Gene interactions and pathways from curated databases and text-mining

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ARF1 — JUN

Text-mined interactions from Literome

Kim et al., J Biol Chem 2003 : In addition, ARF4 mediated PLD2 activation leads to dramatic activation of the transcription factor activator protein 1 (AP-1) , and, importantly, ARF4 activity is required for EGF induced activation of cellular AP-1
Ameyar-Zazoua et al., Oncogene 2005 : The ARF promoter is regulated specifically by AP-1 heterodimers containing Fra-1 ... Conversely, inhibition of c-Jun or Fra-1 protein levels resulted in decreased ARF expression ... Thus, AP-1 heterodimers may contribute to the regulation of ARF expression upon oncogenic signaling
Lee et al., J Cell Biol 2008 : Binding of cargo sorting signals to AP-1 enhances its association with ADP ribosylation factor 1-GTP
Suri et al., Methods Mol Biol 2008 : AP-1 recruitment is mediated by the GTPase Arf1 , requires specific lipids, and cargo signals
Wonderlich et al., J Virol 2011 (HIV Infections) : ADP ribosylation factor 1 activity is required to recruit AP-1 to the major histocompatibility complex class I ( MHC-I ) cytoplasmic tail and disrupt MHC-I trafficking in HIV-1 infected primary T cells ... An ARF-1 inhibitor blocked the ability of Nef to recruit AP-1 to the MHC-I cytoplasmic tail, and a dominant active ARF-1 mutant stabilized the Nef-MHC-I-AP-1 complex ... These data support a model in which Nef and ARF-1 stabilize an interaction between MHC-I and AP-1 to disrupt the presentation of HIV-1 epitopes to CTLs
Huser et al., Biochem J 2013 : This localization depends on interaction of clathrin and the adaptor sequence in the amphiphysins and is sensitive to brefeldin A, which inhibits Arf1 dependent AP-1 recruitment
Canagarajah et al., Protein Sci 2013 : Cargo binding by AP-1 is activated by the small GTPase Arf1 , while AP-2 is activated by the phosphoinositide PI ( 4,5 ) P2
Le Borgne et al., J Cell Biol 1997 : Using an in vitro assay that reconstitutes the ARF-1 dependent translocation of cytosolic AP-1 onto membranes of the TGN, we have previously reported that the MPRs are key components for the efficient recruitment of AP-1 ( Le Borgne, R., G. Griffiths, and B. Hoflack
West et al., J Cell Biol 1997 : Surprisingly, however, neither PLD nor neomycin has any effect on the recruitment of AP-1 adaptors onto the TGN, even though AP-1 recruitment is ARF mediated
Ooi et al., J Cell Biol 1998 : ARF1 controls the clathrin coat adaptor AP-1 and the nonclathrin coat COPI, whereas Sar1p controls the nonclathrin coat COPII