UMass Chan Medical School Faculty Publications

UMMS Affiliation

Department of Biochemistry and Molecular Pharmacology

Publication Date

2000-03-31

Document Type

Article

Subjects

Adenosine Triphosphate; Animals; Base Sequence; Binding Sites; Drosophila; Molecular Sequence Data; Nucleotides; Protein Biosynthesis; RNA Processing, Post-Transcriptional; RNA, Antisense; RNA, Double-Stranded; RNA, Messenger; RNA, Small Interfering

Disciplines

Molecular Biology | Molecular Genetics

Abstract

Double-stranded RNA (dsRNA) directs the sequence-specific degradation of mRNA through a process known as RNA interference (RNAi). Using a recently developed Drosophila in vitro system, we examined the molecular mechanism underlying RNAi. We find that RNAi is ATP dependent yet uncoupled from mRNA translation. During the RNAi reaction, both strands of the dsRNA are processed to RNA segments 21-23 nucleotides in length. Processing of the dsRNA to the small RNA fragments does not require the targeted mRNA. The mRNA is cleaved only within the region of identity with the dsRNA. Cleavage occurs at sites 21-23 nucleotides apart, the same interval observed for the dsRNA itself, suggesting that the 21-23 nucleotide fragments from the dsRNA are guiding mRNA cleavage.

Rights and Permissions

Publisher PDF posted as allowed by the publisher's Open Access Archive policy at http://www.elsevier.com/about/open-access/open-access-policies?a=120972.

DOI of Published Version

10.1016/S0092-8674(00)80620-0

Source

Zamore PD, Tuschl T, Sharp PA, Bartel DP. RNAi: double-stranded RNA directs the ATP-dependent cleavage of mRNA at 21 to 23 nucleotide intervals. Cell. 2000 Mar 31;101(1):25-33. doi:10.1016/S0092-8674(00)80620-0. Link to article on publisher's website

Related Resources

Link to article in PubMed

Journal/Book/Conference Title

Cell

PubMed ID

10778853

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