Archived Unfrozen Neonatal Blood Spots Are Amenable to Quantitative Gene Expression Analysis

被引:24
作者
Haak, Peterson T. [1 ,3 ,5 ]
Busik, Julia V. [6 ]
Kort, Eric J. [2 ]
Tikhonenko, Maria [6 ]
Paneth, Nigel [3 ,4 ]
Resau, James H. [1 ,2 ]
机构
[1] Van Andel Res Inst, Lab Microarray Technol, Grand Rapids, MI 49503 USA
[2] Van Andel Res Inst, Lab Mol Epidemiol, Grand Rapids, MI 49503 USA
[3] Michigan State Univ, Dept Epidemiol, Coll Human Med, E Lansing, MI 48824 USA
[4] Michigan State Univ, Dept Pediat & Human Dev, Coll Human Med, E Lansing, MI 48824 USA
[5] Michigan State Univ, Coll Osteopath Med, E Lansing, MI 48824 USA
[6] Michigan State Univ, Dept Physiol, E Lansing, MI 48824 USA
关键词
Guthrie; Blood spot; RNA; Microarray; qPCR; Real-time PCR; Neonatal screening; POLYMERASE-CHAIN-REACTION; ACUTE LYMPHOBLASTIC-LEUKEMIA; CDNA MICROARRAY DATA; DRIED-BLOOD; FILTER-PAPER; MESSENGER-RNA; DNA; SAMPLES; AMPLIFICATION; PCR;
D O I
10.1159/000155652
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: State laws in the USA mandate that blood be drawn from all newborn infants to screen for health-threatening conditions. These screening assays consume only a small portion of the blood samples, which are collected on filter paper ('Guthrie') cards. Many states archive unused blood spots, often in unrefrigerated storage. Objectives: While individual RNA transcripts have been identified from archived neonatal blood spots, no study to date has performed quantitative analysis of archived blood spot RNA. Methods: We demonstrate that RNA can be isolated and amplified from newborn blood spots stored unfrozen for as long as 9 years, and can be analyzed by microarray and qPCR. Results: Microarray assays of archived neonatal blood spots consistently detected 3,000-4,000 expressed genes with correlations of 0.90 between replicates. Blood spot mRNA is amenable to qPCR and we detected biologically relevant expression levels of housekeeping and immune-mediating genes. Conclusions: These experiments demonstrate the feasibility of using blood spots as a source of RNA which can be analyzed using quantitative microarray and qPCR assays. The application of these methods to the analysis of widely collected biological specimens may be a valuable resource for the study of perinatal determinants of disease development. Copyright (C) 2008 S. Karger AG, Basel
引用
收藏
页码:210 / 216
页数:7
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