TY - JOUR
T1 - Isolation and selection of suitable reference genes for real-time PCR analyses in the skeletal muscle of the fine flounder in response to nutritional status
T2 - Assessment and normalization of gene expression of growth-related genes
AU - Fuentes, Eduardo N.
AU - Safian, Diego
AU - Valdés, Juan Antonio
AU - Molina, Alfredo
N1 - Funding Information:
Acknowledgments We thank Juan Manuel Estrada for technical assistance at the Centro de Investigacion Marina de Quintay (CIMARQ, Chile); Dr. Neil I. Bower and Dr. Daniel J. Macqueen (University of St. Andrews, Scotland) for offering advice on the qPCRs assays; Dr. Jose Pulgar for statistical analysis advice (Universidad Andres Bello); and Ashley VanCott, BA (The University of Nevada, Reno, USA) for improving and correcting the English of the manuscript. This work was funded by FONDECYT N°1090416 grant to A Molina and Universidad Andres Bello grant DI-14-11/I to EN Fuentes.
PY - 2013/8
Y1 - 2013/8
N2 - In the present study, different reference genes were isolated, and their stability in the skeletal muscle of fine flounder subjected to different nutritional states was assessed using geNorm and NormFinder. The combinations between 18S and ActB; Fau and 18S; and Fau and Tubb were chosen as the most stable gene combinations in feeding, long-term fasting and refeeding, and short-term refeeding conditions, respectively. In all periods, ActB was identified as the single least stable gene. Subsequently, the expression of the myosin heavy chain (MYH) and the insulin-like growth factor-I receptor (IGF-IR) was assessed. A large variation in MYH and IGF-IR expression was found depending on the reference gene that was chosen for normalizing the expression of both genes. Using the most stable reference genes, mRNA levels of MYH decreased and IGF-IR increased during fasting, with both returning to basal levels during refeeding. However, the drop in mRNA levels for IGF-IR occurred during short-term refeeding, in contrast with the observed events in the expression of MYH, which occurred during long-term refeeding. The present study highlights the vast differences incurred when using unsuitable versus suitable reference genes for normalizing gene expression, pointing out that normalization without proper validation could result in a bias of gene expression.
AB - In the present study, different reference genes were isolated, and their stability in the skeletal muscle of fine flounder subjected to different nutritional states was assessed using geNorm and NormFinder. The combinations between 18S and ActB; Fau and 18S; and Fau and Tubb were chosen as the most stable gene combinations in feeding, long-term fasting and refeeding, and short-term refeeding conditions, respectively. In all periods, ActB was identified as the single least stable gene. Subsequently, the expression of the myosin heavy chain (MYH) and the insulin-like growth factor-I receptor (IGF-IR) was assessed. A large variation in MYH and IGF-IR expression was found depending on the reference gene that was chosen for normalizing the expression of both genes. Using the most stable reference genes, mRNA levels of MYH decreased and IGF-IR increased during fasting, with both returning to basal levels during refeeding. However, the drop in mRNA levels for IGF-IR occurred during short-term refeeding, in contrast with the observed events in the expression of MYH, which occurred during long-term refeeding. The present study highlights the vast differences incurred when using unsuitable versus suitable reference genes for normalizing gene expression, pointing out that normalization without proper validation could result in a bias of gene expression.
KW - Fish
KW - Growth-related genes
KW - Nutritional status
KW - Reference genes
KW - Skeletal muscle
UR - http://www.scopus.com/inward/record.url?scp=84879840576&partnerID=8YFLogxK
U2 - 10.1007/s10695-012-9739-5
DO - 10.1007/s10695-012-9739-5
M3 - Article
C2 - 23086610
AN - SCOPUS:84879840576
SN - 0920-1742
VL - 39
SP - 765
EP - 777
JO - Fish Physiology and Biochemistry
JF - Fish Physiology and Biochemistry
IS - 4
ER -