Axial skeletal patterning in mice lacking all paralogous group 8 Hox genes

• Published in: Development (Cambridge) Vol. 128; no. 10; pp. 1911 - 1921
• Main Authors: Akker, Eric van den, Fromental-Ramain, Catherine, Graaff, Wim de, Le Mouellic, Hervé, Brûlet, Philippe, Chambon, Pierre, Deschamps, Jacqueline
• Format: Journal Article
• Language: English
• Published: England The Company of Biologists Limited 15-05-2001; Company of Biologists
• Subjects: Animals; Animals, Newborn; Base Sequence; Body Patterning - genetics; Bone and Bones - abnormalities; Bone Development - genetics; DNA Primers - genetics; Female; Gene Expression Regulation, Developmental; Genes, Homeobox; Genetics; Homeodomain Proteins - genetics; Hox8 gene; Hoxb8 gene; Hoxc8 gene; Hoxd8 gene; Life Sciences; Male; Mesoderm - metabolism; Mice; Mice, Knockout; Phenotype; Spine - embryology; Transcription Factors - genetics
• ISSN: 0950-1991; 1477-9129
• DOI: 10.1242/dev.128.10.1911

We present a detailed study of the genetic basis of mesodermal axial patterning by paralogous group 8 Hox genes in the mouse. The phenotype of Hoxd8 loss-of-function mutants is presented, and compared with that of Hoxb8- and Hoxc8-null mice. Our analysis of single mutants reveals common features for the Hoxc8 and Hoxd8 genes in patterning lower thoracic and lumbar vertebrae. In the Hoxb8 mutant, more anterior axial regions are affected. The three paralogous Hox genes are expressed up to similar rostral boundaries in the mesoderm, but at levels that strongly vary with the axial position. We find that the axial region affected in each of the single mutants mostly corresponds to the area with the highest level of gene expression. However, analysis of double and triple mutants reveals that lower expression of the other two paralogous genes also plays a patterning role when the mainly expressed gene is defective. We therefore conclude that paralogous group 8 Hox genes are involved in patterning quite an extensive anteroposterior (AP) axial region. Phenotypes of double and triple mutants reveal that Hoxb8, Hoxc8 and Hoxd8 have redundant functions at upper thoracic and sacral levels, including positioning of the hindlimbs. Interestingly, loss of functional Hoxb8 alleles partially rescues the phenotype of Hoxc8- and Hoxc8/Hoxd8-null mutants at lower thoracic and lumbar levels. This suggests that Hoxb8 affects patterning at these axial positions differently from the other paralogous gene products. We conclude that paralogous Hox genes can have a unique role in patterning specific axial regions in addition to their redundant function at other AP levels.