SCALLOPED Interacts with YORKIE, the Nuclear Effector of the Hippo Tumor-Suppressor Pathway in Drosophila

Autor: Youlian Goulev, Jean Daniel Fauny, Beatriz Gonzalez-Marti, Joël Silber, Alain Zider, Domenico Flagiello
Přispěvatelé: Institut Jacques Monod (IJM (UMR_7592)), Université Paris Diderot - Paris 7 (UPD7)-Centre National de la Recherche Scientifique (CNRS), the Association Française contre les Myopathies, the Association pour la Recherche sur le Cancer
Jazyk: angličtina
Rok vydání: 2008
Předmět:
animal structures
Mutant
DEVBIO
Protein Serine-Threonine Kinases
Biology
General Biochemistry
Genetics and Molecular Biology

law.invention
03 medical and health sciences
0302 clinical medicine
Transcription (biology)
law
Morphogenesis
Animals
Drosophila Proteins
Humans
Wings
Animal

Transcription factor
Cell Proliferation
030304 developmental biology
Genetics
0303 health sciences
Hippo signaling pathway
Agricultural and Biological Sciences(all)
Effector
Schneider 2 cells
Biochemistry
Genetics and Molecular Biology(all)

Tumor Suppressor Proteins
fungi
Intracellular Signaling Peptides and Proteins
Nuclear Proteins
YAP-Signaling Proteins
[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry
Molecular Biology/Molecular biology

Cell biology
body regions
SIGNALING
Trans-Activators
Suppressor
Drosophila
General Agricultural and Biological Sciences
Protein Kinases
030217 neurology & neurosurgery
Nuclear localization sequence
HeLa Cells
Signal Transduction
Transcription Factors
Zdroj: Current Biology-CB
Current Biology-CB, Elsevier, 2008, epub ahead of print. ⟨10.1016/j.cub.2008.02.034⟩
ISSN: 0960-9822
1879-0445
Popis: International audience; In Drosophila, SCALLOPED (SD) belongs to a family of evolutionarily conserved proteins characterized by the presence of a TEA/ATTS DNA-binding domain [1, 2]. SD physically interacts with the product of the vestigial (vg) gene, where the dimer functions as a master gene controlling wing formation [3, 4]. The VG-SD dimer activates the transcription of several specific wing genes, including sd and vg themselves [5, 6]. The dimer drives cell-cycle progression by inducing expression of the dE2F1 transcription factor [7], which regulates genes involved in DNA replication and cell-cycle progression. Recently, YORKIE (YKI) was identified as a transcriptional coactivator that is the downstream effector of the Hippo signaling pathway, which controls cell proliferation and apoptosis in Drosophila[8]. We identified SD as a partner for YKI. We show that interaction between YKI and SD increases SD transcriptional activity both ex vivo in Drosophila S2 cells and in vivo in Drosophila wing discs and promotes YKI nuclear localization. We also show that YKI overexpression induces vg and dE2F1 expression and that proliferation induced by YKI or by a dominant-negative form of FAT in wing disc is significantly reduced in a sd hypomorphic mutant context. Contrary to YKI, SD is not required in all imaginal tissues. This indicates that YKI-SD interaction acts in a tissue-specific fashion and that other YKI partners must exist.
Databáze: OpenAIRE