause familial combined pituitary hormone deficiency". Nat Genet . 18 2 ): 147–9. doi :10.1038/ng0298-147 . PMID 9462743 . S2CID 6882625 .
^ a b "Entrez Gene: PROP1 prophet of Pit1, paired-like homeodomain transcription factor" .
Further reading
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Dasen JS, Rosenfeld MG (2001). "Signaling and transcriptional mechanisms in pituitary development". Annu. Rev. Neurosci . 24 1 ): 327–55. doi :10.1146/annurev.neuro.24.1.327 . PMID 11283314 . S2CID 19902876 .
Mody S, Brown MR, Parks JS (2003). "The spectrum of hypopituitarism caused by PROP1 mutations". Best Pract. Res. Clin. Endocrinol. Metab . 16 3 ): 421–31. doi :10.1053/beem.2002.0218 . PMID 12464226 .
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 .
Fofanova O, Takamura N, Kinoshita E, et al. (1998). "Compound heterozygous deletion of the PROP-1 gene in children with combined pituitary hormone deficiency" . J. Clin. Endocrinol. Metab . 83 7 ): 2601–4. doi :10.1210/jcem.83.7.5094 PMID 9661653 .
Amendt BA, Sutherland LB, Semina EV, Russo AF (1998). "The molecular basis of Rieger syndrome. Analysis of Pitx2 homeodomain protein activities" . J. Biol. Chem . 273 (32 ): 20066–72. doi :10.1074/jbc.273.32.20066 PMID 9685346 .
Cogan JD, Wu W, Phillips JA, et al. (1998). "The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency" (PDF) . J. Clin. Endocrinol. Metab . 83 9 ): 3346–9. doi :10.1210/jcem.83.9.5142 . hdl :10400.17/2282 PMID 9745452 .
Flück C, Deladoey J, Rutishauser K, et al. (1998). "Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitution of Arg→Cys at codon 120 (R120C)" . J. Clin. Endocrinol. Metab . 83 10 ): 3727–34. doi :10.1210/jcem.83.10.5172 PMID 9768691 . S2CID 10386868 .
Duquesnoy P, Roy A, Dastot F, et al. (1998). "Human Prop-1: cloning, mapping, genomic structure. Mutations in familial combined pituitary hormone deficiency" . FEBS Lett . 437 (3 ): 216–20. doi :10.1016/S0014-5793(98 )01234-4 PMID 9824293 . S2CID 20169741 .
Rosenbloom AL, Almonte AS, Brown MR, et al. (1999). "Clinical and biochemical phenotype of familial anterior hypopituitarism from mutation of the PROP1 gene" . J. Clin. Endocrinol. Metab . 84 1 ): 50–7. doi :10.1210/jcem.84.1.5366 PMID 9920061 . S2CID 35502053 .
Mendonca BB, Osorio MG, Latronico AC, et al. (1999). "Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 gene" . J. Clin. Endocrinol. Metab . 84 3 ): 942–5. doi :10.1210/jcem.84.3.5537 PMID 10084575 . S2CID 22748592 .
Nakamura Y, Usui T, Mizuta H, et al. (1999). "Characterization of Prophet of Pit-1 gene expression in normal pituitary and pituitary adenomas in humans" . J. Clin. Endocrinol. Metab . 84 4 ): 1414–9. doi :10.1210/jcem.84.4.5630 PMID 10199788 .
Deladoëy J, Flück C, Büyükgebiz A, et al. (1999). " . J. Clin. Endocrinol. Metab . 84 5 ): 1645–50. doi :10.1210/jcem.84.5.5681 PMID 10323394 . S2CID 2891639 .
Agarwal G, Bhatia V, Cook S, Thomas PQ (2001). "Adrenocorticotropin deficiency in combined pituitary hormone deficiency patients homozygous for a novel PROP1 deletion" . J. Clin. Endocrinol. Metab . 85 12 ): 4556–61. doi :10.1210/jcem.85.12.7013 PMID 11134108 .
Vallette-Kasic S, Barlier A, Teinturier C, et al. (2001). "PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiency" . J. Clin. Endocrinol. Metab . 86 9 ): 4529–35. doi :10.1210/jcem.86.9.7811 PMID 11549703 .
Teinturier C, Vallette S, Adamsbaum C, et al. (2002). "Pseudotumor of the pituitary due to PROP-1 deletion". J. Pediatr. Endocrinol. Metab . 15 1 ): 95–101. doi :10.1515/jpem.2002.15.1.95 . PMID 11822586 . S2CID 9184549 .
Crone J, Pfäffle R, Stobbe H, et al. (2002). "Familial combined pituitary hormone deficiency caused by PROP-1 gene mutation. Growth patterns and MRI studies in untreated subjects". Horm. Res . 57 doi :10.1159/000057962 . PMID 12006708 . S2CID 8619602 .
External links
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This article incorporates text from the United States National Library of Medicine , which is in the public domain .
t
e
(1 ) Basic domains
(1.1) Basic leucine zipper (bZIP )
(1.2) Basic helix-loop-helix (bHLH )
Group A
Group B
Group CPAS
Group D
Group E
Group F
(1.3) bHLH-ZIP
(1.4) NF-1
(1.5) RF-X
(1.6) Basic helix-span-helix (bHSH)
(2 ) Zinc finger DNA-binding domains
(2.1) Nuclear receptor (Cys4
subfamily 1
subfamily 2
subfamily 3
subfamily 4
subfamily 5
subfamily 6
subfamily 0
(2.2) Other Cys4
(2.3) Cys2 2
(2.4) Cys6
(2.5) Alternating composition
(2.6) WRKY
(4 ) β-Scaffold factors with minor groove contacts
(0) Other transcription factors
see also transcription factor/coregulator deficiencies
t
e
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● T h i s p a g e w a s l a s t e d i t e d o n 8 A p r i l 2 0 2 4 , a t 2 2 : 1 2 ( U T C ) . ● T e x t i s a v a i l a b l e u n d e r t h e C r e a t i v e C o m m o n s A t t r i b u t i o n - S h a r e A l i k e L i c e n s e 4 . 0 ;
a d d i t i o n a l t e r m s m a y a p p l y . B y u s i n g t h i s s i t e , y o u a g r e e t o t h e T e r m s o f U s e a n d P r i v a c y P o l i c y . W i k i p e d i a ® i s a r e g i s t e r e d t r a d e m a r k o f t h e W i k i m e d i a F o u n d a t i o n , I n c . , a n o n - p r o f i t o r g a n i z a t i o n . ● P r i v a c y p o l i c y ● A b o u t W i k i p e d i a ● D i s c l a i m e r s ● C o n t a c t W i k i p e d i a ● C o d e o f C o n d u c t ● D e v e l o p e r s ● S t a t i s t i c s ● C o o k i e s t a t e m e n t ● M o b i l e v i e w
