Literature DB >> 19847910

Calcium/calmodulin-dependent serine protein kinase and mental retardation.

Yi-Ping Hsueh1.   

Abstract

Calcium/calmodulin-dependent serine protein kinase (CASK) belongs to the membrane-associated guanylate kinase protein family. The members of this protein family function as multiple domain adaptor proteins originally identified at cell junctions and synapses. Insertional mutations or targeted disruption of the CASK gene in mice results in neonatal lethality, indicating an important role for CASK in development. Recently, several reports have also indicated that mutations in the human CASK gene result in X-linked malformations of the brain and mental retardation. At the molecular level, many studies indicate that CASK is critical for synapse formation at both presynaptic and postsynaptic junctions, and in the regulation of gene expression. The known molecular functions of CASK explain, at least partially, mental retardation and brain developmental defects in patients. In this review, recent findings about CASK are summarized and discussed.

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Year:  2009        PMID: 19847910     DOI: 10.1002/ana.21755

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  33 in total

Review 1.  MAGUKs, synaptic development, and synaptic plasticity.

Authors:  Chan-Ying Zheng; Gail K Seabold; Martin Horak; Ronald S Petralia
Journal:  Neuroscientist       Date:  2011-04-15       Impact factor: 7.519

2.  Novel intragenic duplications and mutations of CASK in patients with mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH).

Authors:  Shin Hayashi; Nobuhiko Okamoto; Yasutsugu Chinen; Jun-ichi Takanashi; Yoshio Makita; Akira Hata; Issei Imoto; Johji Inazawa
Journal:  Hum Genet       Date:  2011-07-07       Impact factor: 4.132

3.  Neuroradiologic features of CASK mutations.

Authors:  J Takanashi; H Arai; S Nabatame; S Hirai; S Hayashi; J Inazawa; N Okamoto; A J Barkovich
Journal:  AJNR Am J Neuroradiol       Date:  2010-07-01       Impact factor: 3.825

4.  The molecular basis of the Caskin1 and Mint1 interaction with CASK.

Authors:  Ryan L Stafford; Jason Ear; Mary Jane Knight; James U Bowie
Journal:  J Mol Biol       Date:  2011-07-12       Impact factor: 5.469

5.  Tandem SAM domain structure of human Caskin1: a presynaptic, self-assembling scaffold for CASK.

Authors:  Ryan L Stafford; Elizabeth Hinde; Mary Jane Knight; Mario A Pennella; Jason Ear; Michelle A Digman; Enrico Gratton; James U Bowie
Journal:  Structure       Date:  2011-12-07       Impact factor: 5.006

6.  Spectrum of pontocerebellar hypoplasia in 13 girls and boys with CASK mutations: confirmation of a recognizable phenotype and first description of a male mosaic patient.

Authors:  Lydie Burglen; Sandra Chantot-Bastaraud; Catherine Garel; Mathieu Milh; Renaud Touraine; Ginevra Zanni; Florence Petit; Alexandra Afenjar; Cyril Goizet; Sabina Barresi; Aurélie Coussement; Christine Ioos; Leila Lazaro; Sylvie Joriot; Isabelle Desguerre; Didier Lacombe; Vincent des Portes; Enrico Bertini; Jean-Pierre Siffroi; Thierry Billette de Villemeur; Diana Rodriguez
Journal:  Orphanet J Rare Dis       Date:  2012-03-27       Impact factor: 4.123

7.  Calcium/calmodulin-dependent serine protein kinase (CASK), a protein implicated in mental retardation and autism-spectrum disorders, interacts with T-Brain-1 (TBR1) to control extinction of associative memory in male mice.

Authors:  Tzyy-Nan Huang; Yi-Ping Hsueh
Journal:  J Psychiatry Neurosci       Date:  2017-01       Impact factor: 6.186

8.  Novel CASK mutations in cases with syndromic microcephaly.

Authors:  Francesca Cristofoli; Koen Devriendt; Erica E Davis; Hilde Van Esch; Joris R Vermeesch
Journal:  Hum Mutat       Date:  2018-05-11       Impact factor: 4.878

Review 9.  X-linked disorders with cerebellar dysgenesis.

Authors:  Ginevra Zanni; Enrico S Bertini
Journal:  Orphanet J Rare Dis       Date:  2011-05-15       Impact factor: 4.123

10.  Mutation of plasma membrane Ca2+ ATPase isoform 3 in a family with X-linked congenital cerebellar ataxia impairs Ca2+ homeostasis.

Authors:  Ginevra Zanni; Tito Calì; Vera M Kalscheuer; Denis Ottolini; Sabina Barresi; Nicolas Lebrun; Luisa Montecchi-Palazzi; Hao Hu; Jamel Chelly; Enrico Bertini; Marisa Brini; Ernesto Carafoli
Journal:  Proc Natl Acad Sci U S A       Date:  2012-08-21       Impact factor: 11.205

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