Chromatin-bound CRM1 recruits SET-Nup214 and NPM1c onto <i>HOX</i> clusters causing aberrant <i>HOX</i> expression in leukemia cells.

Abstract

We previously demonstrated that CRM1, a major nuclear export factor, accumulates at <i>Hox</i> cluster regions to recruit nucleoporin-fusion protein Nup98HoxA9, resulting in robust activation of <i>Hox</i> genes (Oka et al., 2016). However, whether this phenomenon is general to other leukemogenic proteins remains unknown. Here, we show that two other leukemogenic proteins, nucleoporin-fusion SET-Nup214 and the NPM1 mutant, NPM1c, which contains a nuclear export signal (NES) at its C-terminus and is one of the most frequent mutations in acute myeloid leukemia, are recruited to the <i>HOX</i> cluster region via chromatin-bound CRM1, leading to <i>HOX</i> gene activation in human leukemia cells. Furthermore, we demonstrate that this mechanism is highly sensitive to a CRM1 inhibitor in leukemia cell line. Together, these findings indicate that CRM1 acts as a key molecule that connects leukemogenic proteins to aberrant <i>HOX</i> gene regulation either via nucleoporin-CRM1 interaction (for SET-Nup214) or NES-CRM1 interaction (for NPM1c).