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Data · dataset · 2026

<p>MARCHF5 KO leads to the stabilization of NOXA protein but not mRNA.</p>

Listed in UCL Research Data Repository

<p>A. Western blot for MCL1 and NOXA in wildtype or <i>MARCHF5</i> KO BC-3 or BCBL-1 iCas9 cells after 6 days of editing.

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B. Quantification of Western blot in panel A normalized to total protein stain and gAAVS1. C. qRT-PCR of <i>NOXA</i> mRNA in wildtype or <i>MARCHF5</i> KO BC-3 or BCBL-1 iCas9 cells after 6 days of editing.

D. BCBL-1 iCas9 g<i>AAVS1</i> or <i>MARCHF5</i> g3 were first Dox treated for 9 days to induce editing. Cells were then treated with either DMSO of 1.25 μM MG132 for 4 h before harvesting for Western blotting. E. Quantification of Western blots in panel D normalized to total protein stain and <i>gAAVS1</i>.

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F. Day 9 Dox-treated BCBL-1 iCas9 g<i>AAVS1</i> or <i>MARCHF5</i> g3 cells were treated with DMSO, 0.1 μM, or 0.25 μM of the MCL1 inhibitor S63845 for 2 days. Cell viability was measured with CellTiter-Glo 2.0 kit and expressed relative to gAAVS1. G. Reciprocal co-immunoprecipitation (co-IP) of the endogenous MARCHF5-NOXA complex in BC-3 cells.

Statistical differences were calculated using two-way ANOVA with Dunnett’s multiple comparison post-hoc test or unpaired t test as noted. Adjusted <i>p</i> values reflect post-hoc comparisons between each gRNA to gAAVS1 unless specifically noted. Error bars, standard error of the mean.</p>

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UCL Research Data Repositoryoai:figshare.com:article/3404914412 d agoJSON v1
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