Apoptosis of tail muscle during amphibian metamorphosis involves a caspase 9-dependent mechanism

Tail 0301 basic medicine MESH: Mutation MESH: Ta Recombinant Fusion Proteins Xenopus Molecular Sequence Data MESH: Sequence Alignment MESH: Gene Transfer Techniques Apoptosis MESH: Amino Acid Sequence MESH: Research Support, Non-U.S. Gov't 03 medical and health sciences [SDV.BDD] Life Sciences [q-bio]/Development Biology MESH: Recombinant Fusion Proteins Animals MESH: Animals Amino Acid Sequence Muscle, Skeletal [SDV.BDD]Life Sciences [q-bio]/Development Biology bcl-2-Associated X Protein MESH: Muscle, Skeletal MESH: Caspases MESH: Molecular Sequence Data MESH: Apoptosis Gene Transfer Techniques Caspase 9 MESH: Proto-Oncogene Proteins c-bcl-2 Proto-Oncogene Proteins c-bcl-2 Caspases Larva Mutation MESH: Larva Sequence Alignment
DOI: 10.1002/dvdy.20312 Publication Date: 2005-03-11T22:50:29Z
ABSTRACT
The climax of amphibian metamorphosis is marked by thyroid hormone-dependent tadpole tail resorption, implicating apoptosis multiple cell types, including epidermal cells, fibroblasts, nerve and muscles. molecular cascades leading to coordinating the death different types are not fully elucidated. It known that mitochondrial pathway, in particular Bax XR11 genes, regulates balance between survival muscle. However, down-stream factors modulated changes permeability have been studied a functional context. To investigate further mitochondrial-dependent we analyzed regulation role caspase 9 Xenopus tadpoles. We report mRNA expressed before increases during climax. Similarly, at protein level, production active forms muscle tissue as progresses. assess 9, designed dominant-negative protein. Overexpression this abrogates both Bax-induced vitro vivo natural metamorphosis. These findings consolidate model metamorphic directly implicates pathway apoptosome. Developmental Dynamics 233:76–87, 2005. © 2005 Wiley-Liss, Inc.
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