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

Binding of tRNA to the ribosomal A and P sites protects two distinct sets of nucleotides in 16 S rRNA.
Authors: Authors: Moazed D, Noller HF.
J Mol Biol
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Intermediate states in the movement of transfer RNA in the ribosome.
Authors: Authors: Moazed D, Noller HF.
Nature
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Interaction of tRNA with 23S rRNA in the ribosomal A, P, and E sites.
Authors: Authors: Moazed D, Noller HF.
Cell
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Mutations in 16S ribosomal RNA disrupt antibiotic--RNA interactions.
Authors: Authors: De Stasio EA, Moazed D, Noller HF, Dahlberg AE.
EMBO J
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Interaction of elongation factors EF-G and EF-Tu with a conserved loop in 23S RNA.
Authors: Authors: Moazed D, Robertson JM, Noller HF.
Nature
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Structural analysis of RNA using chemical and enzymatic probing monitored by primer extension.
Authors: Authors: Stern S, Moazed D, Noller HF.
Methods Enzymol
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Chloramphenicol, erythromycin, carbomycin and vernamycin B protect overlapping sites in the peptidyl transferase region of 23S ribosomal RNA.
Authors: Authors: Moazed D, Noller HF.
Biochimie
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Interaction of antibiotics with functional sites in 16S ribosomal RNA.
Authors: Authors: Moazed D, Noller HF.
Nature
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Studies on the architecture and function of 16S rRNA.
Authors: Authors: Noller HF, Stern S, Moazed D, Powers T, Svensson P, Changchien LM.
Cold Spring Harb Symp Quant Biol
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Transfer RNA shields specific nucleotides in 16S ribosomal RNA from attack by chemical probes.
Authors: Authors: Moazed D, Noller HF.
Cell
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