Identification of reference genes in blood before and after entering the plateau for SYBR green RT-qPCR studies
Author(s) -
Jun Xiao,
Xiaowei Li,
Juan Liu,
Fan Xiu,
Huifen Lei,
Cuiying Li
Publication year - 2017
Publication title -
peerj
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.927
H-Index - 70
ISSN - 2167-8359
DOI - 10.7717/peerj.3726
Subject(s) - reference genes , sdha , biology , gene expression , gene , housekeeping gene , real time polymerase chain reaction , computational biology , genetics , glyceraldehyde 3 phosphate dehydrogenase , gene expression profiling
Background Tibetans have lived at high altitudes for thousands of years, and they have unique physiological traits that enable them to tolerate this hypoxic environment. However, the genetic basis of these traits is still unknown. As a sensitive and highly efficient technique, RT-qPCR is widely used in gene expression analyses to provide insight into the molecular mechanisms underlying environmental changes. However, the quantitative analysis of gene expression in blood is limited by a shortage of stable reference genes for the normalization of mRNA levels. Thus, systematic approaches were used to identify potential reference genes. Results The expression levels of eight candidate human reference genes ( GAPDH , ACTB , 18S RNA , β 2-MG , PPIA , RPL13A , TBP and SDHA ) were assessed in blood from hypoxic environments. The expression stability of these selected reference genes was evaluated using the geNorm, NormFinder and BestKeeper programs. Interestingly, RPL13A was identified as the ideal reference gene for normalizing target gene expression in human blood before and after exposure to high-altitude conditions. Conclusion These results indicate that different reference genes should be selected for the normalization of gene expression in blood from different environmental settings.
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