Antisocial, an intracellular adaptor protein, is required for myoblast fusion in Drosophila

Dev Cell. 2001 Nov;1(5):705-15. doi: 10.1016/s1534-5807(01)00084-3.

Abstract

Somatic muscle formation in Drosophila requires fusion of muscle founder cells with fusion-competent myoblasts. In a genetic screen for genes that control muscle development, we identified antisocial (ants), a gene that encodes an ankyrin repeat-, TPR repeat-, and RING finger-containing protein, required for myoblast fusion. In ants mutant embryos, founder cells and fusion-competent myoblasts are properly specified and patterned, but they are unable to form myotubes. ANTS, which is expressed specifically in founder cells, interacts with the cytoplasmic domain of Dumbfounded, a founder cell transmembrane receptor, and with Myoblast city, a cytoskeletal protein, both of which are also required for myoblast fusion. These findings suggest that ANTS functions as an intracellular adaptor protein that relays signals from Dumbfounded to the cytoskeleton during myoblast fusion.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Motifs
  • Amino Acid Sequence
  • Animals
  • Cell Differentiation
  • Cell Fusion
  • Cell Size
  • Cells, Cultured
  • Cloning, Molecular
  • Cytoplasm / chemistry
  • Cytoplasm / metabolism
  • Cytoskeletal Proteins*
  • Drosophila / cytology
  • Drosophila / embryology*
  • Drosophila / genetics
  • Drosophila Proteins / chemistry
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism
  • Embryo, Mammalian / cytology
  • Embryo, Mammalian / metabolism
  • Embryo, Nonmammalian
  • Gene Expression Regulation, Developmental
  • Insect Proteins / chemistry
  • Insect Proteins / genetics
  • Insect Proteins / metabolism
  • Membrane Proteins*
  • Mesoderm / metabolism
  • Mice
  • Molecular Sequence Data
  • Muscle Proteins / chemistry*
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism*
  • Muscles / cytology*
  • Muscles / embryology*
  • Mutation
  • Protein Binding
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Repetitive Sequences, Amino Acid
  • Stem Cells / cytology
  • Stem Cells / metabolism

Substances

  • Cytoskeletal Proteins
  • Drosophila Proteins
  • Insect Proteins
  • Membrane Proteins
  • Muscle Proteins
  • RNA, Messenger
  • kirre protein, Drosophila
  • mbc protein, Drosophila
  • rols protein, Drosophila

Associated data

  • GENBANK/AF440568
  • GENBANK/AF440569