Human MAF1 targets and represses active RNA polymerase III genes by preventing recruitment rather than inducing long-term transcriptional arrest

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 2.
Figure 2.

Pol III recruitment is controlled genome-wide by MAF1 in an mTORC1-dependent manner. (A) Depletion of MAF1 by RNAi. Immunoblots of IMR90hTert cells that were not transfected (NT) or were transfected with a control (nontarget) siRNA or with two MAF1-specific siRNAs (#1 and #2), and serum-starved for 8 h. (B) Violin plots showing distributions of Pol III ChIP-seq scores from IMR90hTert cells transfected as described in A. Nonoccupied genes are in gray. The median is in each case represented by a white asterisk. Data were analyzed with Wilcoxon pairs tests. (***) P < 0.001. (C) MA-plot comparing Pol III occupancy scores in MAF1 knockdown cells (mean of #1 and #2 MAF1 siRNAs) versus the control (#NEG siRNA). Gray dots left of the dotted lines (indicating the cutoff threshold score) represent nonoccupied genes. The horizontal line indicates the zero-fold change. Red dots indicate stable genes as defined in Pol III ChIP-seq experiments.

This Article

  1. Genome Res. 26: 624-635

Preprint Server