Aruga J, Mizugishi K, Koseki H, Imai K, Balling R, Noda T, Mikoshiba K
Molecular Neurobiology Laboratory, Tsukuba Life Science Center, RIKEN, Tsukuba-shi, Ibaraki, Japan.
Mech Dev. 1999 Dec;89(1-2):141-50. doi: 10.1016/s0925-4773(99)00220-8.
Skeletal abnormalities are described that appeared in Zic1-deficient mice. These mice show multiple abnormalities in the axial skeleton. The deformities are severe in the dorsal parts of the vertebrae, vertebral arches, but less so in the vertebral bodies (spina bifida occulta). The proximal ribs are deformed having ectopic processes. The abnormalities found in the vertebral arches can be traced back to disturbed segmental patterns of dorsal sclerotome. The Zic1/Gli3 double mutants showed severe abnormalities of vertebral arches not found in single mutants. The abnormalities in the vertebral arches were less severe in Zic1/Pax1 mutants than Zic1/Gli3 mutants, but significantly more pronounced than in Zic1 single mutants. The three genes may act synergistically in the development of the vertebral arches.
描述了Zic1基因缺陷小鼠出现的骨骼异常情况。这些小鼠在中轴骨骼上表现出多种异常。椎骨、椎弓的背部畸形严重,但椎体(隐性脊柱裂)的畸形较轻。近端肋骨变形,有异位突起。在椎弓中发现的异常可追溯到背侧生骨节的节段模式紊乱。Zic1/Gli3双突变体表现出单突变体中未出现的严重椎弓异常。Zic1/Pax1突变体的椎弓异常比Zic1/Gli3突变体轻,但比Zic1单突变体明显更显著。这三个基因可能在椎弓发育中协同作用。