Resau James H, Ho Nhan T, Dykema Karl, Faber Matthew S, Busik Julia V, Nickolov Radoslav Z, Furge Kyle A, Paneth Nigel, Jewell Scott, Khoo Sok Kean
Program of Biospecimen Science, Van Andel Research Institute, Grand Rapids, MI 49503, USA.
Department of Epidemiology & Biostatistics, College of Human Medicine, Michigan State University, East Lansing, MI 48823, USA.
Int J Mol Sci. 2012;13(8):9599-9608. doi: 10.3390/ijms13089599. Epub 2012 Aug 2.
Screening newborns for treatable serious conditions is mandated in all US states and many other countries. After screening, Guthrie cards with residual blood (whole spots or portions of spots) are typically stored at ambient temperature in many facilities. The potential of archived dried blood spots (DBS) for at-birth molecular studies in epidemiological and clinical research is substantial. However, it is also challenging as analytes from DBS may be degraded due to preparation and storage conditions. We previously reported an improved assay for obtaining global RNA gene expression from blood spots. Here, we evaluated sex-specific gene expression and its preservation in DBS using oligonucleotide microarray technology. We found X inactivation-specific transcript (XIST), lysine-specific demethylase 5D (KDM5D) (also known as selected cDNA on Y, homolog of mouse (SMCY)), uncharacterized LOC729444 (LOC729444), and testis-specific transcript, Y-linked 21 (TTTY21) to be differentially-expressed by sex of the newborn. Our finding that trait-specific RNA gene expression is preserved in unfrozen DBS, demonstrates the technical feasibility of performing molecular genetic profiling using such samples. With millions of DBS potentially available for research, we see new opportunities in using newborn molecular gene expression to better understand molecular pathogenesis of perinatal diseases.
美国所有州及许多其他国家都规定要对新生儿进行可治疗严重疾病的筛查。筛查后,许多机构通常将带有残余血液(整个血斑或部分血斑)的格思里卡片在室温下保存。存档干血斑(DBS)在流行病学和临床研究的出生时分子研究中的潜力巨大。然而,这也具有挑战性,因为DBS中的分析物可能会因制备和储存条件而降解。我们之前报道了一种从血斑中获得全局RNA基因表达的改进检测方法。在此,我们使用寡核苷酸微阵列技术评估了DBS中性别特异性基因表达及其保存情况。我们发现X染色体失活特异性转录本(XIST)、赖氨酸特异性去甲基化酶5D(KDM5D)(也称为Y染色体上的选定cDNA,小鼠同源物(SMCY))、未表征的LOC729444(LOC729444)和睾丸特异性转录本Y连锁21(TTTY21)在新生儿中存在性别差异表达。我们的发现,即未冷冻的DBS中保留了性状特异性RNA基因表达,证明了使用此类样本进行分子遗传分析的技术可行性。由于有数以百万计的DBS可能可用于研究,我们看到了利用新生儿分子基因表达来更好地理解围产期疾病分子发病机制的新机会。