Genetic analysis of Ikaros target genes and tumor suppressor function in BCR-ABL1+ pre–B ALL

Author:

Schjerven Hilde1ORCID,Ayongaba Etapong F.12ORCID,Aghajanirefah Ali1,McLaughlin Jami3,Cheng Donghui4,Geng Huimin1,Boyd Joseph R.5ORCID,Eggesbø Linn M.12,Lindeman Ida12ORCID,Heath Jessica L.67ORCID,Park Eugene1ORCID,Witte Owen N.348ORCID,Smale Stephen T.348,Frietze Seth9,Müschen Markus10

Affiliation:

1. Department of Laboratory Medicine, University of California, San Francisco, CA 94143

2. Department of Biosciences, University of Oslo, 0316 Oslo, Norway

3. Department of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, CA 90095

4. Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, University of California, Los Angeles, CA 90095

5. Department of Biochemistry and University of Vermont Cancer Center, University of Vermont, Burlington, VT 05405

6. Department of Pediatrics, University of Vermont, Burlington, VT 05405

7. Department of Biochemistry, University of Vermont, Burlington, VT 05405

8. Molecular Biology Institute, University of California, Los Angeles, CA 90095

9. Department of Medical Laboratory and Radiation Science, University of Vermont, Burlington, VT 05405

10. Department of Systems Biology, Beckman Research Institute and City of Hope Comprehensive Cancer Center, Pasadena, CA 91016

Abstract

Inactivation of the tumor suppressor gene encoding the transcriptional regulator Ikaros (IKZF1) is a hallmark of BCR-ABL1+ precursor B cell acute lymphoblastic leukemia (pre–B ALL). However, the mechanisms by which Ikaros functions as a tumor suppressor in pre–B ALL remain poorly understood. Here, we analyzed a mouse model of BCR-ABL1+ pre–B ALL together with a new model of inducible expression of wild-type Ikaros in IKZF1 mutant human BCR-ABL1+ pre–B ALL. We performed integrated genome-wide chromatin and expression analyses and identified Ikaros target genes in mouse and human BCR-ABL1+ pre–B ALL, revealing novel conserved gene pathways associated with Ikaros tumor suppressor function. Notably, genetic depletion of different Ikaros targets, including CTNND1 and the early hematopoietic cell surface marker CD34, resulted in reduced leukemic growth. Our results suggest that Ikaros mediates tumor suppressor function by enforcing proper developmental stage–specific expression of multiple genes through chromatin compaction at its target genes.

Funder

National Institutes of Health

American Cancer Society

Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research

NCI

Arthritis National Research Foundation

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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