Chromosomal rearrangements resulting in alteration of gene expression are a major cause of hematological malignancies. This grant application is focused on the characterization of the molecular functions and biochemical properties of the MLL family of proteins and its chimeras in the hope of advancing our understanding of the molecular mechanisms of rearrangement-based leukemia. Our studies during the past five years have considerably expanded our molecular understanding of the role of MLL1 and one of its translocation partners, the ELL protein. We and others have identified MLL, MLL-related proteins and their complexes as histone H3 lysine 4 (H3K4) methylases. Through our biochemical and genetic screens, we have also identified the molecular machinery required for the proper enzymatic activity of the H3K4 methylases. We have also demonstrated that the ELL protein, one of the MLL1 partners in leukemia, is a bona fide RNA polymerase II elongation factor regulating the transcriptional properties of the elongating form of RNA polymerase II. These studies have helped to create the paradigm that posttranslational modifications of chromatin by methylation and transcriptional elongation control participate in the etiology of leukemia. Building on these discoveries, the goals of this proposal are to characterize the gene targets of the mammalian H3K4 methylases and to understand the molecular mechanism of translocation-based leukemia via MLL-chimeras. These goals will be aggressively pursued via two specific aims.
Specific Aim 1 is focused on identifying the gene targets of the six mammalian H3K4 methylases and to define how these methylases acquire their gene target specificity and understand the biological significance of H3K4 methylation at such sites.
Specific Aim 2 is focused on the biochemical isolation of several of the MLL-translocation chimeras and on defining their molecular composition in the hope of identifying a molecular commonality among the chimeras, which may result in the pathogenesis of a leukemic phenotype. We will take advantage of a variety of biochemical, molecular and genetic tools to address the aims proposed in this application. The proposed studies should (i) have a fundamental impact on our understanding of how MLL translocations result in the pathogenesis of hematological malignancies;and (ii) be instrumental for our understanding of the diverse roles that the mammalian H3K4 methylase machinery plays during development and differentiation. The information provided by these studies have the potential of some day proving helpful to investigators attempting to design rational approaches for the treatment of certain human malignancies using target specific therapeutics.

Public Health Relevance

Relevance: The focus of this application is on a group of proteins (MLL1-4 and Set1A/B) that regulate the posttranslational modification of the chromatin of living cells by methylation. This modification can alter cell growth, division, and differentiation properties. Importantly, one of these genes, the MLL1 is found in translocation-based leukemia. Therefore, detailed knowledge of the molecular functions of MLL and its family members will be critical for the detection, diagnosis and treatment of human leukemia.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA150265-04
Application #
8403710
Study Section
Molecular Genetics C Study Section (MGC)
Program Officer
Mufson, R Allan
Project Start
2010-03-09
Project End
2014-12-31
Budget Start
2013-01-01
Budget End
2013-12-31
Support Year
4
Fiscal Year
2013
Total Cost
$437,606
Indirect Cost
$162,382
Name
Stowers Institute for Medical Research
Department
Type
DUNS #
614653652
City
Kansas City
State
MO
Country
United States
Zip Code
64110
Smith, Edwin; Shilatifard, Ali (2014) Enhancer biology and enhanceropathies. Nat Struct Mol Biol 21:210-9
Herz, Hans-Martin; Hu, Deqing; Shilatifard, Ali (2014) Enhancer malfunction in cancer. Mol Cell 53:859-66
Smith, Edwin; Shilatifard, Ali (2013) Transcriptional elongation checkpoint control in development and disease. Genes Dev 27:1079-88
Rickels, Ryan; Shilatifard, Ali (2013) A histone modifier's ill-gotten copy gains. Cell 154:477-9
Hu, Deqing; Gao, Xin; Morgan, Marc A et al. (2013) The MLL3/MLL4 branches of the COMPASS family function as major histone H3K4 monomethylases at enhancers. Mol Cell Biol 33:4745-54
Hu, Deqing; Smith, Edwin R; Garruss, Alexander S et al. (2013) The little elongation complex functions at initiation and elongation phases of snRNA gene transcription. Mol Cell 51:493-505
Lin, Chengqi; Garruss, Alexander S; Luo, Zhuojuan et al. (2013) The RNA Pol II elongation factor Ell3 marks enhancers in ES cells and primes future gene activation. Cell 152:144-56
Hu, Deqing; Garruss, Alexander S; Gao, Xin et al. (2013) The Mll2 branch of the COMPASS family regulates bivalent promoters in mouse embryonic stem cells. Nat Struct Mol Biol 20:1093-7
Luo, Zhuojuan; Lin, Chengqi; Guest, Erin et al. (2012) The super elongation complex family of RNA polymerase II elongation factors: gene target specificity and transcriptional output. Mol Cell Biol 32:2608-17
Herz, Hans-Martin; Mohan, Man; Garrett, Alexander S et al. (2012) Polycomb repressive complex 2-dependent and -independent functions of Jarid2 in transcriptional regulation in Drosophila. Mol Cell Biol 32:1683-93

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