ZFIN ID: ZDB-PUB-190601-3
Yap1b, a divergent Yap/Taz family member, cooperates with yap1 in survival and morphogenesis via common transcriptional targets
Vázquez-Marín, J., Gutiérrez-Triana, J.A., Almuedo-Castillo, M., Buono, L., Gómez-Skarmeta, J.L., Mateo, J.L., Wittbrodt, J., Martínez-Morales, J.R.
Date: 2019
Source: Development (Cambridge, England)   146(13): (Journal)
Registered Authors: Gómez-Skarmeta, José Luis
Keywords: Apoptosis, Chromatin-binding, DamID-seq, Morphogenesis, Transcriptional-activation-domain, Yap/Taz
Microarrays: GEO:GSE120531
MeSH Terms:
  • Animals
  • Animals, Genetically Modified
  • Embryo Loss/genetics*
  • Embryo Loss/veterinary
  • Embryo, Nonmammalian
  • Gene Expression Regulation, Developmental*
  • Intracellular Signaling Peptides and Proteins/genetics
  • Intracellular Signaling Peptides and Proteins/physiology
  • Morphogenesis/genetics*
  • Mutation
  • Oryzias/embryology
  • Oryzias/genetics
  • Protein Domains/genetics
  • Protein Isoforms/chemistry
  • Protein Isoforms/genetics
  • Protein Isoforms/physiology
  • Trans-Activators/chemistry
  • Trans-Activators/genetics
  • Trans-Activators/physiology*
  • Transcription Factors/chemistry
  • Transcription Factors/genetics
  • Transcription Factors/physiology
  • Zebrafish/embryology
  • Zebrafish/genetics
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/physiology*
PubMed: 31142542 Full text @ Development
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ABSTRACT
Yap1/Taz are well-known Hippo effectors triggering complex transcriptional programs controlling growth, survival, and cancer progression. Here we describe yap1b, a new Yap1/Taz family member with a unique transcriptional activation domain that cannot be phosphorylated by Src/Yes kinases. We show that yap1b evolved specifically in euteleosts (i.e. including medaka but not zebrafish) by duplication and adaptation of yap1. Using DamID-seq we generated maps of chromatin occupancy for Yap1, Taz (Wwtr1), and Yap1b, in gastrulating zebrafish and medaka embryos. Our comparative analyses uncover the genetic programs controlled by yap family proteins during early embryogenesis, and show largely overlapping targets for Yap1 and Yap1b. CRISPR/Cas9-induced mutation of yap1b in medaka does not result in an overt phenotype during embryogenesis or adulthood. However, yap1b mutation strongly enhances the embryonic malformations observed in yap1 mutants. Thus yap1-/-; yap1b-/- double mutants display more severe body flattening, eye misshaping, and increased apoptosis than yap1-/- single mutants; thus revealing overlapping gene functions. Our results indicate that, despite its divergent transactivation domain, Yap1b cooperates with Yap1 to regulate cell survival and tissue morphogenesis during early development.
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