Thaler J, Harrison K, Sharma K, Lettieri K, Kehrl J, Pfaff S L
Gene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, California 92037, USA.
Neuron. 1999 Aug;23(4):675-87. doi: 10.1016/s0896-6273(01)80027-1.
Sonic hedgehog (Shh) specifies the identity of both motor neurons (MNs) and interneurons with morphogen-like activity. Here, we present evidence that the homeodomain factor HB9 is critical for distinguishing MN and interneuron identity in the mouse. Presumptive MN progenitors and postmitotic MNs express HB9, whereas interneurons never express this factor. This pattern resembles a composite of the avian homologs MNR2 and HB9. In mice lacking Hb9, the genetic profile of MNs is significantly altered, particularly by upregulation of Chx10, a gene normally restricted to a class of ventral interneurons. This aberrant gene expression is accompanied by topological disorganization of motor columns, loss of the phrenic and abducens nerves, and intercostal nerve pathfinding defects. Thus, MNs actively suppress interneuron genetic programs to establish their identity.
音猬因子(Shh)通过类似形态发生素的活性来确定运动神经元(MNs)和中间神经元的特性。在此,我们提供证据表明,同源结构域因子HB9对于区分小鼠中的运动神经元和中间神经元特性至关重要。假定的运动神经元祖细胞和有丝分裂后的运动神经元表达HB9,而中间神经元从不表达该因子。这种模式类似于鸟类同源物MNR2和HB9的组合。在缺乏Hb9的小鼠中,运动神经元的基因谱显著改变,特别是通过Chx10的上调,Chx10是一个通常仅限于一类腹侧中间神经元的基因。这种异常的基因表达伴随着运动柱的拓扑结构紊乱、膈神经和展神经的缺失以及肋间神经寻路缺陷。因此,运动神经元积极抑制中间神经元的遗传程序以确立其特性。