Extensive loss of HoxA/D genes does not disrupt anterior vertebral patterning in zebrafish
- 1Saitama University
Abstract
Hox genes play central roles in specifying positional identities along the vertebrate anterior-posterior axis. In mice, genetic analyses have demonstrated that Hox genes distributed among the four Hox clusters contribute to vertebral patterning, with extensive functional redundancy among paralogous genes. Our previous genetic analysis in zebrafish identified important roles for HoxB- and HoxC-related genes in specifying anterior vertebral identities, whereas the contributions of HoxA- and HoxD-related genes remained unresolved. Here, we examined adult zebrafish carrying extensive combinations of hoxaa, hoxab, and hoxda cluster deletions and generated five-gene homozygous mutants carrying frameshift mutations in hoxa3a, hoxa4a, hoxa5a, hoxd3a, and hoxd4a. X-ray micro-CT analysis revealed no obvious anterior vertebral transformations in either the compound cluster mutants or the five-gene mutants. Together with our previous findings, these results suggest that vertebral patterning functions are distributed unevenly among zebrafish hox clusters, with a predominant contribution from HoxB/C-related genes.
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BibTeX
@misc{tani2026extensive,
title = {{Extensive loss of HoxA/D genes does not disrupt anterior vertebral patterning in zebrafish}},
author = {T. Tani and A. Maeno and H. Nakazawa and T. Fujibayashi and K. Suda and A. Kawamura},
howpublished = {bioRxiv},
year = {2026},
month = sep,
doi = {10.64898/2026.09.09.750522},
url = {https://www.biorxiv.org/content/10.64898/2026.09.09.750522v1},
note = {CC BY-NC-ND},
}
RIS
TY - UNPB
TI - Extensive loss of HoxA/D genes does not disrupt anterior vertebral patterning in zebrafish
AU - T. Tani
AU - A. Maeno
AU - H. Nakazawa
AU - T. Fujibayashi
AU - K. Suda
AU - A. Kawamura
PY - 2026
DA - 2026/09/09
PB - bioRxiv
DO - 10.64898/2026.09.09.750522
UR - https://www.biorxiv.org/content/10.64898/2026.09.09.750522v1
AB - Hox genes play central roles in specifying positional identities along the vertebrate anterior-posterior axis. In mice, genetic analyses have demonstrated that Hox genes distributed among the four Hox clusters contribute to vertebral patterning, with extensive functional redundancy among paralogous genes. Our previous genetic analysis in zebrafish identified important roles for HoxB- and HoxC-related genes in specifying anterior vertebral identities, whereas the contributions of HoxA- and HoxD-related genes remained unresolved. Here, we examined adult zebrafish carrying extensive combinations of hoxaa, hoxab, and hoxda cluster deletions and generated five-gene homozygous mutants carrying frameshift mutations in hoxa3a, hoxa4a, hoxa5a, hoxd3a, and hoxd4a. X-ray micro-CT analysis revealed no obvious anterior vertebral transformations in either the compound cluster mutants or the five-gene mutants. Together with our previous findings, these results suggest that vertebral patterning functions are distributed unevenly among zebrafish hox clusters, with a predominant contribution from HoxB/C-related genes.
ER -