Too Issac H K, Ling Maurice H T
Department of Biological Sciences, National University of Singapore, Singapore 117543.
Department of Zoology, The University of Melbourne, Parkville, Victoria 3010, Australia.
ISRN Bioinform. 2011 Dec 28;2012:790452. doi: 10.5402/2012/790452. eCollection 2012.
Lung cancer is a common cancer, and expression profiling can provide an accurate indication to advance the medical intervention. However, this requires the availability of stably expressed genes as reference. Recent studies had shown that genes that are stably expressed in a tissue may not be stably expressed in other tissues suggesting the need to identify stably expressed genes in each tissue for use as reference genes. DNA microarray analysis has been used to identify those reference genes with low fluctuation. Fourteen datasets with different lung conditions were employed in our study. Coefficient of variance, followed by NormFinder, was used to identify stably expressed genes. Our results showed that classical reference genes such as GAPDH and HPRT1 were highly variable; thus, they are unsuitable as reference genes. Signal peptidase complex subunit 1 (SPCS1) and hydroxyacyl-CoA dehydrogenase beta subunit (HADHB), which are involved in fundamental biochemical processes, demonstrated high expression stability suggesting their suitability in human lung cell profiling.
肺癌是一种常见的癌症,表达谱分析可为推进医学干预提供准确指示。然而,这需要有稳定表达的基因作为参照。最近的研究表明,在一个组织中稳定表达的基因在其他组织中可能并不稳定表达,这表明需要在每个组织中鉴定稳定表达的基因作为参照基因。DNA微阵列分析已被用于鉴定那些波动较小的参照基因。我们的研究使用了14个具有不同肺部状况的数据集。采用变异系数,随后使用NormFinder来鉴定稳定表达的基因。我们的结果表明,诸如甘油醛-3-磷酸脱氢酶(GAPDH)和次黄嘌呤磷酸核糖转移酶1(HPRT1)等经典参照基因具有高度变异性;因此,它们不适宜作为参照基因。参与基本生化过程的信号肽酶复合体亚基1(SPCS1)和羟酰基辅酶A脱氢酶β亚基(HADHB)表现出高表达稳定性,表明它们适用于人肺细胞表达谱分析。