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pmid: 15581872
The Pak kinases are effectors for the small GTPases Rac and Cdc42 and are divided into two subfamilies. Group I Paks possess an autoinhibitory domain that can suppress their kinase activity in trans. In Drosophila, two Group I kinases have been identified, dPak and Pak3. Rac and Cdc42 participate in dorsal closure of the embryo, a process in which a hole in the dorsal epidermis is sealed through migration of the epidermal flanks over a tissue called the amnioserosa. Dorsal closure is driven in part by an actomyosin contractile apparatus at the leading edge of the epidermis, and is regulated by a Jun amino terminal kinase (JNK) cascade. Impairment of dPak function using either loss-of-function mutations or expression of a transgene encoding the autoinhibitory domain of dPak led to disruption of the leading edge cytoskeleton and defects in dorsal closure but did not affect the JNK cascade. Group I Pak kinase activity in the amnioserosa is required for correct morphogenesis of the epidermis, and may be a component of the signaling known to occur between these two tissues. We conclude that dorsal closure requires Group I Pak function in both the amnioserosa and the epidermis.
Male, MAP Kinase Signaling System, Molecular Sequence Data, Protein Serine-Threonine Kinases, Morphogenesis, Animals, Drosophila Proteins, Humans, Amino Acid Sequence, Phosphotyrosine, Molecular Biology, Cell Shape, Cytoskeleton, In Situ Hybridization, JNK Mitogen-Activated Protein Kinases, Cell Biology, Drosophila melanogaster, Phenotype, Epidermal Cells, Female, Epidermis, Sequence Alignment, Developmental Biology
Male, MAP Kinase Signaling System, Molecular Sequence Data, Protein Serine-Threonine Kinases, Morphogenesis, Animals, Drosophila Proteins, Humans, Amino Acid Sequence, Phosphotyrosine, Molecular Biology, Cell Shape, Cytoskeleton, In Situ Hybridization, JNK Mitogen-Activated Protein Kinases, Cell Biology, Drosophila melanogaster, Phenotype, Epidermal Cells, Female, Epidermis, Sequence Alignment, Developmental Biology
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