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Biochemistry, Biophysics, and Structural Biology Commons

Open Access. Powered by Scholars. Published by Universities.®

Physiology

2007

Series

Cell cycle

Articles 1 - 2 of 2

Full-Text Articles in Biochemistry, Biophysics, and Structural Biology

Suppression Of P53-Dependent Senescence By The Jnk Signal Transduction Pathway, Madhumita Das, Feng Jiang, Hayla Karen Sluss, Chao Zhang, Kevan M. Shokat, Richard A. Flavell, Roger J. Davis Oct 2007

Suppression Of P53-Dependent Senescence By The Jnk Signal Transduction Pathway, Madhumita Das, Feng Jiang, Hayla Karen Sluss, Chao Zhang, Kevan M. Shokat, Richard A. Flavell, Roger J. Davis

Open Access Articles

The JNK signaling pathway is implicated in the regulation of the AP1 transcription factor and cell proliferation. Here, we examine the role of JNK by using conditional and chemical genetic alleles of the ubiquitously expressed murine genes that encode the isoforms JNK1 and JNK2. Our analysis demonstrates that JNK is not essential for proliferation. However, JNK is required for expression of the cJun and JunD components of the AP1 transcription factor, and JNK-deficient cells exhibit early p53-dependent senescence. These data demonstrate that JNK can act as a negative regulator of the p53 tumor suppressor.


Structural Insights Into The Interaction Of The Evolutionarily Conserved Zpr1 Domain Tandem With Eukaryotic Ef1a, Receptors, And Smn Complexes, Ashwini K. Mishra, Laxman Gangwani, Roger J. Davis, David G. Lambright Aug 2007

Structural Insights Into The Interaction Of The Evolutionarily Conserved Zpr1 Domain Tandem With Eukaryotic Ef1a, Receptors, And Smn Complexes, Ashwini K. Mishra, Laxman Gangwani, Roger J. Davis, David G. Lambright

Open Access Articles

Eukaryotic genomes encode a zinc finger protein (ZPR1) with tandem ZPR1 domains. In response to growth stimuli, ZPR1 assembles into complexes with eukaryotic translation elongation factor 1A (eEF1A) and the survival motor neurons protein. To gain insight into the structural mechanisms underlying the essential function of ZPR1 in diverse organisms, we determined the crystal structure of a ZPR1 domain tandem and characterized the interaction with eEF1A. The ZPR1 domain consists of an elongation initiation factor 2-like zinc finger and a double-stranded beta helix with a helical hairpin insertion. ZPR1 binds preferentially to GDP-bound eEF1A but does not directly influence the ...