-
A
The prediction for miR‐200 binding sites in the LINC00115 transcript sequence.
-
B, C
MS2‐RIP followed by qRT–PCR analysis of endogenous microRNA association with LINC00115. 12XMS2 empty vector, LINC00115‐12XMS2, or LINC00115‐mut‐12XMS2 with Flag‐tagged MS2 was co‐transfected into 1123 GSCs.
-
D
Schematics of the predicted binding sites of miR‐200s on LINC00115 and LINC00115 mutants.
-
E
RNA pull‐down and qRT–PCR assays of LINC00115 binding with miR‐200s. GSC1123 cell lysates were incubated with biotin‐labeled LINC00115.
-
F
Luciferase activity analysis of 1123 GSCs co‐transfected with miR‐200s and luciferase reporters containing LINC00115 WT, mutant, or empty vector (EV).
Data information: In (C, E, and F), data are representative of three independent experiments. Error bars, ± SD. In (C), ***
P < 0.001, by two‐tailed
t‐test. In (E and F), *
P < 0.05, **
P < 0.01, by one‐way ANOVA.