Comparison between Let-7a and U6 as an internal reference for RT-qPCR of miRNAs in rat cartilage
10.7652/jdyxb201704006
- VernacularTitle:U6和let-7a作为定量检测miRNAs的内参在大鼠软骨中稳定性的比较
- Author:
Lin YI
;
Hua GUO
;
Dongxian GUO
;
Zixin MIN
;
Ying YUAN
;
Yitong ZHAO
;
Yan HAN
;
Nannan ZHONG
;
Jian SUN
- Keywords:
cartilage;
internal reference;
RT-qPCR;
U6;
Let-7a;
microRNAs (miRNAs)
- From:
Journal of Xi'an Jiaotong University(Medical Sciences)
2017;38(4):497-501,535
- CountryChina
- Language:Chinese
-
Abstract:
Objective To evaluate the stability of U6 and let-7a as internal reference genes of miRNAs in RTqPCR by using femoral head samples of cartilage tissue from inbred DA rats.Methods Total RNA was extracted from femoral head cartilage tissues of female DA rats at three different time points,i.e.at birth (D0),ablactation (D21) and maturation (D42).The expressions of different miRNAs (miR-1,-25,-26a,-140,-146a,-150,-181a,-195,-223 and-337) were detected by RT-qPCR using U6 or let-7a as the internal reference.The two sets of miR expression were compared with the results from Solexa sequencing in our pioneer work to evaluate the stability of the two internal references.Results The relative values of U6 (P =0.045) and let-7a (P =0.021 5) revealed significant difference in the D42 sample.Both in U6 and let-7a systems,miR-26a,-140,-223,and-337 showed a similar tendency in expression and quantification but miR-1 and-146a did not have significant differences.miR-25,-150,-181a and-195 differed significantly (P＜0.05).Comparison of absolute quantification results between the two generations' sequencing showed that let-7a is more stable than U6.Conclusion Let-7a is more suitable to be used as the internal reference gene in RT-qPCR for miRNAs in cartilage tissue.
