The transcription factor Sox9 has essential roles in successive steps of the chondrocyte differentiation pathway and is required for expression of <i>Sox5</i> and <i>Sox6</i>

抄録

<jats:p>To examine whether the transcription factor Sox9 has an essential role during the sequential steps of chondrocyte differentiation, we have used the Cre/<jats:italic>loxP</jats:italic> recombination system to generate mouse embryos in which either Sox9 is missing from undifferentiated mesenchymal cells of limb buds or the <jats:italic>Sox9</jats:italic> gene is inactivated after chondrogenic mesenchymal condensations. Inactivation of<jats:italic>Sox9</jats:italic> in limb buds before mesenchymal condensations resulted in a complete absence of both cartilage and bone, but markers for the different axes of limb development showed a normal pattern of expression. Apoptotic domains within the developing limbs were expanded, suggesting that Sox9 suppresses apoptosis. Expression of<jats:italic>Sox5</jats:italic> and <jats:italic>Sox6</jats:italic>, two other <jats:italic>Sox</jats:italic> genes involved in chondrogenesis, was no longer detected. Moreover, expression of<jats:italic>Runx2</jats:italic>, a transcription factor needed for osteoblast differentiation, was also abolished. Embryos, in which <jats:italic>Sox9</jats:italic> was deleted after mesenchymal condensations, exhibited a severe generalized chondrodysplasia, similar to that in <jats:italic>Sox5</jats:italic>; <jats:italic>Sox6</jats:italic>double-null mutant mice. Most cells were arrested as condensed mesenchymal cells and did not undergo overt differentiation into chondrocytes. Furthermore, chondrocyte proliferation was severely inhibited and joint formation was defective. Although <jats:italic>Indian hedgehog</jats:italic>, <jats:italic>Patched1</jats:italic>, <jats:italic>parathyroid hormone-related peptide</jats:italic> (<jats:italic>Pthrp</jats:italic>), and <jats:italic>Pth/Pthrp receptor</jats:italic> were expressed, their expression was down-regulated. Our experiments further suggested that Sox9 is also needed to prevent conversion of proliferating chondrocytes into hypertrophic chondrocytes. We conclude that Sox9 is required during sequential steps of the chondrocyte differentiation pathway.</jats:p>

収録刊行物

  • Genes & Development

    Genes & Development 16 (21), 2813-2828, 2002-11-01

    Cold Spring Harbor Laboratory

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