Georgiou Marios, Tear Guy
Molecular Neurobiology Group, MRC Centre for Developmental Neurobiology, Guy's Hospital Campus, King's College, London SE1 1UL, UK.
Development. 2002 Jun;129(12):2947-56. doi: 10.1242/dev.129.12.2947.
In the absence of Commissureless (Comm) function, axons are unable to extend across the central nervous system midline. Comm downregulates levels of Roundabout (Robo), a receptor for the midline repellent Slit, in order to allow axons to cross the midline. comm transcript is expressed at high levels in the midline glia and Comm protein accumulates on axons at the midline. This has led to the hypothesis that Comm moves from the midline glia to the axons, where it can reduce Robo levels. We have found that expression of Comm in the midline cells is unable to rescue the comm phenotype and that tagged versions of Comm are not transferred to axons. A re-examination of Comm protein expression and the use of targeted RNA interference reveal that correct midline crossing requires that Comm is expressed in the commissural axons and midline glia. We suggest that accumulation of Comm protein at the midline spatially limits Comm activity and prevents it from being active on the contralateral side of the central nervous system.
在缺乏无连合蛋白(Comm)功能的情况下,轴突无法延伸穿过中枢神经系统中线。Comm会下调Roundabout(Robo)的水平,Robo是中线排斥分子Slit的受体,以此使轴突能够穿过中线。comm转录本在中线胶质细胞中高水平表达,且Comm蛋白在中线处的轴突上积累。这导致了一种假说,即Comm从中线胶质细胞转移到轴突上,在那里它可以降低Robo的水平。我们发现,在中线细胞中表达Comm无法挽救comm表型,并且Comm的标记版本不会转移到轴突上。对Comm蛋白表达的重新检查以及使用靶向RNA干扰表明,正确的中线交叉需要Comm在连合轴突和中线胶质细胞中表达。我们认为,Comm蛋白在中线处的积累在空间上限制了Comm的活性,并阻止其在中枢神经系统的对侧发挥作用。