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. 2020 Feb 28;11(2):155. doi: 10.1038/s41419-020-2338-y

Fig. 5. LncRNA LDLRAD4-AS1 disrupts the stability of LDLRAD4 mRNA.

Fig. 5

a Expression levels of LDLRAD4 in LDLRAD4-AS1-overexpression cells using qRT-PCR analysis. b Expression levels of lncRNA LDLRAD4-AS1 in LDLRAD4-overexpression cells using qRT-PCR analysis. c Expression levels of LDLRAD4 in LDLRAD4-AS1-overexpression cells using western blotting. d Expression levels of LDLRAD4 in LDLRAD4-AS1-depleted cells using qRT-PCR analysis. e Expression levels of lncRNA LDLRAD4-AS1 in LDLRAD4-depleted cells using qRT-PCR analysis. f Expression levels of LDLRAD4 in LDLRAD4-AS1-depleted cells using western blotting. g RNA fluorescence in situ hybridization (FISH) showed that lncRNA LDLRAD4-AS1 and LDLRAD4 were both located in the nucleus in close proximity to each other. hk LncRNA LDLRAD4-AS1 overexpression disrupted stability of LDLRAD4 mRNA compared with the control group (hi), whereas the stability of LDLRAD4 mRNA was obviously increased after lncRNA LDLRAD4-AS1 knockdown compared with the control group (j, k). l All five truncated mutants and lncRNA LDLRAD4-AS1 full length are illustrated. m Forced expression of three truncated mutants (TM-549-5′, TM-1098-5′, and TM-1098-M) significantly downregulated the levels of LDLRAD4 mRNA as lncRNA LDLRAD4-AS1 full length did. For am, data were expressed as means ± SD in three independent experiments. *p < 0.05, **p < 0.01, ***p < 0.001.