Title : miR-16 controls myoblast proliferation and apoptosis through directly suppressing Bcl2 and FOXO1 activities.

Pub. Date : 2017 Jun

PMID : 28258011






7 Functional Relationships(s)
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1 miR-16 controls myoblast proliferation and apoptosis through directly suppressing Bcl2 and FOXO1 activities. mir-16 forkhead box O1 Gallus gallus
2 Here, we reported that miR-16 inhibited myoblast proliferation and promoted myoblast apoptosis by directly targeting Bcl2 and FOXO1. mir-16 forkhead box O1 Gallus gallus
3 Bioinformatic and biochemical analyses revealed Bcl2 and FOXO1 as direct targets of miR-16. mir-16 forkhead box O1 Gallus gallus
4 Consist to the effect of miR-16 on myogenesis, specific inhibition of Bcl2 or FOXO1 significantly suppressed myoblast proliferation and induced myoblast apoptosis, indicating that both Bcl2 and FOXO1 contributed to miR-16 regulatory function in myogenesis. mir-16 forkhead box O1 Gallus gallus
5 Consist to the effect of miR-16 on myogenesis, specific inhibition of Bcl2 or FOXO1 significantly suppressed myoblast proliferation and induced myoblast apoptosis, indicating that both Bcl2 and FOXO1 contributed to miR-16 regulatory function in myogenesis. mir-16 forkhead box O1 Gallus gallus
6 Interestingly, FOXO1, as the core target, mediated multiple growth-related pathways induced by miR-16 such as PI3K-AKT-MAPK and PI3K-AKT-mTOR. mir-16 forkhead box O1 Gallus gallus
7 These findings have provided a novel mechanism whereby miR-16 represses Bcl2 and FOXO1 expression to maintain myoblast growth and skeletal muscle mass. mir-16 forkhead box O1 Gallus gallus