[HTML][HTML] DNA binding partners of YAP/TAZ

MK Kim, JW Jang, SC Bae - BMB reports, 2018 - ncbi.nlm.nih.gov
MK Kim, JW Jang, SC Bae
BMB reports, 2018ncbi.nlm.nih.gov
Hippo signaling plays critical roles in regulation of tissue homeostasis, organ size, and
tumorigenesis by inhibiting YES-associated protein (YAP) and PDZ-binding protein TAZ
through MST1/2 and LATS1/2 pathway. It is also engaged in cross-talk with various other
signaling pathways, including WNT, BMPs, Notch, GPCRs, and Hedgehog to further
modulate activities of YAP/TAZ. Because YAP and TAZ are transcriptional coactivators that
lack DNA-binding activity, both proteins must interact with DNA-binding transcription factors …
Abstract
Hippo signaling plays critical roles in regulation of tissue homeostasis, organ size, and tumorigenesis by inhibiting YES-associated protein (YAP) and PDZ-binding protein TAZ through MST1/2 and LATS1/2 pathway. It is also engaged in cross-talk with various other signaling pathways, including WNT, BMPs, Notch, GPCRs, and Hedgehog to further modulate activities of YAP/TAZ. Because YAP and TAZ are transcriptional coactivators that lack DNA-binding activity, both proteins must interact with DNA-binding transcription factors to regulate target gene’s expression. To activate target genes involved in cell proliferation, TEAD family members are major DNA-binding partners of YAP/TAZ. Accordingly, YAP/TAZ were originally classified as oncogenes. However, YAP might also play tumor-suppressing role. For example, YAP can bind to DNA-binding tumor suppressors including RUNXs and p73. Thus, YAP might act either as an oncogene or tumor suppressor depending on its binding partners. Here, we summarize roles of YAP depending on its DNA-binding partners and discuss context-dependent functions of YAP/TAZ.
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