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. 2019 Oct 10;20(12):e48170. doi: 10.15252/embr.201948170

Figure 3. LINC00115 physically associates with miR‐200s.

Figure 3

  • 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), ***< 0.001, by two‐tailed t‐test. In (E and F), *< 0.05, **< 0.01, by one‐way ANOVA.