Danesh Moazed

Danesh Moazed, Ph.D.

Professor of Cell Biology (HMS)
HHMI Investigator

Danesh Moazed, Ph.D., is a Professor and HHMI Investigator in the Department of Cell Biology at Harvard Medical School.  He is a member of the Harvard Biophysics Program and the Harvard Initiative for RNA Medicine (HIRM). He received his undergraduate and Ph.D. degrees from the University of California in Santa Cruz and performed postdoctoral studies at the University of California in San Francisco.

The Moazed lab studies how genes are silenced and how silencing is epigenetically inherited across generations.  The lab’s interests revolve around diverse pathways of heterochromatin-mediated gene silencing in yeast and mammalian cells.  Work in budding yeast focuses on the structure and function of a diverged and relatively simple form of heterochromatin, which requires only three Silent information regulator (“Sir”) proteins that form a histone deacetylase and chromatin-binding complex.  Work in fission yeast focuses on a conserved example of heterochromatin that requires the nuclear RNA interference (RNAi) machinery, other RNA processing pathways, Heterochromatin protein 1 (HP1) homologs, and histone-modifying enzymes.  In mammalian cells, the work is focused on HP1-mediated and other heterochromatin formation pathways.  The lab uses approaches ranging from genetics and genomics, biochemical purification and reconstitution, and structural biology for their studies.  Ultimately, the lab seeks to understand the conserved fundamental principles that govern the assembly, function, and epigenetic propagation of heterochromatin.

Harvard Medical School

Dept. of Cell Biology, SGM 402B

240 Longwood Avenue

Boston, MA 02115

Lab telephone: 617-432-1258

Exit from mitosis is triggered by Tem1-dependent release of the protein phosphatase Cdc14 from nucleolar RENT complex.
Authors: Authors: Shou W, Seol JH, Shevchenko A, Baskerville C, Moazed D, Chen ZW, Jang J, Shevchenko A, Charbonneau H, Deshaies RJ.
Cell
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Net1, a Sir2-associated nucleolar protein required for rDNA silencing and nucleolar integrity.
Authors: Authors: Straight AF, Shou W, Dowd GJ, Turck CW, Deshaies RJ, Johnson AD, Moazed D.
Cell
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Nucleotides in 16S rRNA protected by the association of 30S and 50S ribosomal subunits.
Authors: Authors: Merryman C, Moazed D, McWhirter J, Noller HF.
J Mol Biol
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Nucleotides in 23S rRNA protected by the association of 30S and 50S ribosomal subunits.
Authors: Authors: Merryman C, Moazed D, Daubresse G, Noller HF.
J Mol Biol
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Silent information regulator protein complexes in Saccharomyces cerevisiae: a SIR2/SIR4 complex and evidence for a regulatory domain in SIR4 that inhibits its interaction with SIR3.
Authors: Authors: Moazed D, Kistler A, Axelrod A, Rine J, Johnson AD.
Proc Natl Acad Sci U S A
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A deubiquitinating enzyme interacts with SIR4 and regulates silencing in S. cerevisiae.
Authors: Authors: Moazed D, Johnson D.
Cell
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Specific protection of 16 S rRNA by translational initiation factors.
Authors: Authors: Moazed D, Samaha RR, Gualerzi C, Noller HF.
J Mol Biol
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Maintenance of the engrailed expression pattern by Polycomb group genes in Drosophila.
Authors: Authors: Moazed D, O'Farrell PH.
Development
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Interaction of antibiotics with A- and P-site-specific bases in 16S ribosomal RNA.
Authors: Authors: Woodcock J, Moazed D, Cannon M, Davies J, Noller HF.
EMBO J
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Sites of interaction of the CCA end of peptidyl-tRNA with 23S rRNA.
Authors: Authors: Moazed D, Noller HF.
Proc Natl Acad Sci U S A
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