Literature DB >> 27297032

Mutation/SNP analysis in EF-hand calcium binding domain of mitochondrial Ca[Formula: see text] uptake 1 gene in bipolar disorder patients.

Roghaiyeh Safari1, Reza Salimi2, Zeliha Tunca3, Aysegul Ozerdem3, Deniz Ceylan3, Meral Sakizli4.   

Abstract

Calcium signaling is important for synaptic plasticity, generation of brain rhythms, regulating neuronal excitability, data processing and cognition. Impairment in calcium homeostasis contributed to the development of psychiatric disorders such as bipolar disorder (BP). MCU is the most important calcium transporter in mitochondria inner membrane responsible for influx of Ca[Formula: see text]. MICU1 is linked with MCU and has two canonical EF hands that are vital for its activity and regulates MCU-mediated Ca[Formula: see text] influx. In the current study, we aimed to investigate the role of genetic alteration of EF hand calcium binding motifs of MICU1 on the development of BP. We examined patients with BP, first degree relatives of these patients and healthy volunteers for mutations and polymorphisms in EF hand calcium binding motifs of MICU1. The result showed no SNP/mutation in BP patients, in healthy subjects and in first degree relatives. Additionally, alignment of the EF hand calcium binding regions among species (Gallus-gallus, Canis-lupus-familiaris, Bos-taurus, Mus-musculus, Rattus-norvegicus, Pan-troglodytes, Homosapiens and Danio-rerio) showed exactly the same amino acids (DLNGDGEVDMEE and DCDGNGELSNKE) except in one of the calcium binding domain of Danio-rerio that there was only one difference; leucine instead of Methionine. Our results showed that the SNP on EF-hand Ca[Formula: see text] binding domains of MICU1 gene had no effect in phenotypic characters of BP patients.

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Keywords:  Bipolar disorder; EF-hand calcium binding domain; mitochondrial Ca uniporter; mitochondrial Ca uptake 1 (MICU1); mutation; single nucleotide polymorphism

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Year:  2016        PMID: 27297032     DOI: 10.1142/S0219635216500096

Source DB:  PubMed          Journal:  J Integr Neurosci        ISSN: 0219-6352            Impact factor:   2.117


  1 in total

1.  Reporting a rare form of myopathy, myopathy with extrapyramidal signs, in an Iranian family using next generation sequencing: a case report.

Authors:  Marzieh Mojbafan; Somayeh Takrim Nojehdeh; Faezeh Rahiminejad; Yalda Nilipour; Seyed Hasan Tonekaboni; Sirous Zeinali
Journal:  BMC Med Genet       Date:  2020-04-15       Impact factor: 2.103

  1 in total

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