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Review
. 2010 Jan;10(1):65-76.
doi: 10.1038/nrc2681.

Emerging roles of ATF2 and the dynamic AP1 network in cancer

Pablo Lopez-Bergami  1 , Eric Lau, Ze'ev Ronai
Affiliations
Review

Emerging roles of ATF2 and the dynamic AP1 network in cancer

Pablo Lopez-Bergami et al. Nat Rev Cancer. 2010 Jan.

Erratum in

  • Nat Rev Cancer. 2010 May;10(5):379

Abstract

Cooperation among transcription factors is central for their ability to execute specific transcriptional programmes. The AP1 complex exemplifies a network of transcription factors that function in unison under normal circumstances and during the course of tumour development and progression. This Perspective summarizes our current understanding of the changes in members of the AP1 complex and the role of ATF2 as part of this complex in tumorigenesis.

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Conflict of interest statement

Competing interests statement: The authors declare no competing financial interests.

Figures

Figure 1
Figure 1. Structure and regulation of JUN
JUN is encoded by a 3.34 kb intronless gene, located on chromosome 1 (1p32-p31) and results in the expression of a 334 amino acid protein product composed of four main domains, which are involved in DNA binding, transcription and dimerization. JUN activity is regulated by post-translational modifications, which are largely controlled by components of the MAPK family of serine and threonine kinases, including JUN N-terminal kinase (JNK), ERK and p38 isoforms. JUN is phosphorylated on Ser63 and Ser73 by JNK, increasing its stability and transactivation potential. JNK also phosphorylates Thr91 and Thr93, which are required for DNA binding and activation of its transcriptional activity. JUN is subject to ubiquitylation and this requires phosphorylation at Thr239 by glycogen synthase kinase 3 (GSK3). GSK3 can target JUN only once Ser243 is phosphorylated. Phosphorylation on these sites is required for recruitment of the F-box and WD domain repeated 7 (FBXW7) ubiquitin ligase. Inactivation of GSK3, owing to the activation of ERK and PI3K–Akt signalling cascades results in JUN stabilization,. The effect of GSK3 can be antagonized by the dephosphorylation of Ser243 by calcineurin. JUN can be sumoylated on Lys257 and Lys229, which leads to a reduced transcriptional activity. ERK induces the acetylation of the lysine residues in the JUN DNA binding region, thereby increasing JUN transcriptional activity. Post-translational modifications are indicated as small coloured circles. The four domains are indicated as follows: the δ-domain is orange, the basic region (DNA binding) is blue, the transactivation domain is yellow and the leucine zipper is purple. A, acetylation; dP, dephosphorylation; P, phosphorylation; S, sumoylation.
Figure 2
Figure 2. Mechanisms of JUN degradation
Several mechanisms exist to limit JUN stablity. Under non-stressed conditions, JUN N-terminal kinase (JNK) is tightly bound to JUN, targeting JUN for ubiquitylation and degradation. Activation of JNK by stress results in JUN phosphorylation and dissociation from JNK, enhancing its protein stability, although phosphorylation on Ser63 and Ser73 promotes the F-box and WD domain repeated 7 (FBXW7)-mediated degradation of JUN. As part of a feedforward mechanism, JNK also phosphorylates the E3 ligase Itch in T cells after stimulation, accelerating degradation of JUN and JUNB, independently of Ser63 and Ser73 phosphorylation. Phosphorylation on JUN at Thr239 by glycogen synthase kinase 3 (GsK3) (FIG. 1) allows FBXW7 binding and ubiquitin-mediated degradation by a Skp1-Cullin1-F-box (SCF) complex. Following osmotic stress, MEKK1 can activate JUN N-terminal phosphorylation by activating MKK4, an upstream kinase for JNKs that can also function as a JUN E3 ubiquitin ligase, promoting its ubiquitin–proteasome-dependent degradation (not shown). De-etiolated 1 (DET1) contributes to JUN degradation by promoting the formation of a ubiquitin ligase complex containing DNA damage binding protein 1 (DDB1), cullin 4A (CUL4A), regulator of cullins 1 (ROC1) and constitutively photomorphogenic 1 (COP1). Other mechanisms modulating JUN ubiquitin-mediated degradation have been reported. P, phosphorylation; Ub, ubiquitylation.
Figure 3
Figure 3. Network of AP1 signalling
ERK, JUN N-terminal kinase (JNK) and p38 are predominantly responsible for the phosphorylation and activation of FOS, JUN and ATF2 respectively (black arrows) in response to stress, mitogens or oncogene activation. ERK and JNK also regulate FOS and JUN degradation, respectively (not depicted) and participate in ATF2 activation (dashed arrows). ERK also induces the transcription of FOS through the activation of non-AP1 transcription factors (TFs). Transcription of some AP1 proteins (that is, JUN and FRA1) is regulated by crosstalk among AP1 complexes (red arrows) as well as by autoregulation (circular red arrows).
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References

    1. Lee W, Mitchell P, Tjian R. Purified transcription factor AP1 interacts with TPA-inducible enhancer elements. Cell. 1987;49:741–752. - PubMed
    1. Angel P, et al. Phorbol ester-inducible genes contain a common cis element recognized by a TPA-modulated trans-acting factor. Cell. 1987;49:729–739. - PubMed
    1. Wisdom R. AP1: One switch for many signals. Exp Cell Res. 1999;253:180–185. - PubMed
    1. Eferl R, Wagner EF. AP1: a double-edged sword in tumorigenesis. Nature Rev Cancer. 2003;3:859–868. - PubMed
    1. Angel P, Karin M. The role of Jun, Fos and the AP1 complex in cell-proliferation and transformation. Biochem Biophys Acta. 1991;1072:129–157. - PubMed

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