1 《公共科学图书馆•综合》2011年1 6:e20468
PMID 21674006
Title Genome-wide association study of schizophrenia in Japanese population.
Abstract schizophreniais a devastating neuropsychiatric disorder with genetically complex traits. Genetic variants should explain a considerable portion of the risk forschizophrenia,and genome-wide association study (GWAS) is a potentially powerful tool for identifying the risk variants that underlie the disease. Here, we report the results of a three-stage analysis of three independent cohorts consisting of a total of 2,535 samples from Japanese and Chinese populations for searchingschizophreniasusceptibility genes using a GWAS approach. Firstly, we examined 115,770 single nucleotide polymorphisms (SNPs) in 120 patient-parents trio samples from Japaneseschizophreniapedigrees. In stage II, we evaluated 1,632 SNPs (1,159 SNPs of p<0.01 and 473 SNPs of p<0.05 that located in previously reported linkage regions). The second sample consisted of 1,012 case-control samples of Japanese origin. The most significant p value was obtained for the SNP in theELAVL2[(embryonic lethal, abnormal vision, Drosophila)-like 2] gene located on 9p21.3 (p?=?0.00087). In stage III, we scrutinized theELAVL2gene by genotyping gene-centric tagSNPs in the third sample set of 293 family samples (1,163 individuals) of Chinese descent and the SNP in the gene showed a nominal association withschizophreniain Chinese population (p?=?0.026). The current data in Asian population would be helpful for deciphering ethnic diversity ofschizophreniaetiology.
SCZ Keywords schizophrenia
2 Biochem. Biophys. Res. Commun. 2015 Oct 466: 46-51
PMID 26325429
Title Acute reduction of neuronal RNA binding Elavl2 protein and Gap43 mRNA in mouse hippocampus after kainic acid treatment.
Abstract Activity-dependent gene regulation in neurons has been hypothesized to be under transcriptional control and to include dramatic increases in immediate early genes (IEGs) after neuronal activity. In addition, several reports have focused on post-transcriptional regulation, which could be mediated by neuronal post-transcriptional regulators, including RNA binding proteins (RNABPs). One such protein family is the neuronal Elavls (nElavls;ELAVL2,Elavl3, and Elavl4), whose members are widely expressed in peripheral and central nervous system. Previous reports showed that Elavl3 and 4 are up-regulated following repeated stimulation such as during cocaine administration, a seizure, or a spatial discrimination task. In this study, we focused onELAVL2,a candidate gene forschizophreniaand studied its role in neuronal activity. First we found thatELAVL2has a cell-type specific expression pattern that is highly expressed in hippocampal CA3 pyramidal neurons and hilar interneurons usingELAVL2specific antibody. Second, unexpectedly, we discovered that theELAVL2protein level in the hippocampus was acutely down-regulated for 3 h after a kainic acid (KA)-induced seizure in the hippocampal CA3 region. In addition, level of Gap43 mRNA, a target mRNA ofELAVL2is decreased 12 h after KA treatment, thus suggesting the involvement ofELAVL2in activity-dependent RNA regulation.
SCZ Keywords schizophrenia
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