Ribozyme- and siRNA-mediated suppression of RGS-containing RhoGEF proteins.

Abstract:

:Given recent efforts to determine the sequence information on thousands of genes in the human genome, the current challenge is to identify the functions of these genes, including those encoding the regulator of G-protein signaling protein gene superfamily, and to establish their roles in particular signaling pathways in a native system. Increasingly, reverse genetic approaches are being used to address these questions. This article compares two powerful approaches [ribozyme and "short interfering" RNA (siRNA) techniques] under identical conditions for the first report on the suppression of endogenous RGS domain-containing RhoGEFs. The siRNA technique was found to be much more potent than ribozyme targeting at the same mRNA site of RGS-RhoGEFs. Also, the three siRNAs targeting LARG, PDZ-RhoGEF, and p115-RhoGEF are able to discriminate the closely related sequences within this RGS-RhoGEF gene family.

journal_name

Methods Enzymol

journal_title

Methods in enzymology

authors

Wang Q,Liu M,Kozasa T,Rothestein JD,Sternweis PC,Neubig RR

doi

10.1016/S0076-6879(04)89015-3

subject

Has Abstract

pub_date

2004-01-01 00:00:00

pages

244-65

eissn

0076-6879

issn

1557-7988

pii

S0076687904890153

journal_volume

389

pub_type

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