The LIM-homeobox gene Lhx5 plays an essential role in the regulation of neu
ronal differentiation and migration during development of the central nervo
us system. Mice lacking Lhx5 function show severely disorganized brain morp
hology and are impaired in cognition and motor coordination. In this study,
we characterized the cDNA and genomic organization of the human LHX5 gene
and analyzed its expression and chromosomal location. The human gene was fo
und to contain five exons encoding a protein composed of 402 amino acids th
at is 98.8% identical to mouse Lhx5. By reverse transcriptase polymerase ch
ain reaction, LHX5 transcripts were detected in fetal brain and in various
regions of the adult central nervous system including the spinal cord, the
thalamus, and the cerebellum. Fluorescence in situ hybridization mapped the
LHX5 gene to chromosome 12, position 12q24.31-24.32. These results provide
a framework for future analysis of possible association of human hereditar
y disorders with mutations in LHX5. (C) 2000 Elsevier Science B.V. All righ
ts reserved.