Literature DB >> 30197841

Inositol 1,4,5-trisphosphate Receptor Mutations associated with Human Disease.

Lara E Terry1, Kamil J Alzayady1, Esraa Furati1, David I Yule1.   

Abstract

Calcium release into the cytosol via the inositol 1,4,5-trisphosphate receptor (IP3R) calcium channel is important for a variety of cellular processes. As a result, impairment or inhibition of this release can result in disease. Recently, mutations in all four domains of the IP3R have been suggested to cause diseases such as ataxia, cancer, and anhidrosis; however, most of these mutations have not been functionally characterized. In this review we summarize the reported mutations, as well as the associated symptoms. Additionally, we use clues from transgenic animals, receptor stoichiometry, and domain location of mutations to speculate on the effects of individual mutations on receptor structure and function and the overall mechanism of disease.

Entities:  

Year:  2018        PMID: 30197841      PMCID: PMC6128530     

Source DB:  PubMed          Journal:  Messenger (Los Angel)


  71 in total

1.  Unique Regulatory Properties of Heterotetrameric Inositol 1,4,5-Trisphosphate Receptors Revealed by Studying Concatenated Receptor Constructs.

Authors:  Rahul Chandrasekhar; Kamil J Alzayady; Larry E Wagner; David I Yule
Journal:  J Biol Chem       Date:  2016-01-11       Impact factor: 5.157

2.  IP3 receptor types 2 and 3 mediate exocrine secretion underlying energy metabolism.

Authors:  Akira Futatsugi; Takeshi Nakamura; Maki K Yamada; Etsuko Ebisui; Kyoko Nakamura; Keiko Uchida; Tetsuya Kitaguchi; Hiromi Takahashi-Iwanaga; Tetsuo Noda; Jun Aruga; Katsuhiko Mikoshiba
Journal:  Science       Date:  2005-09-30       Impact factor: 47.728

3.  Motor behavior of heterozygous staggerer mutant (+/sg) versus normal (+/+) mice during aging.

Authors:  J Caston; N Delhaye-Bouchaud; J Mariani
Journal:  Behav Brain Res       Date:  1995-12-14       Impact factor: 3.332

4.  Additional features of Gillespie syndrome in two Brazilian siblings with a novel ITPR1 homozygous pathogenic variant.

Authors:  Daniel R Carvalho; João Eugenio G Medeiros; Daniela Sebestyan M Ribeiro; Bernardo J A F Martins; Nara L M Sobreira
Journal:  Eur J Med Genet       Date:  2017-11-21       Impact factor: 2.708

5.  Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxia.

Authors:  Brent L Fogel; Hane Lee; Joshua L Deignan; Samuel P Strom; Sibel Kantarci; Xizhe Wang; Fabiola Quintero-Rivera; Eric Vilain; Wayne W Grody; Susan Perlman; Daniel H Geschwind; Stanley F Nelson
Journal:  JAMA Neurol       Date:  2014-10       Impact factor: 18.302

6.  Cerebellar Purkinje cell loss during life span of the heterozygous staggerer mouse (Rora(+)/Rora(sg)) is gender-related.

Authors:  M Doulazmi; F Frédéric; Y Lemaigre-Dubreuil; N Hadj-Sahraoui; N Delhaye-Bouchaud; J Mariani
Journal:  J Comp Neurol       Date:  1999-08-23       Impact factor: 3.215

7.  Structure of the inositol 1,4,5-trisphosphate receptor binding core in complex with its ligand.

Authors:  Ivan Bosanac; Jean-René Alattia; Tapas K Mal; Jenny Chan; Susanna Talarico; Frances K Tong; Kit I Tong; Fumio Yoshikawa; Teiichi Furuichi; Miwako Iwai; Takayuki Michikawa; Katsuhiko Mikoshiba; Mitsuhiko Ikura
Journal:  Nature       Date:  2002-11-17       Impact factor: 49.962

8.  Development of a multiplex ligation-dependent probe amplification assay for diagnosis and estimation of the frequency of spinocerebellar ataxia type 15.

Authors:  Devika Ganesamoorthy; Damien L Bruno; Jacqueline Schoumans; Elsdon Storey; Martin B Delatycki; Danqing Zhu; Morgan K Wei; Garth A Nicholson; R J McKinlay Gardner; Howard R Slater
Journal:  Clin Chem       Date:  2009-05-07       Impact factor: 8.327

9.  Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia.

Authors:  Yasmin Namavar; Peter G Barth; Paul R Kasher; Fred van Ruissen; Knut Brockmann; Günther Bernert; Karin Writzl; Karen Ventura; Edith Y Cheng; Donna M Ferriero; Lina Basel-Vanagaite; Veerle R C Eggens; Ingeborg Krägeloh-Mann; Linda De Meirleir; Mary King; John M Graham; Arpad von Moers; Nine Knoers; Laszlo Sztriha; Rudolf Korinthenberg; William B Dobyns; Frank Baas; Bwee Tien Poll-The
Journal:  Brain       Date:  2010-10-15       Impact factor: 15.255

10.  CA8 mutations cause a novel syndrome characterized by ataxia and mild mental retardation with predisposition to quadrupedal gait.

Authors:  Seval Türkmen; Gao Guo; Masoud Garshasbi; Katrin Hoffmann; Amjad J Alshalah; Claudia Mischung; Andreas Kuss; Nicholas Humphrey; Stefan Mundlos; Peter N Robinson
Journal:  PLoS Genet       Date:  2009-05-22       Impact factor: 6.020

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  7 in total

Review 1.  Structure and Function of IP3 Receptors.

Authors:  David L Prole; Colin W Taylor
Journal:  Cold Spring Harb Perspect Biol       Date:  2019-04-01       Impact factor: 10.005

Review 2.  The Targeting of Native Proteins to the Endoplasmic Reticulum-Associated Degradation (ERAD) Pathway: An Expanding Repertoire of Regulated Substrates.

Authors:  Deepa Kumari; Jeffrey L Brodsky
Journal:  Biomolecules       Date:  2021-08-11

3.  Structural basis for activation and gating of IP3 receptors.

Authors:  Emily A Schmitz; Hirohide Takahashi; Erkan Karakas
Journal:  Nat Commun       Date:  2022-03-17       Impact factor: 14.919

4.  Cryo-EM structure of type 1 IP3R channel in a lipid bilayer.

Authors:  Mariah R Baker; Guizhen Fan; Alexander B Seryshev; Melina A Agosto; Matthew L Baker; Irina I Serysheva
Journal:  Commun Biol       Date:  2021-05-25

5.  Ca2+ signaling in T lymphocytes: the interplay of the endoplasmic reticulum, mitochondria, membrane potential, and CRAC channels on transcription factor activation.

Authors:  Pei-Chi Yang; M Saleet Jafri
Journal:  Heliyon       Date:  2020-03-07

6.  Modulation of flight and feeding behaviours requires presynaptic IP3Rs in dopaminergic neurons.

Authors:  Anamika Sharma; Gaiti Hasan
Journal:  Elife       Date:  2020-11-06       Impact factor: 8.140

7.  Disease-associated mutations in inositol 1,4,5-trisphosphate receptor subunits impair channel function.

Authors:  Lara E Terry; Kamil J Alzayady; Amanda M Wahl; Sundeep Malik; David I Yule
Journal:  J Biol Chem       Date:  2020-10-22       Impact factor: 5.157

  7 in total

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