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KidneyNetwork:利用肾脏来源的基因表达数据预测和优先考虑新的与肾脏疾病相关的基因。

KidneyNetwork: using kidney-derived gene expression data to predict and prioritize novel genes involved in kidney disease.

机构信息

Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Oncode Institute, Utrecht, The Netherlands.

出版信息

Eur J Hum Genet. 2023 Nov;31(11):1300-1308. doi: 10.1038/s41431-023-01296-x. Epub 2023 Feb 20.

DOI:10.1038/s41431-023-01296-x
PMID:36807342
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10620423/
Abstract

Genetic testing in patients with suspected hereditary kidney disease may not reveal the genetic cause for the disorder as potentially pathogenic variants can reside in genes that are not yet known to be involved in kidney disease. We have developed KidneyNetwork, that utilizes tissue-specific expression to inform candidate gene prioritization specifically for kidney diseases. KidneyNetwork is a novel method constructed by integrating a kidney RNA-sequencing co-expression network of 878 samples with a multi-tissue network of 31,499 samples. It uses expression patterns and established gene-phenotype associations to predict which genes could be related to what (disease) phenotypes in an unbiased manner. We applied KidneyNetwork to rare variants in exome sequencing data from 13 kidney disease patients without a genetic diagnosis to prioritize candidate genes. KidneyNetwork can accurately predict kidney-specific gene functions and (kidney disease) phenotypes for disease-associated genes. The intersection of prioritized genes with genes carrying rare variants in a patient with kidney and liver cysts identified ALG6 as plausible candidate gene. We strengthen this plausibility by identifying ALG6 variants in several cystic kidney and liver disease cases without alternative genetic explanation. We present KidneyNetwork, a publicly available kidney-specific co-expression network with optimized gene-phenotype predictions for kidney disease phenotypes. We designed an easy-to-use online interface that allows clinicians and researchers to use gene expression and co-regulation data and gene-phenotype connections to accelerate advances in hereditary kidney disease diagnosis and research. TRANSLATIONAL STATEMENT: Genetic testing in patients with suspected hereditary kidney disease may not reveal the genetic cause for the patient's disorder. Potentially pathogenic variants can reside in genes not yet known to be involved in kidney disease, making it difficult to interpret the relevance of these variants. This reveals a clear need for methods to predict the phenotypic consequences of genetic variation in an unbiased manner. Here we describe KidneyNetwork, a tool that utilizes tissue-specific expression to predict kidney-specific gene functions. Applying KidneyNetwork to a group of undiagnosed cases identified ALG6 as a candidate gene in cystic kidney and liver disease. In summary, KidneyNetwork can aid the interpretation of genetic variants and can therefore be of value in translational nephrogenetics and help improve the diagnostic yield in kidney disease patients.

摘要

在疑似遗传性肾脏疾病患者中进行基因检测可能无法揭示该疾病的遗传原因,因为潜在的致病性变异可能存在于尚未发现与肾脏疾病有关的基因中。我们开发了 KidneyNetwork,该工具利用组织特异性表达来专门针对肾脏疾病进行候选基因优先级排序。KidneyNetwork 是一种新方法,它通过整合 878 个样本的肾脏 RNA 测序共表达网络和 31499 个样本的多组织网络来构建。它使用表达模式和已建立的基因-表型关联来预测哪些基因可能与何种(疾病)表型相关,这是一种无偏倚的方法。我们将 KidneyNetwork 应用于 13 名无遗传诊断的肾脏疾病患者外显子测序数据中的罕见变异,以优先考虑候选基因。KidneyNetwork 可以准确预测与疾病相关基因的肾脏特异性基因功能和(肾脏疾病)表型。在一名患有肾和肝囊肿的患者中,将携带罕见变异的基因与优先级较高的基因进行交集,确定 ALG6 为可能的候选基因。通过在没有其他遗传解释的情况下在几个囊性肾脏和肝脏疾病病例中识别出 ALG6 变体,我们加强了这一可信度。我们提出了 KidneyNetwork,这是一种公开可用的肾脏特异性共表达网络,具有针对肾脏疾病表型的优化基因-表型预测。我们设计了一个易于使用的在线界面,允许临床医生和研究人员使用基因表达和共调控数据以及基因-表型连接来加速遗传性肾脏疾病的诊断和研究进展。

注

以上译文仅供参考,具体内容可根据实际情况进行调整。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b0/10620423/11b829d5a324/41431_2023_1296_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b0/10620423/4c5916b5c32d/41431_2023_1296_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b0/10620423/6d8f1548fe20/41431_2023_1296_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b0/10620423/a9f6b3116b3c/41431_2023_1296_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b0/10620423/11b829d5a324/41431_2023_1296_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b0/10620423/4c5916b5c32d/41431_2023_1296_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b0/10620423/6d8f1548fe20/41431_2023_1296_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b0/10620423/a9f6b3116b3c/41431_2023_1296_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10b0/10620423/11b829d5a324/41431_2023_1296_Fig4_HTML.jpg

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