Selective role for RGS12 as a Ras/Raf/MEK scaffold in nerve growth factor‐mediated differentiation Components of the mitogen‐activated protein kinase (MAPK)

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Selective role for RGS12 as a Ras/Raf/MEK scaffold in nerve growth factor‐mediated differentiation Prolonged ERK activation by NGF is reduced upon RGS12.

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Selective role for RGS12 as a Ras/Raf/MEK scaffold in nerve growth factor‐mediated differentiation Components of the mitogen‐activated protein kinase (MAPK) cascade identified as RGS12 interactors. (A) RGS12 architecture. Numbering denotes amino‐acid boundaries of domains within rat RGS12. Parentheses denote baits used in yeast two‐hybrid screens against mouse embryo and brain libraries. MEK2 was identified as a PDZ/PTB domain region interactor and A‐Raf was identified as an interactor of the central RGS/RBD domain region (see Supplementary Figure S1). (B) HEK 293T cells were cotransfected with FLAG‐MEK2 and empty vector (‘mock’), or indicated HA‐tagged domain constructs. Anti‐FLAG was used to immunoprecipitate (‘IP’) MEK2 from resultant lysates. Co‐immunoprecipitating proteins and total lysates resolved by SDS–PAGE were immunoblotted (‘IB’) with anti‐FLAG and anti‐HA antibodies. (C) HA‐A‐Raf was cotransfected with empty vector or myc‐RGS12 in COS‐7 cells. (D) HA‐B‐Raf was cotransfected with empty vector, myc‐RGS12, or the isolated tandem RBDs of RGS12 (‘12_RBDs’) in COS‐7 cells. In panels C and D, anti‐myc was used to IP RGS12. Co‐immunoprecipitating proteins and total lysates were then immunoblotted with anti‐myc and anti‐HA antibodies. IF THIS IMAGE HAS BEEN PROVIDED BY OR IS OWNED BY A THIRD PARTY, AS INDICATED IN THE CAPTION LINE, THEN FURTHER PERMISSION MAY BE NEEDED BEFORE ANY FURTHER USE. PLEASE CONTACT WILEY'S PERMISSIONS DEPARTMENT ON PERMISSIONS@WILEY.COM OR USE THE RIGHTSLINK SERVICE BY CLICKING ON THE 'REQUEST PERMISSIONS' LINK ACCOMPANYING THIS ARTICLE. WILEY OR AUTHOR OWNED IMAGES MAY BE USED FOR NON-COMMERCIAL PURPOSES, SUBJECT TO PROPER CITATION OF THE ARTICLE, AUTHOR, AND PUBLISHER. EMBO J, Volume: 26, Issue: 8, Pages: 2029-2040, First published: 22 March 2007, DOI: (10.1038/sj.emboj.7601659)