Danesh Moazed

Danesh Moazed, Ph.D.

Professor of Cell Biology (HMS)
HHMI Investigator
SGM 402B

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

Coupling of double-stranded RNA synthesis and siRNA generation in fission yeast RNAi.
Authors: Authors: Colmenares SU, Buker SM, Buhler M, Dlakic M, Moazed D.
Mol Cell
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Mek1 kinase is regulated to suppress double-strand break repair between sister chromatids during budding yeast meiosis.
Authors: Authors: Niu H, Li X, Job E, Park C, Moazed D, Gygi SP, Hollingsworth NM.
Mol Cell Biol
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Acetylated histone tail peptides induce structural rearrangements in the RSC chromatin remodeling complex.
Authors: Authors: Skiniotis G, Moazed D, Walz T.
J Biol Chem
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RNAi-dependent and -independent RNA turnover mechanisms contribute to heterochromatic gene silencing.
Authors: Authors: Bühler M, Haas W, Gygi SP, Moazed D.
Cell
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S. pombe LSD1 homologs regulate heterochromatin propagation and euchromatic gene transcription.
Authors: Authors: Lan F, Zaratiegui M, Villén J, Vaughn MW, Verdel A, Huarte M, Shi Y, Gygi SP, Moazed D, Martienssen RA, Shi Y.
Mol Cell
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Two different Argonaute complexes are required for siRNA generation and heterochromatin assembly in fission yeast.
Authors: Authors: Buker SM, Iida T, Bühler M, Villén J, Gygi SP, Nakayama J, Moazed D.
Nat Struct Mol Biol
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Centromere assembly and propagation.
Authors: Authors: Morris CA, Moazed D.
Cell
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Inhibition of homologous recombination by a cohesin-associated clamp complex recruited to the rDNA recombination enhancer.
Authors: Authors: Huang J, Brito IL, Villén J, Gygi SP, Amon A, Moazed D.
Genes Dev
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New alleles of SIR2 define cell-cycle-specific silencing functions.
Authors: Authors: Matecic M, Martins-Taylor K, Hickman M, Tanny J, Moazed D, Holmes SG.
Genetics
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Tethering RITS to a nascent transcript initiates RNAi- and heterochromatin-dependent gene silencing.
Authors: Authors: Bühler M, Verdel A, Moazed D.
Cell
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