Al partition of Dicer-1 and Dicer-2 in flies. Carthew described new mutants that are deficient (`RISC-free’) or display enhanced (`high-RISC’) RNAi activity, and discussed how these are being used to define biochemical intermediates of RISC assembly. In the quest to find more players in the pathway, Gary Ruvkun (Harvard Medical School, Boston, USA) and Craig Mello (University of Massachusetts) reported the use of genome-wide RNAi and proteomics, respectively, to identify novel factors involved in RNAi in C. elegans. These include groups of Dicer-interacting proteins and chromatinregulating genes. Mello also touched upon a possible genetic link between heritable forms of gene silencing triggered in the germline by RNAi and the germ-cell-segregating Pgranule bodies in worms because mutations that disrupt Pgranule formation also appears to impair RNAi and compromise siRNA accumulation.The genetics and mechanisms of RNAiIn the principal mechanism of gene silencing by RNAi, the RNA-induced silencing complex (RISC) cleaves target mRNAs that are complementary to the guide siRNA or miRNA within RISC. Studies examining this key event in greater detail were presented at the meeting, and the biogenesis of siRNAs/miRNAs and the steps that lead to the formation of RISC were also topics of great interest. New approaches to identifying other factors with roles in the RNAi pathway were also unveiled. Although it has been known for some time that Dicer generates siRNAs and miRNAs, the lingering question of what enzyme cleaves the mRNAs complementary to siRNAs and miRNAs was answered only recently. Greg Hannon (Cold Spring Harbor Laboratory, New York, USA) described studies showing that recombinant human Argonaute 2 (hAgo2) is sufficient to cleave substrate RNA. Tuschl, John Rossi (Beckman Research Institute of the City of Hope, Duarte, USA), and Elisa Maniataki (University of Pennsylvania, Philadelphia, USA) described many other factors that co-purify with human RISC activity, including Dicer and mammalian homologs of R2D2 and Armitage, proteins known to be involved in RISC maturation in flies. The roles of the novel proteins in RISC maturation and function are under investigation. Hannon and Tuschl also reported that the 5 phosphate of siRNAs is necessary for efficient siRNA incorporation into native RISC; but this requirement can be bypassed when highly purified hAgo2 is assayed instead. Hannon’s enzymaticRegulating chromatin by RNAWhile RNAi is traditionally thought of as a cytoplasmic phenomenon, small RNAs in protozoans, fungi, and plants also function in the nucleus to induce modifications to histones or DNA. This results in the packaging of DNA into transcriptionally silent heterochromatin in plants and fungi, and in the phenomenon of DNA elimination in protozoans. These RNA-based mechanisms are collectivelyGenome PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/26100631 Biology 2005, 6:http://genomebiology.com/2005/6/4/Genome Biology 2005,Volume 6, Issue 4, ArticleLau and Lai 315.Pinometostat supplier referred to as transcriptional gene silencing. Understanding how RNA feeds back to chromatin regulation may be integral to the question of how cells can distinguish euchromatin from silenced heterochromatin, which includes centromeres and transposable elements. Shiv Grewal (National Cancer Institute, NIH, Bethesda, USA) reviewed his groundbreaking work on the proteins associated with the RNAi-based heterochromatic silencing of the mating type (MAT) locus in the fission yeast Schizosaccharomyces pombe, which contains centromeri.
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