HLH54F is required for the specification and migration of longitudinal gut muscle founders from the caudal mesoderm of Drosophila.

Development

Mount Sinai School of Medicine, Department of Molecular, Cell and Developmental Biology (currently Developmental and Regenerative Biology), Box 1020, Mount Sinai School of Medicine, New York, NY 10029, USA.

Published: September 2010

AI Article Synopsis

  • HLH54F is a gene in Drosophila (fruit flies) that is key for the development of specific muscle cells in the midgut, originating from the caudal visceral mesoderm (CVM).
  • This gene's expression is controlled by terminal patterning genes and snail, influencing the migration and survival of these muscle precursor cells.
  • Mutations in HLH54F lead to the absence of longitudinal midgut muscles in various stages of development, resulting in significant issues with gut structure and function.

Article Abstract

HLH54F, the Drosophila ortholog of the vertebrate basic helix-loop-helix domain-encoding genes capsulin and musculin, is expressed in the founder cells and developing muscle fibers of the longitudinal midgut muscles. These cells descend from the posterior-most portion of the mesoderm, termed the caudal visceral mesoderm (CVM), and migrate onto the trunk visceral mesoderm prior to undergoing myoblast fusion and muscle fiber formation. We show that HLH54F expression in the CVM is regulated by a combination of terminal patterning genes and snail. We generated HLH54F mutations and show that this gene is crucial for the specification, migration and survival of the CVM cells and the longitudinal midgut muscle founders. HLH54F mutant embryos, larvae, and adults lack all longitudinal midgut muscles, which causes defects in gut morphology and integrity. The function of HLH54F as a direct activator of gene expression is exemplified by our analysis of a CVM-specific enhancer from the Dorsocross locus, which requires combined inputs from HLH54F and Biniou in a feed-forward fashion. We conclude that HLH54F is the earliest specific regulator of CVM development and that it plays a pivotal role in all major aspects of development and differentiation of this largely twist-independent population of mesodermal cells.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2926959PMC
http://dx.doi.org/10.1242/dev.046573DOI Listing

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