HoxB genes regulate neuronal delamination in the trunk neural tube by controlling the expression of Lzts1
Author(s) -
Axelle Wilmerding,
Lucrezia Rinaldi,
Nathalie Caruso,
Laure Lo Re,
Emilie Bonzom,
Andrew J. Saurin,
Yacine Graba,
Marie-Claire Delfini
Publication year - 2021
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.15
H-Index - 36
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.195404
Subject(s) - hox gene , biology , neural tube , spinal cord , ectopic expression , gene , microbiology and biotechnology , anatomy , trunk , gene expression , neuroscience , genetics , embryo , ecology
Differential Hox gene expression is central for specification of axial neuronal diversity in the spinal cord. Here, we uncover an additional function of Hox proteins in the developing spinal cord, restricted to B cluster Hox genes. We found that members of the HoxB cluster are expressed in the trunk neural tube of chicken embryo earlier than Hox from the other clusters, with poor antero-posterior axial specificity and with overlapping expression in the intermediate zone (IZ). Gain-of-function experiments of HoxB4, HoxB8 and HoxB9, respectively, representative of anterior, central and posterior HoxB genes, resulted in ectopic progenitor cells in the mantle zone. The search for HoxB8 downstream targets in the early neural tube identified the leucine zipper tumor suppressor 1 gene (Lzts1), the expression of which is also activated by HoxB4 and HoxB9. Gain- and loss-of-function experiments showed that Lzts1, which is expressed endogenously in the IZ, controls neuronal delamination. These data collectively indicate that HoxB genes have a generic function in the developing spinal cord, controlling the expression of Lzts1 and neuronal delamination.
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