Literature DB >> 12402266

A nonsense mutation of the MASS1 gene in a family with febrile and afebrile seizures.

Junko Nakayama1, Ying-Hui Fu, Anna M Clark, Satoko Nakahara, Kenzo Hamano, Nobuaki Iwasaki, Akira Matsui, Tadao Arinami, Louis J Ptácek.   

Abstract

A naturally occurring mutation of the mass1 (monogenic audiogenic seizure-susceptible) gene recently has been reported in the Frings mouse strain, which is prone to audiogenic seizures. The human orthologous gene, MASS1, was mapped to chromosome 5q14, for which we previously have reported significant evidence of linkage to febrile seizures (FEB4). We screened for MASS1 mutations in individuals from 48 families with familial febrile seizures and found 25 DNA alterations. None of nine missense polymorphic alleles was significantly associated with febrile seizures; however, a nonsense mutation (S2652X) causing a deletion of the C-terminal 126 amino acid residues was identified in one family with febrile and afebrile seizures. Our results suggest that a loss-of-function mutation in MASS1 might be responsible for the seizure phenotypes, though it is not likely that MASS1 contributed to the cause of febrile seizures in most of our families.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12402266     DOI: 10.1002/ana.10347

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


  43 in total

Review 1.  Autosomal dominant nocturnal frontal lobe epilepsy--a critical overview.

Authors:  Romina Combi; Leda Dalprà; Maria Luisa Tenchini; Luigi Ferini-Strambi
Journal:  J Neurol       Date:  2004-08       Impact factor: 4.849

Review 2.  Illuminating the Onco-GPCRome: Novel G protein-coupled receptor-driven oncocrine networks and targets for cancer immunotherapy.

Authors:  Victoria Wu; Huwate Yeerna; Nijiro Nohata; Joshua Chiou; Olivier Harismendy; Francesco Raimondi; Asuka Inoue; Robert B Russell; Pablo Tamayo; J Silvio Gutkind
Journal:  J Biol Chem       Date:  2019-06-05       Impact factor: 5.157

Review 3.  The very large G protein coupled receptor (Vlgr1) in hair cells.

Authors:  Jin-Peng Sun; Rong Li; Hong-Ze Ren; An-Ting Xu; Xiao Yu; Zhi-Gang Xu
Journal:  J Mol Neurosci       Date:  2012-11-20       Impact factor: 3.444

Review 4.  Chaperoning G protein-coupled receptors: from cell biology to therapeutics.

Authors:  Ya-Xiong Tao; P Michael Conn
Journal:  Endocr Rev       Date:  2014-03-24       Impact factor: 19.871

Review 5.  Adhesion G protein-coupled receptors in nervous system development and disease.

Authors:  Tobias Langenhan; Xianhua Piao; Kelly R Monk
Journal:  Nat Rev Neurosci       Date:  2016-07-28       Impact factor: 34.870

Review 6.  Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities.

Authors:  Pranav Mathur; Jun Yang
Journal:  Biochim Biophys Acta       Date:  2014-12-04

7.  Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family.

Authors:  Mounira Hmani-Aifa; Zeineb Benzina; Fareeha Zulfiqar; Houria Dhouib; Amber Shahzadi; Abdelmonem Ghorbel; Ahmed Rebaï; Peter Söderkvist; Sheikh Riazuddin; William J Kimberling; Hammadi Ayadi
Journal:  Eur J Hum Genet       Date:  2008-10-15       Impact factor: 4.246

8.  Expression studies in gliomas and glial cells do not support a tumor suppressor role for LGI1.

Authors:  Tiziana Piepoli; Cemile Jakupoglu; Wenli Gu; Elena Lualdi; Blanca Suarez-Merino; Pietro L Poliani; Maria Grazia Cattaneo; Barbara Ortino; Dorota Goplen; Jian Wang; Rosa Mola; Francesca Inverardi; Carolina Frassoni; Rolf Bjerkvig; Ortrud Steinlein; Lucia M Vicentini; Oliver Brüstle; Gaetano Finocchiaro
Journal:  Neuro Oncol       Date:  2006-03-02       Impact factor: 12.300

9.  Constitutive Gαi coupling activity of very large G protein-coupled receptor 1 (VLGR1) and its regulation by PDZD7 protein.

Authors:  Qiao-Xia Hu; Jun-Hong Dong; Hai-Bo Du; Dao-Lai Zhang; Hong-Ze Ren; Ming-Liang Ma; Yuan Cai; Tong-Chao Zhao; Xiao-Lei Yin; Xiao Yu; Tian Xue; Zhi-Gang Xu; Jin-Peng Sun
Journal:  J Biol Chem       Date:  2014-06-24       Impact factor: 5.157

10.  A large deletion in GPR98 causes type IIC Usher syndrome in male and female members of an Iranian family.

Authors:  N Hilgert; K Kahrizi; N Dieltjens; N Bazazzadegan; H Najmabadi; R J H Smith; G Van Camp
Journal:  J Med Genet       Date:  2009-04       Impact factor: 6.318

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.