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   <subfield code="a">The mammalian Hippo pathway: regulation and function of YAP1 and TAZ</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Manami Kodaka, Yutaka Hata]</subfield>
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   <subfield code="a">The Hippo pathway was originally identified as the signaling that controls organ size in Drosophila, with the core architecture conserved in mammals. In the mammalian Hippo pathway, mammalian Ste20-like kinases (MST1/2) and large tumor suppressor kinases (LATS1/2) regulate transcriptional co-activators, Yes-associated protein (YAP1) and Transcriptional co-activator with a PDZ-binding motif (TAZ). The Hippo pathway was initially thought to be quite straightforward; however, the identification of additional components has revealed its inherent complexity. Regulation of YAP1 and TAZ is not always dependent on MST1/2 and LATS1/2. MST1/2 and LATS1/2 play various YAP1/TAZ-independent roles, while YAP1 and TAZ cross-talk with other signaling pathways. In this review we focus on YAP1 and TAZ and discuss their regulation, function, and the consequences of their dysregulation.</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
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