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Keeley, S.D.* ; Aires, R.* ; Carbonell Medina, B.* ; Arenas-Gómez, C.M.* ; López-Delgado, A.C.* ; Delgado, J.P.* ; Knopf, F.* ; Kuraku, S.* ; Sandoval-Guzmán, T.

Differential fates of Kazald gene quartet: Ancestral roles in skeletogenesis and regeneration to putative innovations in fish and birds.

iScience 29:114934 (2026)
Verlagsversion Forschungsdaten DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
Gene orthology inference across species is crucial to identify gains and losses of functions. The discovery in axolotl (Ambystoma mexicanum) of a regeneration-associated gene identified as either Kazald1 or Kazald2 led us to investigate its evolution via an extensive cross-species analysis. Molecular phylogeny inference identified the gene as Kazald2 and revealed an undescribed four-member Kazald gene family in jawed vertebrates. Synteny comparisons demonstrated that this family originated in the two-round whole-genome duplication event. Additionally, vertebrate-wide comparisons of Kazald expression, validated in tissues of axolotl, zebrafish, and sharks, uncovered seemingly ancestral connections conserved over jawed vertebrate evolution, and suggested novel putative roles within specific lineages. Our study demonstrates the establishment of the Kazald family in the jawed vertebrate ancestor and elucidates the asymmetry of gene fates of its members. This provides a comprehensive report of this formerly undescribed gene family, offering a solid foundation for its study in diverse species.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Evolutionary Biology ; Evolutionary Developmental Biology ; Evolutionary History ; Natural Sciences; Expression Analysis; Conserved Pathways; Limb Regeneration; Hidden Support; Axolotl; Bone; Alignment; Reconstruction; Transcriptome; Proliferation
ISSN (print) / ISBN 2589-0042
e-ISSN 2589-0042
Zeitschrift iScience
Quellenangaben Band: 29, Heft: 3, Seiten: , Artikelnummer: 114934 Supplement: ,
Verlag Elsevier
Verlagsort Amsterdam ; Bosten ; London ; New York ; Oxford ; Paris ; Philadelphia ; San Diego ; St. Louis
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Pancreatic Islet Research (IPI)
Förderungen Deutsche Forschungsgemeinschaft Eigene Stelle Grant
TU Dresden Graduate Academy
PhD program of the DIGS-ILS
Technische Universität Dresden