Transcriptional expression of type-I interferon response genes and stability of housekeeping genes in the human endometrium and endometriosis

• Published in: Molecular human reproduction 2011-04, Vol.17 (3-4), p.243-254
• Main Authors: VESTERGAARD, Anna L, KNUDSEN, Ulla B, MUNK, Torben, ROSBACH, Hanne, MARTENSEN, Pia M
• Format: Article
• Language: English
• Subjects: Adult; Biological and medical sciences; Cell Line, Tumor; Embryology: invertebrates and vertebrates. Teratology; Endometriosis - genetics; Endometriosis - metabolism; Endometriosis - physiopathology; Endometrium - metabolism; Female; Fundamental and applied biological sciences. Psychology; Gene Expression Regulation; Humans; Interferon Type I - genetics; Interferon Type I - metabolism; Middle Aged
• ISSN: 1360-9947; 1460-2407
• DOI: 10.1093/molehr/gaq100

Endometriosis is a painful chronic female disease defined by the presence of endometrial tissue implants in ectopic (Ec) locations. The pathogenesis is much debated, and type-I interferons (IFNs) could be involved. The expression of genes of the type-I IFN response were profiled by a specific PCR array of RNA obtained from Ec and eutopic (Eu) endometrium collected from nine endometriosis patients and nine healthy control women. Transcriptional expression levels of selected IFN-regulated and housekeeping genes (HKGs) were investigated by real-time quantitative reverse transcriptase PCR (qRT-PCR). Stably expressed HKGs for valid normalization of transcriptional studies of endometrium and endometriosis have not yet been published. Here, seven HKGs were evaluated for stability using the GeNorm and NormFinder software. A normalization factor based on HMBS, TBP and YWHAZ expression was suitable for normalization of qRT-PCR studies of Eu versus Ec endometrium. In the endometrial cell lines HEC1A, HEC1B, Ishikawa and RL95-2, HMBS and HPRT1 were the most stably expressed. The IFN-specific PCR array indicated significantly different expression of the genes BST2, COL16A1, HOXB2 and ISG20 between the endometrial tissue types. However, by correctly normalized qRT-PCR, levels of BST2, COL16A1 and the highly type-I IFN-stimulated genes ISG12A and 6-16 displayed insignificant variations. Conversely, HOXB2 and ISG20 transcriptions were significantly reduced in endometriosis lesions compared with endometrium from endometriosis patients and healthy controls. In conclusion, appropriate HKGs for normalization of qRT-PCR studies of endometrium and endometriosis have been identified here. Abolished expression of ISG20 and HOX genes could be important in endometriosis.