Identification of Suitable Reference Genes for Gene Expression Studies in Tissues from Fructose-Fed Rats
2012
Аутори:
Đorđević, AnaVojnović-Milutinović, Danijela
Tanić, Nikola
Bursać, Biljana
Teofilović, Ana
Veličković, Nataša
Elaković, Ivana
Matić, Gordana
Тип документа:
Чланак у часопису (Објављена верзија)
,
© 2012 American Scientific Publishers
Метаподаци
Приказ свих података о документуАпстракт:
Selection of appropriate endogenous control for normalization in a specific experimental paradigm is a critical step in the quantification of gene expression. The aim of this study was to identify suitable reference gene(s) for simultaneous normalization of gene expression in liver and adipose tissue of control and fructose-fed male rats which is considered as model of metabolic syndrome. Using TaqMan Real Time RT-PCR, we carried out an extensive evaluation of five frequently used endogenous controls, b-actin, b2-microglobulin, 18S rRNA, hypoxanthine phosphoribosyl transferase 1 and TATA box binding protein, for their presumed stability of expression.
Expression stability was analyzed by GeNorm and NormFinder software packages, and by direct comparison of Ct values. Both, GeNorm and NormFinder identified 2-microglobulin in the liver, hypoxanthine phosphoribosyl transferase 1 in the adipose tissue and TATA box binding protein for comparative analysis of the two tissues as
most stable genes. The combination of b-actin and TATA box binding protein in the liver, hypoxanthine phosphoribosyl transferase 1 and TATA box binding protein in the adipose tissue and b-actin and TATA box binding protein for both tissues together appeared to be the most suitable combinations of reference genes for studying
alterations in gene expression in fructose-fed rats.
Кључне речи:
endogenous control; fructose diet; liver; Adipose tissue; rat; qRT-PCRИзвор:
Advanced Science Letters, 2012, 5, 2, 560-565(6)Финансирање / пројекти:
- Улога стероидних хормона у неуроендокриној адаптацији на стрес и патофизиологији метаболичког синдрома - молекуларни механизми и клиничке импликације (RS-MESTD-Integrated and Interdisciplinary Research (IIR or III)-41009)
URI
https://www.ingentaconnect.com/content/asp/asl/2012/00000005/00000002/art00019%3bjsessionid=4lrjbbnfmh61v.x-ic-live-03https://radar.ibiss.bg.ac.rs/handle/123456789/3463