Ho Nhan T, Busik Julia V, Resau James H, Paneth Nigel, Khoo Sok Kean
Department of Epidemiology & Biostatistics, College of Human Medicine, Michigan State University, East Lansing, MI, USA.
Department of Physiology, Michigan State University, East Lansing, MI, USA.
Mol Genet Metab. 2016 Nov;119(3):207-213. doi: 10.1016/j.ymgme.2016.08.001. Epub 2016 Aug 18.
Unfrozen archived newborn blood spots (NBS) have been shown to retain sufficient messenger RNA (mRNA) for gene expression profiling. However, the effect of storage time at ambient temperature for NBS samples in relation to the quality of gene expression data is relatively unknown. Here, we evaluated mRNA expression from quantitative real-time PCR (qRT-PCR) and microarray data obtained from NBS samples stored at ambient temperature to determine the effect of storage time on the quality of gene expression. These data were generated in a previous case-control study examining NBS in 53 children with cerebral palsy (CP) and 53 matched controls. NBS sample storage period ranged from 3 to 16years at ambient temperature. We found persistently low RNA integrity numbers (RIN=2.3±0.71) and 28S/18S rRNA ratios (~0) across NBS samples for all storage periods. In both qRT-PCR and microarray data, the expression of three common housekeeping genes-beta cytoskeletal actin (ACTB), glyceraldehyde 3-phosphate dehydrogenase (GAPDH), and peptidylprolyl isomerase A (PPIA)-decreased with increased storage time. Median values of each microarray probe intensity at log scale also decreased over time. After eight years of storage, probe intensity values were largely reduced to background intensity levels. Of 21,500 genes tested, 89% significantly decreased in signal intensity, with 13,551, 10,730, and 9925 genes detected within 5years, > 5 to <10years, and >10years of storage, respectively. We also examined the expression of two gender-specific genes (X inactivation-specific transcript, XIST and lysine-specific demethylase 5D, KDM5D) and seven gene sets representing the inflammatory, hypoxic, coagulative, and thyroidal pathways hypothesized to be related to CP risk to determine the effect of storage time on the detection of these biologically relevant genes. We found the gender-specific genes and CP-related gene sets detectable in all storage periods, but exhibited differential expression (between male vs. female or CP vs. control) only within the first six years of storage. We concluded that gene expression data quality deteriorates in unfrozen archived NBS over time and that differential gene expression profiling and analysis is recommended for those NBS samples collected and stored within six years at ambient temperature.
已证明未冻存的存档新生儿血斑(NBS)保留有足够的信使核糖核酸(mRNA)用于基因表达谱分析。然而,NBS样本在室温下的储存时间对基因表达数据质量的影响相对未知。在此,我们评估了从室温储存的NBS样本获得的定量实时聚合酶链反应(qRT-PCR)和微阵列数据中的mRNA表达,以确定储存时间对基因表达质量的影响。这些数据来自之前一项病例对照研究,该研究检测了53名脑瘫(CP)患儿和53名匹配对照的NBS。NBS样本在室温下的储存期为3至16年。我们发现所有储存期的NBS样本中RNA完整性数值持续较低(RIN=2.3±0.71)且28S/18S核糖体RNA比值约为0。在qRT-PCR和微阵列数据中,三个常见管家基因——β细胞骨架肌动蛋白(ACTB)、甘油醛-3-磷酸脱氢酶(GAPDH)和肽基脯氨酰异构酶A(PPIA)的表达均随储存时间增加而降低。每个微阵列探针强度对数标度的中位数也随时间下降。储存八年之后,探针强度值大幅降至背景强度水平。在检测的21500个基因中,89%的基因信号强度显著降低,在储存5年以内、>5至<10年以及>10年的样本中分别检测到13551个、10730个和9925个基因。我们还检测了两个性别特异性基因(X染色体失活特异性转录本,XIST和赖氨酸特异性去甲基化酶5D,KDM5D)以及代表炎症、缺氧、凝血和甲状腺途径的七个基因集(假设与CP风险相关)的表达,以确定储存时间对这些生物学相关基因检测的影响。我们发现性别特异性基因和CP相关基因集在所有储存期均可检测到,但仅在储存的前六年内表现出差异表达(男性与女性之间或CP与对照之间)。我们得出结论,未冻存的存档NBS中的基因表达数据质量会随时间下降,对于在室温下收集并储存六年以内的NBS样本,建议进行差异基因表达谱分析。