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Loxl2 and Loxl3 Paralogues Play Redundant Roles during Mouse Development.

Patricia G SantamaríaPierre DubusJosé Bustos-TaulerAlfredo FloristánAlberto Vázquez-NaharroSaleta MoralesAmparo CanoFrancisco Portillo
Published in: International journal of molecular sciences (2022)
Lysyl oxidase-like 2 (LOXL2) and 3 (LOXL3) are members of the lysyl oxidase family of enzymes involved in the maturation of the extracellular matrix. Both enzymes share a highly conserved catalytic domain, but it is unclear whether they perform redundant functions in vivo. In this study, we show that mice lacking Loxl3 exhibit perinatal lethality and abnormal skeletal development. Additionally, analysis of the genotype of embryos carrying double knockout of Loxl2 and Loxl3 genes suggests that both enzymes have overlapping functions during mouse development. Furthermore, we also show that ubiquitous expression of Loxl2 suppresses the lethality associated with Loxl3 knockout mice.
Keyphrases
  • extracellular matrix
  • type diabetes
  • transcription factor
  • adipose tissue
  • metabolic syndrome
  • insulin resistance