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与微小RNA改变相关的X染色体精神分裂症的证据。

Evidence for X-chromosomal schizophrenia associated with microRNA alterations.

作者信息

Feng Jinong, Sun Guihua, Yan Jin, Noltner Katie, Li Wenyan, Buzin Carolyn H, Longmate Jeff, Heston Leonard L, Rossi John, Sommer Steve S

机构信息

Division of Molecular Genetics, City of Hope National Medical Center, Duarte, CA, USA.

出版信息

PLoS One. 2009 Jul 1;4(7):e6121. doi: 10.1371/journal.pone.0006121.

Abstract

BACKGROUND

Schizophrenia is a severe disabling brain disease affecting about 1% of the population. Individual microRNAs (miRNAs) affect moderate downregulation of gene expression. In addition, components required for miRNA processing and/or function have also been implicated in X-linked mental retardation, neurological and neoplastic diseases, pointing to the wide ranging involvement of miRNAs in disease.

METHODS AND FINDINGS

To explore the role of miRNAs in schizophrenia, 59 microRNA genes on the X-chromosome were amplified and sequenced in males with (193) and without (191) schizophrenia spectrum disorders to test the hypothesis that ultra-rare mutations in microRNA collectively contribute to the risk of schizophrenia. Here we provide the first association of microRNA gene dysfunction with schizophrenia. Eight ultra-rare variants in the precursor or mature miRNA were identified in eight distinct miRNA genes in 4% of analyzed males with schizophrenia. One ultra-rare variant was identified in a control sample (with a history of depression) (8/193 versus 1/191, p = 0.02 by one-sided Fisher's exact test, odds ratio = 8.2). These variants were not found in an additional 7,197 control X-chromosomes.

CONCLUSIONS

Functional analyses of ectopically expressed copies of the variant miRNA precursors demonstrate loss of function, gain of function or altered expression levels. While confirmation is required, this study suggests that microRNA mutations can contribute to schizophrenia.

摘要

背景

精神分裂症是一种严重的致残性脑部疾病,影响约1%的人口。单个微小RNA(miRNA)影响基因表达的适度下调。此外,miRNA加工和/或功能所需的成分也与X连锁智力迟钝、神经和肿瘤疾病有关,这表明miRNA广泛参与疾病过程。

方法与发现

为了探究miRNA在精神分裂症中的作用,对患有(193例)和未患有(191例)精神分裂症谱系障碍的男性的X染色体上的59个微小RNA基因进行了扩增和测序,以检验微小RNA中的超罕见突变共同导致精神分裂症风险的假设。在此,我们首次报道了微小RNA基因功能障碍与精神分裂症的关联。在4%的分析的患有精神分裂症的男性中,在8个不同的微小RNA基因中鉴定出前体或成熟miRNA中的八个超罕见变异。在一个对照样本(有抑郁症病史)中鉴定出一个超罕见变异(193例中有8例,191例中有1例,单侧Fisher精确检验p = 0.02,优势比 = 8.2)。在另外7197条对照X染色体中未发现这些变异。

结论

对变异miRNA前体的异位表达拷贝进行功能分析,显示出功能丧失、功能获得或表达水平改变。虽然需要进一步证实,但本研究表明微小RNA突变可能导致精神分裂症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9920/2699475/b01d8a8f2141/pone.0006121.g001.jpg

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