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Mutation in slowmo causes defects in Drosophila larval locomotor behaviour.

Invert. Neurosci.2004 Oct;5(2):65-75. doi:10.1007/s10158-003-0028-y. Epub 2003 Dec 13
Ahmet Carhan 1 , Simon Reeve , Chris T Dee , Richard A Baines , Kevin G Moffat
Ahmet Carhan 1 , Simon Reeve , Chris T Dee , Richard A Baines , Kevin G Moffat

[No authors listed]

Author information
  • 1 Department of Biological Sciences, University of Warwick, CV4 7AL, Coventry, UK.

摘要


We have identified a mutant slowmotion phenotype in first instar larval peristaltic behaviour of Drosophila. By the end of embryogenesis and during early first instar phases, slowmo mutant animals show a marked decrease in locomotory behaviour, resulting from both a reduction in number and rate of peristaltic contractions. Inhibition of neurotransmitter release, using targeted expression of tetanus toxin light chain (TeTxLC), in the slowmo neurons marked by an enhancer-trap results in a similar phenotype of largely absent or uncoordinated contractions. Cloning of the slowmo gene identifies a product related to a family of proteins of unknown function. We show that Slowmo is associated with mitochondria, indicative of it being a mitochondrial protein, and that during embryogenesis and early larval development is restricted to the nervous system in a subset of cells. The enhancer-trap marks a cellular component of the CNS that is seemingly required to regulate peristaltic movement.