The homeobox gene Lbx1 is expressed in migrating hypaxial muscle precursor
cells during development. These precursors delaminate from the lateral edge
of the dermomyotome and form distinct streams that migrate over large dist
ances, using characteristic paths. The targets of migration are limbs, sept
um transversum and the floor of the first branchial arch where the cells fo
rm skeletal muscle of limbs and shoulders, diaphragm and hypoglossal cord,
respectively. We used gene targeting to analyse the function of Lbx1 in the
mouse. Myogenic precursor cells delaminate from the dermomyotome in Lbx1 m
utants, but migrate in an aberrant manner. Most critically affected are mig
rating cells that move to the limbs. Precursor cells that reach the dorsal
limb field are absent. In the ventral limb, precursors are present but dist
ributed in an abnormal manner. As a consequence, at birth some muscles in t
he forelimbs are completely lacking (extensor muscles) or reduced in size (
flexor muscles). Hindlimb muscles are affected strongly, and distal limb mu
scles are more affected than proximal ones. Other migrating precursor cells
heading towards the floor of the first branchial arch move along the appro
priate path in Lbx1 mutants. However, these cells migrate less efficiently
and reduced numbers of precursors reach their distal target. At birth, the
internal lingual muscle is therefore reduced in size. We suggest that Lbx1
controls the expression of genes that are essential for the recognition or
interpretation of cues that guide migrating muscle precursors and maintain
their migratory potential.