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Field Value
 
Creator Suryawanshi, H
Scaria, V
Maiti, S
 
Subject Biochemistry & Molecular Biology
 
Description MicroRNAs (miRNAs) are now recognized as one of the major class of gene regulatory molecules in eukaryotic cells. Aberrant miRNA expression has been implicated in many human diseases. Herein, we exploit the site-specific cleavage ability of hammerhead ribozymes to design synthetic ribozymes and establish that they can cleave miRNA, thereby inhibiting miRNA function. We also used modified ribozymes where a 3'-3'-linked nucleotide "cap" (inverted T) was added and few ribonucleotides were changed to 2'-O-methyl nucleotides. The modified ribozyme was more efficient at inhibiting miR-21 than the wild type ribozyme.
 
Publisher ROYAL SOC CHEMISTRYCAMBRIDGETHOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND
 
Date 2011-09-20T12:07:12Z
2011-09-20T12:07:12Z
2010
 
Type Article
 
Identifier MOLECULAR BIOSYSTEMS
1742-206X
http://hdl.handle.net/123456789/13150
 
Language English