| Literature DB >> 25282333 |
Alyson A Lokken1, Nicholas J Achille2, Ming-Jin Chang3, Jeffrey J Lin3, Aravinda Kuntimaddi4, Benjamin I Leach4, Bhavna Malik1, Jacqueline B Nesbit3, Shubin Zhang2, John H Bushweller4, Nancy J Zeleznik-Le5, Charles S Hemenway6.
Abstract
Acute leukemias caused by translocations of the MLL gene at chromosome 11 band q23 (11q23) are characterized by a unique gene expression profile. More recently, data from several laboratories indicate that the most commonly encountered MLL fusion proteins, MLLT1, MLLT3, and AFF1 are found within a molecular complex that facilitates the elongation phase of mRNA transcription. Mutational analyses suggest that interaction between the MLLT1/3 proteins and AFF family proteins are required for experimental transformation of hematopoietic progenitor cells (HPCs). Here, we define a specific pairing of two amino acids that creates a salt bridge between MLLT1/3 and AFF proteins that is critically important for MLL-mediated transformation of HPCs. Our findings, coupled with the newly defined structure of MLLT3 in complex with AFF1, should facilitate the development of small molecules that block this amino acid interaction and interfere with the activity of the most common MLL oncoproteins.Entities:
Keywords: Leukemic transformation; Mutation complementation; Oncoproteins; Protein binding
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Year: 2014 PMID: 25282333 PMCID: PMC4253547 DOI: 10.1016/j.leukres.2014.08.010
Source DB: PubMed Journal: Leuk Res ISSN: 0145-2126 Impact factor: 3.156