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存档新生儿干血斑的RNA测序

RNA sequencing of archived neonatal dried blood spots.

作者信息

Bybjerg-Grauholm Jonas, Hagen Christian Munch, Khoo Sok Kean, Johannesen Maria Louise, Hansen Christine Søholm, Bækvad-Hansen Marie, Christiansen Michael, Hougaard David Michael, Hollegaard Mads V

机构信息

Department of Congenital Disorders, Statens Serum Institut, Copenhagen DK-2300, Denmark; iPSYCH, The Lundbeck Foundation Initiative for Integrative Psychiatric Research, Denmark.

Department of Cell and Molecular Biology, Grand Valley State University, Grand Rapids, MI 49503, USA.

出版信息

Mol Genet Metab Rep. 2016 Dec 24;10:33-37. doi: 10.1016/j.ymgmr.2016.12.004. eCollection 2017 Mar.

Abstract

Neonatal dried blood spots (DBS) are routinely collected on standard Guthrie cards for all-comprising national newborn screening programs for inborn errors of metabolism, hypothyroidism and other diseases. In Denmark, the Guthrie cards are stored at - 20 °C in the Danish Neonatal Screening Biobank and each sample is linked to elaborate social and medical registries. This provides a unique biospecimen repository to enable large population research at a perinatal level. Here, we demonstrate the feasibility to obtain gene expression data from DBS using next-generation RNA sequencing (RNA-seq). RNA-seq was performed on five males and five females. Sequencing results have an average of > 30 million reads per sample. 26,799 annotated features can be identified with 64% features detectable without fragments per kilobase of transcript per million mapped reads (FPKM) cutoff; number of detectable features dropped to 18% when FPKM ≥ 1. Sex can be discriminated using blood-based sex-specific gene set identified by the Genotype-Tissue Expression consortium. Here, we demonstrate the feasibility to acquire biologically-relevant gene expression from DBS using RNA-seq which provide a new avenue to investigate perinatal diseases in a high throughput manner.

摘要

在所有国家的新生儿筛查项目中,都会在标准的古思里卡片上常规采集新生儿干血斑(DBS),用于筛查先天性代谢缺陷、甲状腺功能减退症及其他疾病。在丹麦,古思里卡片保存在丹麦新生儿筛查生物样本库中,温度为-20°C,每个样本都与详细的社会和医疗登记信息相关联。这提供了一个独特的生物样本库,可用于围产期水平的大规模人群研究。在此,我们证明了使用下一代RNA测序(RNA-seq)从古思里卡片中获取基因表达数据的可行性。对五名男性和五名女性进行了RNA-seq检测。测序结果显示每个样本平均有超过3000万条读数。可识别出26799个注释特征,其中64%的特征在每百万映射读数中每千碱基转录本无片段(FPKM)截断值的情况下可检测到;当FPKM≥1时,可检测特征数量降至18%。可以使用基因型-组织表达联盟确定的基于血液的性别特异性基因集来区分性别。在此,我们证明了使用RNA-seq从古思里卡片中获取生物学相关基因表达的可行性,这为以高通量方式研究围产期疾病提供了一条新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcaa/5198792/28cf09802c5f/gr3.jpg

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