Supplementary Information. HBx-upregulated lncrna UCA1 promotes cell growth and tumorigenesis
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1 Supplementary Information HBx-upregulated lncrna UCA1 promotes cell growth and tumorigenesis by recruiting EZH2 and repressing p27kip1/cdk2 signaling Jiao-Jiao Hu 1, Wei Song 1, Shao-Dan Zhang 1, Xiao-Hui Shen 1, Xue-Mei Qiu 1, Hua-Zhang Wu 1, Pi-Hai Gong 1, Sen Lu 3, Zhu-Jiang Zhao 1, Ming-Liang He 2 *, Hong Fan 1 * Table of contents Supplementary Figure... 2 Supplementary Table
2 Supplementary Figure Supplementary Fig. S1, related to Fig. 2. The expression levels of HBx and UCA1 in LO2 cells. (a) The HBx protein levels detected by western blot with the anti-his tag antibody. (b) The levels of UCA1 mrna in LO2-HBx stable cells measured by qrt-pcr. Supplementary Fig. S2, related to Fig. 3. The Role of UCA1 in cells proliferation. (a) The mrna expression of HBx and UCA1 were detected by conventional RT-PCR. Cell proliferation was measured by Cell Counting Kit-8 assays. (b) QSG-7701 were overexpressed with HBx. (c) HepG2 cells were transfected with UCA1-specific sirna. All data represent mean ± SD, n=3, *, P <0.05 by Student s t-test. 2
3 Supplementary Fig. S3, related to Fig. 4. The quantification of the western blot signals are analyzed for Figure 4c. All data represent mean ± SD, n=3, *, P <0.05 by Student s t-test. Supplementary Fig. S4, related to Fig. 5. The p27 protein levels detected by western blot with the anti-p27 antibody. 3
4 Supplementary Fig. S5, related to Fig. 6. The physical association of UCA1 and EZH2 elevating p27 3MeK27H3 level in promoters. (a) RIP assys were carried out without (left) or with (right) RNase treated. UCA1 were detected by conventional RT-PCR. (b) Before and after immunoprecipitation of CHIP, western blot experiments were carried. The results showed that EZH2 and H3K27me3 were efficiently immunoprecipitated from the cell lysates. The data are representative of two independent experiments. (c) The UCA1 expression level in cells nuleus were measured by qrt-pcr. (d) ChIP assys.cell lysates from LO2-HBx cells without and with UCA1 knockdown were applied for immunoprecipitation using anti-ezh2, H3K27me3, Histone H3 and IgG antibodies. Foxc1 promoter was quantified by qrt-pcr. The values indicate the mean ± SD. Statistically significant differences are reported for two independent experiments. (e) The levels of p27 mrna were detected by qrt-pcr in HepG2 cells transfected with indicated sirna, or 4
5 UCA1-expressing plasmids, respectively. Student t-test was conducted for statistic assays. At least two independent experiments were conducted. *, P <
6 Supplementary Fig. S6,related to Fig. 7. Images of tumors in the nude mice injected with the indicated hepatoma cells after 4-week inoculation. 6
7 Supplementary Fig. S7. A diagram of HBx-UCA1-p27 axis signaling. HBx activiates UCA1 expression, then UCA1 recruits EZH2 to p27 promoter and suppresses p27 expression. The reduced p27 protein level leads to high level active CDK2, that leads to G1/S transition and inhibition of apoptosis., activation; --, inhibition. 7
8 Supplementary Table 1 Supplementary Table. Oligonucleotide Sequences used in this study. Gene Sequence (5 to 3 ) products size (bp) ENST F:CTCCTTTGATTTGGCTGAC 124 R:GACCGAGACTCCATCCTG LOC F:TATCTTTAGGCGTGGTG 184 R:GGTATAAGGTTGGCACTA LOC F:CTCGGCTTCTTCCTCTGTGC 138 R:TCATCCATACACCCTTGTGACTT LOC F:GCCGAAGGACAAAGAGTGAA 285 R:CGCCAAATGGGAAGCAA KRT42P F: GCTCAGCAAGAAAGCATCGC 141 R: TCCTGGTGCTCCGTGTCG SPRR2C F: AGACTCCAGCAGGATCAATGTAA 178 R: AGACTCCAGCAGGATCAATGTAA CEACAMP10 F: TGTCGGCATCCTGATTGG 159 R: AGTGGGTCTTGCTCTTCGTG ENST F: TGCCTCATGGAGCTGTCGTA 163 R: TGCTATTGCTGGAGCGTAGA OR7E25P F: TCGCATGTATGGAAAGTC 193 R: TCGTTGAAGCAGGTAAGT HBx F: TTCTTCGTCTGCCGTTCC 201 R: TCGGTCGTTGACATTGCT HBx-97 F:GACGTCCTTTGTCTACGTCC 97 8
9 R:GAACGGCAGATGAAGAAGGG UCA1 F:CTCTCCATTGGGTTCACCATTC 254 R:GCGGCAGGTCTTAAGAGATGAG P27 F:CCGGCTAACTCTGAGGACAC 120 R:AGAAGAATCGTCGGTTGCAG P21 F:TGATTAGCAGCGGAACAAG 218 R:AACAGTCCAGGCCAGTATG EZH2 F:GAAGCAGGGACTGAAACGG 170 R:ATTGAGGCTTCAGCACCACT ACTB F:GTCATTCCAAATATGAGATGCGT 125 R:GCTATCACCTCCCCTGTGTG U6 F: CGCTTCGGCAGCACATATACTA 90 R: CGCTTCACGAATTTGCGTGTCA HOTAIR F: GGTAGAAAAAGCAACCACGAAGC 170 R: ACATAAACCTCTGTCTGTGAGTGCC GAPDH GCACCGTCAAGGCTGAGAAC 138 TGGTGAAGACGCCAGTGGA UCA1 clone F:CCCAAGCTTTGACATTCTTCTGGAC 1423 R: GGAATTCAATCAGGCATATTAGCTT CHIP p27 Pa F: TCTGGGTTAAGGCTGAGCGA 206 R: GAGGACCGCGAAGGTCG CHIP p27 Pb F: GCTCCTAGCGAGCTGCC 204 R: GGCTGGCCTCGGAGAAATTA CHIP p27 Pc F:TTTTAATTTCTCCGAGGCCAGC 207 9
10 R:GAGATCCATTGGTTGCGGCG CHIP p27 Pd F:TTCTTCGTCAGCCTCCCTTC 170 R: AGCCGCTCTCCAAACCTTG CHIP p27 Pe F: CTGGTCCCCTCTCCTCTCC 177 R: CGAACCCCTCTCGGAAGC CHIP p27 Pf F: GCTTCCGAGAGGGGTTCG 194 R: GGTTCCTGCAGGCCGAG CHIP p27 Pg F: GATGGACGCCAGGCAGG 204 R: CTGCCCTTCTCCACCTCTTG CHIP p27 Ph F: CCCCTAGAGGGCAAGTACGA 167 R: TTAGCCGGAGCCCCAATTAAA CHIP Foxc1 F:ACCCCTTGCCTTCATTTGG 218 R:AGCCCCTTCCCTCCCTTCT sirna sequence HBx-siRNA Sense: CUUGGACUCUCAGCAAUGUTT Antisense:ACAUUGCUGAGAGUCCAAGTT UCA1-siRNA1 Sense: GUUAAUCCAGGAGACAAAGATT Antisense:UCUUUGUCUCCUGGAUUAACTT UCA1-siRNA2 Sense: GGACAACAGUACACGCAUAdTdT Antisense:TATGCGTGTACTGTTGTCCdTdT EZH2-siRNA Sense: GAGGUUCAGACGAGCUGAUUU Antisense:AAAUCAGCUCGUCUGAACCUC 10
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Gene Forward Primer Reverse Primer GAPDH ATCATCCCTGCCTCTACTGG GTCAGGTCCACCACTGACAC SSB1 AACTTCAGTGAGCCAAACCC GTTCTCAGAGGCTGGAGAGG
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