LMO2 activation by deacetylation is indispensable for hematopoiesis and T-ALL leukemogenesis

Author:

Morishima Tatsuya1ORCID,Krahl Ann-Christin1,Nasri Masoud1,Xu Yun1,Aghaallaei Narges1ORCID,Findik Betül1,Klimiankou Maksim1,Ritter Malte1,Hartmann Marcus D.2ORCID,Gloeckner Christian Johannes34ORCID,Stefanczyk Sylwia1ORCID,Lindner Christian1,Oswald Benedikt1,Bernhard Regine1,Hähnel Karin1,Hermanutz-Klein Ursula1,Ebinger Martin5,Handgretinger Rupert5,Casadei Nicolas6ORCID,Welte Karl5,Andre Maya57,Müller Patrick18ORCID,Bajoghli Baubak1ORCID,Skokowa Julia1ORCID

Affiliation:

1. Department of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tübingen, Germany;

2. Department of Protein Evolution, Max Planck Institute for Developmental Biology, Tübingen, Germany;

3. German Center for Neurodegenerative Diseases, Tübingen, Germany;

4. Center for Ophthalmology, Institute for Ophthalmic Research, University Hospital Tübingen, Tübingen, Germany;

5. University Children's Hospital Tübingen, Tübingen, Germany;

6. Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen, Tübingen, Germany;

7. Department of Pediatric Intensive Care, University of Basel Children’s Hospital, Basel, Switzerland; and

8. Friedrich Miescher Laboratory of the Max Planck Society, Tübingen, Germany

Abstract

Key Points LMO2 is deacetylated by the NAMPT/SIRT2 pathway. LMO2 deacetylation is essential for LIM domain binding 1 binding and TAL1 complex activation during hematopoiesis and T-ALL leukemogenesis.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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