Literature DB >> 9050946

The molecular basis of disorders caused by defects in G proteins.

A M Spiegel1.   

Abstract

G proteins couple receptors for many hormones to effectors that regulate second messenger metabolism. G protein dysfunction could involve gain or loss of function. For Gs, the G protein that couples receptors to stimulation of cAMP formation, examples of both types have already been defined. Germline loss of function mutations in the Gs(alpha) gene are responsible for a form of inherited hormone resistance termed pseudohypoparathyroidism (Albright hereditary osteodystrophy). Conversely, somatic gain of function mutations cause constitutive stimulation of cAMP, independent of receptor activation, in acromegaly, in hyperfunctional thyroid nodules, and in the McCune-Albright syndrome. Future work is likely to uncover additional disorders caused by defective G proteins with implications for diagnosis and treatment.

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Year:  1997        PMID: 9050946     DOI: 10.1159/000185441

Source DB:  PubMed          Journal:  Horm Res        ISSN: 0301-0163


  12 in total

1.  Mutations in the gene encoding the alpha-subunit of the Gs protein in molar pregnancy.

Authors:  G Garon; J G LeHoux; P Bessette
Journal:  Endocrine       Date:  1999-08       Impact factor: 3.633

2.  Knockdown of PRKAR1A, the gene responsible for Carney complex, interferes with differentiation in osteoblastic cells.

Authors:  Mei Zhang; Parmeet K Manchanda; Dayong Wu; Qianben Wang; Lawrence S Kirschner
Journal:  Mol Endocrinol       Date:  2014-02-07

3.  G alpha(q) signal in osteoblasts is inhibitory to the osteoanabolic action of parathyroid hormone.

Authors:  Naoshi Ogata; Yusuke Shinoda; Nina Wettschureck; Stefan Offermanns; Shu Takeda; Kozo Nakamura; Gino V Segre; Ung-il Chung; Hiroshi Kawaguchi
Journal:  J Biol Chem       Date:  2011-02-23       Impact factor: 5.157

4.  Genetic analysis of the Drosophila Gs(alpha) gene.

Authors:  W J Wolfgang; A Hoskote; I J Roberts; S Jackson; M Forte
Journal:  Genetics       Date:  2001-07       Impact factor: 4.562

5.  A novel polymorphism at the GNAS1 gene associated with low circulating calcium levels.

Authors:  Laura Masi; Francesca Del Monte; Alessia Gozzini; Maria Laura De Feo; Riccardo Gionata Gheri; Annasilvia Neri; Alberto Falchetti; Antonietta Amedei; Rosario Imbriaco; Carmelo Mavilia; Annalisa Tanini; Maria Luisa Brandi
Journal:  Clin Cases Miner Bone Metab       Date:  2007-05

6.  Genetic diagnosis of multiple affected tissues in a patient with McCune-Albright syndrome.

Authors:  Ji Zhou; Li-hao Sun; Bin Cui; Huai-dong Song; Xiao-ying Li; Guang Ning; Jian-min Liu
Journal:  Endocrine       Date:  2007-04       Impact factor: 3.633

Review 7.  Neonatal thyroid disorders.

Authors:  A L Ogilvy-Stuart
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2002-11       Impact factor: 5.747

8.  An R201H activating mutation of the GNAS1 (Gsalpha) gene in a corticotroph pituitary adenoma.

Authors:  M Riminucci; M T Collins; R Lala; A Corsi; P Matarazzo; P Gehron Robey; P Bianco
Journal:  Mol Pathol       Date:  2002-02

9.  Constitutive expression of Gsα(R201C) in mice produces a heritable, direct replica of human fibrous dysplasia bone pathology and demonstrates its natural history.

Authors:  Isabella Saggio; Cristina Remoli; Emanuela Spica; Stefania Cersosimo; Benedetto Sacchetti; Pamela G Robey; Kenn Holmbeck; Ana Cumano; Alan Boyde; Paolo Bianco; Mara Riminucci
Journal:  J Bone Miner Res       Date:  2014-11       Impact factor: 6.741

10.  Reproduction of human fibrous dysplasia of bone in immunocompromised mice by transplanted mosaics of normal and Gsalpha-mutated skeletal progenitor cells.

Authors:  P Bianco; S A Kuznetsov; M Riminucci; L W Fisher; A M Spiegel; P G Robey
Journal:  J Clin Invest       Date:  1998-04-15       Impact factor: 14.808

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