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RACK7 ChIP-seq in pediatric glioblastomas cell lines.

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https://www.ncbi.nlm.nih.gov/sra/SRP223435
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We identified that RACK7 recognizes the histone H3.3G34R mutaion in vitro. In order to determine the interaction between RACK7 and H3.3G34R mutaion in cells, we used three pediatric glioblastoma (pGBM) cell lines. SJ-HGGx6c(R6) and SJ-HGGx42c(R42) have heterozygous G34R mutation, while SJ-HGGx39c(WT39) has wildtype H3F3A, which encodes H3.3, and we also corrected H3.3G34R in R6 and R42 cells to wildtype H3.3 by CRISPR/Cas9 mediated knock-in. Finally, we performed RACK7 ChIP-seq in these cell lines to explore the function of RACK7 and H3.3G34R mutation. Overall design: RACK7 ChIP-seq was carried out in three pGBM cell lines and two H3.3 CRISPR/Cas9 knock-in cell lines.
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2020-09-09
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