A 2A peptide-based double-promoter expression vector that mediated the expression of four fluorescent proteins was constructed and transfected into primary porcine fetal fibroblasts.
Nevertheless, DNP mediated the expression of Rho family GTPase and induced cancer metastasis.
As shown in Figure 3B, the 5'-UTRs of KOG1 and GCN2 mediated the expression of the second cistron.
DNP mediated the expression of phosphorylated GTPase, ferritin, LYRIC, and RNA polymerase, and it decreased the expression of phosphorylated torsin-1A protein 1.
Both GmNPR1 proteins complemented the lost NPR1 function of the Arabidopsis npr1-1 mutand and mediated the expression of PR-1 and BGL2 following INA treatment and infection, respectively.
We therefore hypothesized that PGC-1β mediated the expression of TNF-α, IL-6, IL-8, MMP-3, MMP-13 and RANKL through ERK, p38 and NF-κB.
(C) PGC-1β mediated the expression of proinflammatory cytokines and apoptosis through extracellular signal-regulated kinase (ERK), p38 and NF-κB in RA-FLS.
The 3′ UTR is the site bound by miRNAs, suggesting the possibility that miRNAs may directly mediate the expression of PD-L1.
Furthermore, molecular characterization of OsSND2 suggested that it functions as a master regulator to directly mediate the expression of other MYBs and facilitate cellulose biosynthesis.
Therefore, a pathway that mediates the expression of PhaNPR1 but not downstream of PhaNPR1 may be important to defense against CymMV in P. aphrodite.
However, the DcuS/DcuR TCS could not produce a signal strong enough to mediate the expression of the gfp gene responding fumarate concentration.
