Literature DB >> 8702665

Pseudohypoparathyroidism, a novel mutation in the betagamma-contact region of Gsalpha impairs receptor stimulation.

Z Farfel1, T Iiri, H Shapira, A Roitman, M Mouallem, H R Bourne.   

Abstract

Pseudohypoparathyroidism, type Ia (PHP-Ia), is a dominantly inherited endocrine disorder characterized by resistance to hormones that act by stimulating adenylyl cyclase. It is caused by inheritance of an autosomal mutation that inactivates the alpha subunit (alphas) of Gs, the stimulatory regulator of adenylyl cyclase. In three members of a family, the PHP-Ia phenotype is associated with a mutation (R231H) that substitutes histidine for an arginine at position 231 in alphas. We assessed signaling function of alphas-WT versus alphas-R231H transiently transfected in HEK293 cells. Hormone receptor-dependent stimulation of cAMP accumulation in cells expressing alphas-R231H is reduced by approximately 75% in comparison to cAMP accumulation in cells expressing alphas-WT. A second mutation, alphas-R201C, inhibits the GTPase turnoff reaction of alphas, thus producing receptor-independent stimulation of cAMP accumulation. The double mutant, alphas-R231H/R201C, stimulates cAMP accumulation almost as well (approximately 80%) as does alphas-R201C itself, indicating that the R231H mutation selectively impairs receptor-dependent signaling. In three-dimensional structures of G protein heterotrimers, Arg-231 is located in a region, switch 2, that is thought to interact with the betagamma subunit rather than with the hormone receptor. Thus, the R231H phenotype suggests that switch 2 (perhaps in concert with betagamma) mediates G protein activation by receptors at a site distant from the receptor-G protein contact surface.

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Year:  1996        PMID: 8702665     DOI: 10.1074/jbc.271.33.19653

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  9 in total

Review 1.  Multi-functionality of proteins involved in GPCR and G protein signaling: making sense of structure-function continuum with intrinsic disorder-based proteoforms.

Authors:  Alexander V Fonin; April L Darling; Irina M Kuznetsova; Konstantin K Turoverov; Vladimir N Uversky
Journal:  Cell Mol Life Sci       Date:  2019-08-19       Impact factor: 9.261

2.  Conditional activation defect of a human Gsalpha mutant.

Authors:  T Iiri; Z Farfel; H R Bourne
Journal:  Proc Natl Acad Sci U S A       Date:  1997-05-27       Impact factor: 11.205

3.  Human G(salpha) mutant causes pseudohypoparathyroidism type Ia/neonatal diarrhea, a potential cell-specific role of the palmitoylation cycle.

Authors:  Noriko Makita; Junichiro Sato; Philippe Rondard; Hiroshi Fukamachi; Yasuhito Yuasa; Micheala A Aldred; Makiko Hashimoto; Toshiro Fujita; Taroh Iiri
Journal:  Proc Natl Acad Sci U S A       Date:  2007-10-25       Impact factor: 11.205

4.  Diagnostic and mutational spectrum of progressive osseous heteroplasia (POH) and other forms of GNAS-based heterotopic ossification.

Authors:  N S Adegbite; M Xu; F S Kaplan; E M Shore; R J Pignolo
Journal:  Am J Med Genet A       Date:  2008-07-15       Impact factor: 2.802

5.  A universal allosteric mechanism for G protein activation.

Authors:  Kevin M Knight; Soumadwip Ghosh; Sharon L Campbell; Tyler J Lefevre; Reid H J Olsen; Alan V Smrcka; Natalie H Valentin; Guowei Yin; Nagarajan Vaidehi; Henrik G Dohlman
Journal:  Mol Cell       Date:  2021-02-25       Impact factor: 17.970

Review 6.  Progressive osseous heteroplasia: diagnosis, treatment, and prognosis.

Authors:  Robert J Pignolo; Girish Ramaswamy; John T Fong; Eileen M Shore; Frederick S Kaplan
Journal:  Appl Clin Genet       Date:  2015-01-30

7.  Identification of a novel GNAS mutation in a case of pseudohypoparathyroidism type 1A with normocalcemia.

Authors:  Xiao-Dan Long; Jing Xiong; Zhao-Hui Mo; Chang-Sheng Dong; Ping Jin
Journal:  BMC Med Genet       Date:  2018-07-30       Impact factor: 2.103

8.  Tertiary hyperparathyroidism in patients with pseudohypoparathyroidism type 1a.

Authors:  Masatsune Itoh; Michiko Okajima; Yuko Kittaka; Akihiro Yachie; Taizo Wada; Yutaka Saikawa
Journal:  Bone Rep       Date:  2022-04-14

9.  Case report: An infantile lethal form of Albright hereditary osteodystrophy due to a GNAS mutation.

Authors:  Valérie Leclercq; Valérie Benoit; Damien Lederer; Melanie Delaunoy; Marcela Ruiz; Claire de Halleux; Olivier Robaux; Catherine Wanty; Isabelle Maystadt
Journal:  Clin Case Rep       Date:  2018-08-16
  9 in total

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