The long-term goal of this work is to understand how the RNA interference (RNAi) pathway directs the formation of silent heterochromatic DNA domains. Heterochromatin is a conserved feature of eukaryotic chromosomes and plays important roles in regulation of gene expression and maintenance of chromosome stability in organisms ranging from yeast to human. In the fission yeast Schiozosaccharomyces pombe, the RITS (RNA-induced transcriptional silencing) complex uses small interfering RNAs (siRNAs) to target specific chromosome regions by base pairing interactions with nascent noncoding RNAs. This targeting is coupled to histone H3 lysine 9 (H3K9) methylation and the recruitment of proteins that mediate silencing. RITS also mediates siRNA amplification by recruiting the RNA-dependent RNA polymerase complex (RDRC) to promote the synthesis of double stranded RNA, which is cleaved into siRNAs by the Dicer ribonuclease. It has remained unclear how noncoding RNAs give rise to small RNA triggers that initiate RNAi, how RNA participates in the recruitment of histone H3K9 methyltransferase complex (CLRC), and how the recruitment of downstream factors such as HP1 proteins leads to transcriptional gene silencing. In this proposal we will use a combination of in vivo approaches and biochemical assays to investigate (1) the functional elements in centromeric RNAs and their associated factors that trigger RNAi, (2) the mechanism of siRNA-mediated chromatin methylation, and (3) the molecular mechanism of heterochromatin-dependent transcriptional gene silencing. The ultimate goal of these studies is a complete molecular understanding of gene silencing.
Noncoding RNAs and RNAi play widely conserved roles in the regulation of gene expression and genome stability in eukaryotes and contribute to normal development and disease progression in humans. The conservation of RNAi and HP1-associated heterochromatic domains in organisms ranging from fission yeast to human suggests that the principles developed by our proposed studies for the fission yeast complexes will apply in other settings. A basic understanding of the mechanisms that mediate RNA-mediated heterochromatin formation will not only provide a frame work for understanding how the process can fail, but also provides the substrate and knowledge to design therapeutic strategies based on intervention.
|Wang, Xiaoyi; Moazed, Danesh (2017) DNA sequence-dependent epigenetic inheritance of gene silencing and histone H3K9 methylation. Science 356:88-91|
|Jih, Gloria; Iglesias, Nahid; Currie, Mark A et al. (2017) Unique roles for histone H3K9me states in RNAi and heritable silencing of transcription. Nature 547:463-467|
|Banday, Shahid; Farooq, Zeenat; Rashid, Romana et al. (2016) Role of Inner Nuclear Membrane Protein Complex Lem2-Nur1 in Heterochromatic Gene Silencing. J Biol Chem 291:20021-9|
|Jain, Ruchi; Iglesias, Nahid; Moazed, Danesh (2016) Distinct Functions of Argonaute Slicer in siRNA Maturation and Heterochromatin Formation. Mol Cell 63:191-205|
|Holoch, Daniel; Moazed, Danesh (2015) Small-RNA loading licenses Argonaute for assembly into a transcriptional silencing complex. Nat Struct Mol Biol 22:328-35|
|Martienssen, Robert; Moazed, Danesh (2015) RNAi and heterochromatin assembly. Cold Spring Harb Perspect Biol 7:a019323|
|Gerace, Erica; Moazed, Danesh (2015) Affinity Purification of Protein Complexes Using TAP Tags. Methods Enzymol 559:37-52|
|Ragunathan, Kaushik; Jih, Gloria; Moazed, Danesh (2015) Epigenetics. Epigenetic inheritance uncoupled from sequence-specific recruitment. Science 348:1258699|
|Gerace, Erica; Moazed, Danesh (2015) Affinity Pull-Down of Proteins Using Anti-FLAG M2 Agarose Beads. Methods Enzymol 559:99-110|
|Holoch, Daniel; Moazed, Danesh (2015) RNA-mediated epigenetic regulation of gene expression. Nat Rev Genet 16:71-84|
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