Literature DB >> 31860119

Shortened Fingers and Toes: GNAS Abnormalities are Not the Only Cause.

Monica Reyes1, Caroline Silve2,3,4, Harald Jüppner1,5.   

Abstract

The PTH/PTHrP receptor (PTHR1) mediates the actions of parathyroid hormone (PTH) and PTH-related peptide (PTHrP) by coupling this G protein-coupled receptor (GPCR) to the alpha-subunit of the heterotrimeric stimulatory G protein (Gsα) and thereby to the formation of cAMP. In growth plates, PTHrP-dependent activation of the cAMP/PKA second messenger pathway prevents the premature differentiation of chondrocytes into hypertrophic cells resulting in delayed growth plate closure. Heterozygous mutations in GNAS, the gene encoding Gsα, lead to a reduction in cAMP levels in growth plate chondrocytes that is sufficient to cause shortening of metacarpals and/or -tarsals, i. e. typical skeletal aspects of Albright's Hereditary Osteodystrophy (AHO). However, heterozygous mutations in other genes, including those encoding PTHrP, PRKAR1A, PDE4D, and PDE3A, can lead to similar or even more pronounced acceleration of skeletal maturation that is particularly obvious in hands and feet, and reduces final adult height. Genetic mutations other than those resulting in Gsα haploinsufficiency thus reduce intracellular cAMP levels in growth plate chondrocytes to a similar extent and thereby accelerate skeletal maturation. Thieme. All rights reserved.

Entities:  

Year:  2019        PMID: 31860119      PMCID: PMC7950720          DOI: 10.1055/a-1047-0334

Source DB:  PubMed          Journal:  Exp Clin Endocrinol Diabetes        ISSN: 0947-7349            Impact factor:   2.949


  68 in total

1.  GNAS1 lesions in pseudohypoparathyroidism Ia and Ic: genotype phenotype relationship and evidence of the maternal transmission of the hormonal resistance.

Authors:  Agnès Linglart; Jean Claude Carel; Michèle Garabédian; Tran Lé; Eric Mallet; Marie Laure Kottler
Journal:  J Clin Endocrinol Metab       Date:  2002-01       Impact factor: 5.958

2.  Deficient activity of guanine nucleotide regulatory protein in erythrocytes from patients with pseudohypoparathyroidism.

Authors:  M A Levine; R W Downs; M Singer; S J Marx; G D Aurbach; A M Spiegel
Journal:  Biochem Biophys Res Commun       Date:  1980-06-30       Impact factor: 3.575

Review 3.  cAMP-dependent protein kinase: framework for a diverse family of regulatory enzymes.

Authors:  S S Taylor; J A Buechler; W Yonemoto
Journal:  Annu Rev Biochem       Date:  1990       Impact factor: 23.643

4.  Parathyroid function and the renal excretion of 3'5'-adenylic acid.

Authors:  L R Chase; G D Aurbach
Journal:  Proc Natl Acad Sci U S A       Date:  1967-08       Impact factor: 11.205

5.  Albright hereditary osteodystrophy and del(2) (q37.3) in four unrelated individuals.

Authors:  M C Phelan; R C Rogers; K B Clarkson; F P Bowyer; M A Levine; L L Estabrooks; M C Severson; W B Dobyns
Journal:  Am J Med Genet       Date:  1995-07-31

6.  Engineered stabilization and structural analysis of the autoinhibited conformation of PDE4.

Authors:  Peder Cedervall; Ann Aulabaugh; Kieran F Geoghegan; Thomas J McLellan; Jayvardhan Pandit
Journal:  Proc Natl Acad Sci U S A       Date:  2015-03-09       Impact factor: 11.205

7.  Pseudohypoparathyroidism: defective excretion of 3',5'-AMP in response to parathyroid hormone.

Authors:  L R Chase; G L Melson; G D Aurbach
Journal:  J Clin Invest       Date:  1969-10       Impact factor: 14.808

8.  Defect of receptor-cyclase coupling protein in psudohypoparathyroidism.

Authors:  Z Farfel; A S Brickman; H R Kaslow; V M Brothers; H R Bourne
Journal:  N Engl J Med       Date:  1980-07-31       Impact factor: 91.245

Review 9.  Report of two novel mutations in PTHLH associated with brachydactyly type E and literature review.

Authors:  Cecile Thomas-Teinturier; Arrate Pereda; Intza Garin; Ignacio Diez-Lopez; Agnès Linglart; Caroline Silve; Guiomar Pérez de Nanclares
Journal:  Am J Med Genet A       Date:  2015-12-06       Impact factor: 2.802

Review 10.  The brachydactylies: a molecular disease family.

Authors:  S Mundlos
Journal:  Clin Genet       Date:  2009-08       Impact factor: 4.438

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