Interaction between the homeodomain protein HOXC13 and ETS family transcription factor PU.1 and its implication in the differentiation of murine erythroleukemia cells

• Published in: Experimental cell research Vol. 314; no. 4; pp. 847 - 858
• Main Authors: Yamada, Toshiyuki, Shimizu, Takeshi, Suzuki, Mitsuhiro, Kihara-Negishi, Fumiko, Nanashima, Naoki, Sakurai, Takuya, Fan, Yang, Akita, Miki, Oikawa, Tsuneyuki, Tsuchida, Shigeki
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 15.02.2008; Elsevier BV
• Subjects: Animals; Cell Differentiation; Cell Line, Tumor; Cells; Down-Regulation; Erythroid differentiation; Erythropoiesis; Gene expression; Genetic research; Genetics; Homeodomain Proteins - chemistry; Homeodomain Proteins - metabolism; HOXC13; Humans; Leukemia, Erythroblastic, Acute - metabolism; Mice; Murine erythroleukemia cells; Protein Structure, Tertiary; Proteins; Proto-Oncogene Proteins - antagonists & inhibitors; Proto-Oncogene Proteins - chemistry; Proto-Oncogene Proteins - metabolism; PU.1; Ribonucleic acid; RNA; Trans-Activators - antagonists & inhibitors; Trans-Activators - chemistry; Trans-Activators - metabolism; β-globin; β-globin; Murine erythroleukemia cells; HOXC13; Erythroid differentiation; PU.1
• ISSN: 0014-4827; 1090-2422
• DOI: 10.1016/j.yexcr.2007.11.005

Some of homeodomain proteins and the ETS family of transcription factors are involved in hematopoiesis. RT-PCR analysis revealed that the HOXC13 and PU.1 genes were expressed in murine erythroleukemia (MEL) cells and their levels decreased during DMSO-induced differentiation into erythroid cells. HOXC13 bound to the ETS domain of PU.1 through a region encompassing the C-terminal part of the homeodomain and the most C-terminal region and enhanced the transcriptional activity of PU.1. Enforced expression of HOXC13 in MEL cells resulted in the suppression of β-globin gene expression. In MEL cells overexpressing HOXC13 and PU.1, which also inhibits the differentiation of MEL cells, no synergistic effect on the suppression of β-globin gene expression was observed. However, in the presence of DMSO, the expression levels of the β-globin gene in the cells overexpressing HOXC13 and PU.1 were, unexpectedly, higher than those in the cells overexpressing PU.1 alone. The levels of PU.1 protein were markedly decreased despite that the levels of mRNA were preserved in the cells overexpressing PU.1 and HOXC13. It was, thus, suggested that although HOXC13 negatively regulates the differentiation of MEL cells into erythroid cells, it antagonizes PU.1 possibly by down-regulation of PU.1 protein in the presence of a differentiation stimulus.