Hoxa2 is required for a variety of developmental processes in the branchial
arches and in the hindbrain. We have created a Hoxa2 allele that is about
45% as active in transcription as its wild-type counterpart. This allele, t
ogether with the Hoxa2 null and wild-type alleles, allowed the generation o
f embryos developing in the presence of different levels of Hoxa2 activity.
Analysis of these embryos indicates that in general the hindbrain is more
resistant to Hoxa2 deficiencies than the second branchial arch. Also, withi
n the second arch, proximo-caudal areas are more sensitive than the rostro-
distal. In the hindbrain, basic segmentation and patterning processes seem
to occur normally at Hoxa2 levels as low as 20% of the normal. In addition,
specific neuronal markers along the dorso-ventral axis of the hindbrain se
em differentially affected by reduced Hoxa2 levels. These results provide n
ew clues to understand the role of Hoxa2 in the different embryonic areas w
here it is required. (C) 2001 Elsevier Science Ireland Ltd. All rights rese
rved.