Figure 4.
PIM inhibition results in pre-rRNA processing defects. (A) Schematic showing pre-rRNA isoforms and positions of internal transcribed spacer (ITS) 1 (orange vertical bar) and 2 (yellow vertical bar) probes. Mature rRNA sequences within precursors are depicted as blue rectangular boxes, and spacers are depicted as black lines. Adapted from Tafforeau et al29 with permission. (B) Northern blot analysis for AZD1208-treated MOLM-16 and EOL-1 cells using ITS1 (left) and ITS2 (right) probes. Autoradiograms showing ITS1 probe hybridization are presented at 2 different exposures (top and bottom panels) to permit optimal visualization of all rRNA intermediates. ∗aberrant 18S-E intermediate. The 18S rRNA abundance was analyzed by methylene blue staining of northern blot membranes.

PIM inhibition results in pre-rRNA processing defects. (A) Schematic showing pre-rRNA isoforms and positions of internal transcribed spacer (ITS) 1 (orange vertical bar) and 2 (yellow vertical bar) probes. Mature rRNA sequences within precursors are depicted as blue rectangular boxes, and spacers are depicted as black lines. Adapted from Tafforeau et al29 with permission. (B) Northern blot analysis for AZD1208-treated MOLM-16 and EOL-1 cells using ITS1 (left) and ITS2 (right) probes. Autoradiograms showing ITS1 probe hybridization are presented at 2 different exposures (top and bottom panels) to permit optimal visualization of all rRNA intermediates. ∗aberrant 18S-E intermediate. The 18S rRNA abundance was analyzed by methylene blue staining of northern blot membranes.

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