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The effect of MSTN on the PI3K-AKT and ribosomal pathway. (A–C) Knockdown of MSTN expression resulted in a significant increase in mRNA expression level and protein expression level of majority differentially expressed proteins involved in PI3K-AKT and ribosomal pathway in GM, as well as a significant increase in the expression of key genes <t>AKT1,</t> RPS6, p-AKT1and p-RPS6 in the pathway. (D–F) The mRNA expression level and protein expression level of these proteins were also generally increased in DM3. These blots were cropped and original images were shown in and .
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The effect of MSTN on the PI3K-AKT and ribosomal pathway. (A–C) Knockdown of MSTN expression resulted in a significant increase in mRNA expression level and protein expression level of majority differentially expressed proteins involved in PI3K-AKT and ribosomal pathway in GM, as well as a significant increase in the expression of key genes <t>AKT1,</t> RPS6, p-AKT1and p-RPS6 in the pathway. (D–F) The mRNA expression level and protein expression level of these proteins were also generally increased in DM3. These blots were cropped and original images were shown in and .
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The effect of MSTN on the PI3K-AKT and ribosomal pathway. (A–C) Knockdown of MSTN expression resulted in a significant increase in mRNA expression level and protein expression level of majority differentially expressed proteins involved in PI3K-AKT and ribosomal pathway in GM, as well as a significant increase in the expression of key genes <t>AKT1,</t> RPS6, p-AKT1and p-RPS6 in the pathway. (D–F) The mRNA expression level and protein expression level of these proteins were also generally increased in DM3. These blots were cropped and original images were shown in and .
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The effect of MSTN on the PI3K-AKT and ribosomal pathway. (A–C) Knockdown of MSTN expression resulted in a significant increase in mRNA expression level and protein expression level of majority differentially expressed proteins involved in PI3K-AKT and ribosomal pathway in GM, as well as a significant increase in the expression of key genes AKT1, RPS6, p-AKT1and p-RPS6 in the pathway. (D–F) The mRNA expression level and protein expression level of these proteins were also generally increased in DM3. These blots were cropped and original images were shown in and .

Journal: Frontiers in Genetics

Article Title: Proteomic Studies on the Mechanism of Myostatin Regulating Cattle Skeletal Muscle Development

doi: 10.3389/fgene.2021.752129

Figure Lengend Snippet: The effect of MSTN on the PI3K-AKT and ribosomal pathway. (A–C) Knockdown of MSTN expression resulted in a significant increase in mRNA expression level and protein expression level of majority differentially expressed proteins involved in PI3K-AKT and ribosomal pathway in GM, as well as a significant increase in the expression of key genes AKT1, RPS6, p-AKT1and p-RPS6 in the pathway. (D–F) The mRNA expression level and protein expression level of these proteins were also generally increased in DM3. These blots were cropped and original images were shown in and .

Article Snippet: Several proteins were validated by western blot analysis using antibodies against the following proteins: Pax7 (1:100, DSHB, United States), MyoG (1:100, DSHB, United States), MyoD (1:100, DSHB, United States), MyHC (1:100, DSHB, United States), MSTN (1:100, Santa Cruz, United States), p-AKT1 (Ser-473) (1:200, Santa Cruz, Dallas, United States), COL1A1 (1:5,000, Abcam, United States), FAK (1:1,000, Abcam, United States), Rock1 (1:5,000, Abcam, United States), AKT1 (1:5,000, Abcam, United States), RhoA (1:1,000, NewEast, China), Rac1 (1:1,000, NewEast, China), LAMB1 (1:1,500, Sangon Biotech, China), MYL6 (1:500, Sangon Biotech, China), ACTN4 (1:1,000, Sangon Biotech, China), RPS6 (1:500, Sangon Biotech, China), p-FAK (Tyr-473) (1:500, Sangon Biotech, China), p-RPS6 (Ser-235/236) (1:500, Sangon Biotech, China), and reference gene Alpha-Tubulin (1:5,000, Abcam, United States).

Techniques: Knockdown, Expressing

Functional interaction network and a diagrammatic mode illustrate the regulatory mechanism of the MSTN gene on the focal adhesion, PI3K-AKT, and ribosomal pathways. (A) MSTN, FAK, AKT1, RPS6, and 55 Differentially expressed proteins were submitted to conduct blast searching against the existing databases in STRING 11 software. (B) “→” The activation of the process, “ -| ” the inhibition of the process, “– –” the presence of intermediate steps either unknown or omitted. Up-regulated differentially expressed proteins were marked with red font, while down-regulated differentially expressed proteins were marked with blue font.

Journal: Frontiers in Genetics

Article Title: Proteomic Studies on the Mechanism of Myostatin Regulating Cattle Skeletal Muscle Development

doi: 10.3389/fgene.2021.752129

Figure Lengend Snippet: Functional interaction network and a diagrammatic mode illustrate the regulatory mechanism of the MSTN gene on the focal adhesion, PI3K-AKT, and ribosomal pathways. (A) MSTN, FAK, AKT1, RPS6, and 55 Differentially expressed proteins were submitted to conduct blast searching against the existing databases in STRING 11 software. (B) “→” The activation of the process, “ -| ” the inhibition of the process, “– –” the presence of intermediate steps either unknown or omitted. Up-regulated differentially expressed proteins were marked with red font, while down-regulated differentially expressed proteins were marked with blue font.

Article Snippet: Several proteins were validated by western blot analysis using antibodies against the following proteins: Pax7 (1:100, DSHB, United States), MyoG (1:100, DSHB, United States), MyoD (1:100, DSHB, United States), MyHC (1:100, DSHB, United States), MSTN (1:100, Santa Cruz, United States), p-AKT1 (Ser-473) (1:200, Santa Cruz, Dallas, United States), COL1A1 (1:5,000, Abcam, United States), FAK (1:1,000, Abcam, United States), Rock1 (1:5,000, Abcam, United States), AKT1 (1:5,000, Abcam, United States), RhoA (1:1,000, NewEast, China), Rac1 (1:1,000, NewEast, China), LAMB1 (1:1,500, Sangon Biotech, China), MYL6 (1:500, Sangon Biotech, China), ACTN4 (1:1,000, Sangon Biotech, China), RPS6 (1:500, Sangon Biotech, China), p-FAK (Tyr-473) (1:500, Sangon Biotech, China), p-RPS6 (Ser-235/236) (1:500, Sangon Biotech, China), and reference gene Alpha-Tubulin (1:5,000, Abcam, United States).

Techniques: Functional Assay, Software, Activation Assay, Inhibition