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PMID: 12446457 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

ELL-associated factor 2 (EAF2), a functional homolog of EAF1 with alternative ELL binding properties.

Blood ·Vol. 101 ·No. 6 ·2003-03-15 ·Pages 2355-62

Simone F, Luo RT, Polak PE, Kaberlein JJ, Thirman MJ

Abstract

The (11;19)(q23;p13.1) translocation in acute leukemia results in the formation of an MLL-ELL fusion protein. ELL is an RNA polymerase II elongation factor that interacts with the recently identified EAF1 protein. To characterize the normal functions of ELL and its aberrant activities when fused to MLL, we isolated a second protein that interacts with ELL named EAF2 for ELL Associated Factor 2. EAF2 is highly homologous to EAF1, with 58% identity and 74% amino acid conservation. Using specific antibodies generated to EAF2, we coimmunoprecipitated ELL and EAF2 from multiple cell lines. Confocal microscopy revealed that endogenous EAF2 and ELL colocalized in a nuclear speckled pattern. Database comparisons with EAF2 identified a region with a high content of serine, aspartic acid, and glutamic acid residues that is conserved with EAF1 and exhibited amino acid similarity with several translocation partner proteins of MLL, including AF4 and ENL. We found that EAF2 and EAF1 both contain transcriptional activation domains within this region. Using retroviral bone marrow transduction, we observed that a heterologous fusion of EAF2 to MLL immortalized hematopoietic progenitor cells. In contrast to EAF1, EAF2 does not bind to the carboxy-terminus of ELL. We identified a protein-protein interaction domain within the amino-terminus of ELL that binds to both EAF1 and EAF2. This amino-terminal interaction domain is disrupted in the formation of the MLL-ELL fusion protein. Thus, MLL-ELL retains an interaction domain for EAF1 but not for EAF2. Taken together, these data suggest that MLL-ELL may disrupt the normal protein-protein interactions of ELL.

MeSH Terms
Amino Acid Sequence Animals Aspartic Acid/analysis Binding Sites Blotting, Northern Bone Marrow/metabolism Cell Nucleus/chemistry Cell Transformation, Neoplastic Conserved Sequence DNA-Binding Proteins/genetics Glutamic Acid/analysis HeLa Cells Hematopoietic Stem Cells/pathology Histone-Lysine N-Methyltransferase Humans Immunosorbent Techniques Leukemia, Myeloid, Acute/pathology Mice Molecular Sequence Data Myeloid-Lymphoid Leukemia Protein Oncogene Proteins, Fusion/chemistry,genetics,metabolism Peptide Fragments/metabolism Proto-Oncogenes Recombinant Fusion Proteins Retroviridae/genetics Sequence Homology Serine/analysis Transcription Factors/analysis,chemistry,genetics,metabolism Transcriptional Elongation Factors Transfection
Chemicals
DNA-Binding Proteins EAF1 protein, human EAF2 protein, human ELL2 protein, human KMT2A protein, human MLL-ELL fusion protein, human Oncogene Proteins, Fusion Peptide Fragments Recombinant Fusion Proteins Transcription Factors Transcriptional Elongation Factors Myeloid-Lymphoid Leukemia Protein Aspartic Acid Glutamic Acid Serine Histone-Lysine N-Methyltransferase Kmt2a protein, mouse
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Simone Federico
University of Chicago, Section of Hematology/Oncology, Chicago, IL 60637, USA.
Luo Roger T
Polak Paul E
Kaberlein Joseph J
Thirman Michael J
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
2003-03-15
Epub
2002-00-21
Pages
2355-62
Language
English
Region
United States
NLM ID
7603509
Subset
IM
Grants
NCI NIH HHS · CA14599 · United States
NCI NIH HHS · CA78431 · United States
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