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New Hot Paper Comments

By Prof. Gregory Hannon

ESI Special Topics, March 2003
Citing URL - http://www.esi-topics.com/nhp/2003/march-03-GregoryHannon.html

Prof. Gregory Hannon answers a few questions about this month's new hot paper in the field of Molecular Biology & Genetics.


From •>>March 2003

Field: Molecular Biology & Genetics
Article Title: "Role for a bidentate ribonuclease in the initiation step of RNA interference"
Authors: Bernstein, E;Caudy, AA;Hammond, SM;Hannon, GJ
Journal: NATURE
Volume: 409
Page: 363-366
Year: JAN 18 2001
* Cold Spring Harbor Lab, 1 Bungtown Rd, Cold Spring Harbor, NY 11724 USA.
* Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA.
* Watson Sch Biol Sci, Cold Spring Harbor, NY 11724 USA.

* SUNY Stony Brook, Grad Program Genet, Stony Brook, NY 11794 USA.
* Genetica, Cambridge, MA 01239 USA.

ST:  Why do you think your paper is highly cited?

The paper describes the identification of a key component of the RNA interference pathway.  vRNAi has recently been an area of intense interest both because of the exploitation of this pathway for experimentally manipulating gene expression and because the RNAi machinery plays key roles in genome stability, gene regulation, and the control of development.

ST:  Does it describe a new discovery or a new methodology that's useful to others?

No, but it does help us to understand the mechanistic basis of a widely used methodology. 

ST:  Could you summarize the significance of your paper in layman's terms?

RNA interference is a mechanism of gene silencing that can be triggered by double-stranded RNA.  This is an unusual form of RNA that can result from viral infection and can be characteristic of certain repetitive elements in the genome.  Double-stranded RNA can also be supplied to cells to permit manipulation of gene expression.  In short, we can use dsRNA to switch off the expression of genes at will.  The highly cited paper describes a protein that is part of this machinery.  It is important because an understanding of the RNAi machinery has led to a much greater understanding of the biological impact of RNAi pathways and has led to an ability to exploit this pathway as an experimental and also potentially as a therapeutic tool.

ST:  How did you become involved in this research?

We initially became interested in RNAi because we wanted to understand the mechanism underlying this gene silencing phenomena.  The paper represents one step in a long path toward this goal.End

Gregory Hannon, Professor
Cold Spring Harbor Laboratory
Cold Spring Harbor, NY, USA

ESI Special Topics, March 2003
Citing URL - http://www.esi-topics.com/nhp/2003/march-03-GregoryHannon.html

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