Department of Molecular Biology, Massachusetts General Hospital, Boston, MA 02114, USA.
Neuron. 2012 Feb 9;73(3):453-65. doi: 10.1016/j.neuron.2011.11.025.
During development, circuits are refined by the dynamic addition and removal of synapses; however, little is known about the molecular mechanisms that dictate where and when synaptic refinement occurs. Here we describe transcriptional mechanisms that pattern remodeling of C. elegans neuromuscular junctions (NMJs). The embryonic GABAergic DD motor neurons remodel their synapses, whereas the later born VD neurons do not. This specificity is mediated by differential expression of a transcription factor (HBL-1), which is expressed in DD neurons but is repressed in VDs by UNC-55/COUP-TF. DD remodeling is delayed in hbl-1 mutants whereas precocious remodeling is observed in mutants lacking the microRNA mir-84, which inhibits hbl-1 expression. Mutations increasing and decreasing circuit activity cause corresponding changes in hbl-1 expression, and corresponding shifts in the timing of DD plasticity. Thus, convergent regulation of hbl-1 expression defines a genetic mechanism that patterns activity-dependent synaptic remodeling across cell types and across developmental time.
在发育过程中,电路通过突触的动态添加和去除进行细化;然而,对于决定突触细化发生的位置和时间的分子机制知之甚少。在这里,我们描述了决定线虫神经肌肉接头(NMJ)重塑的转录机制。DD 运动神经元在胚胎期重塑其突触,而后期出生的 VD 神经元则不这样做。这种特异性是由转录因子(HBL-1)的差异表达介导的,该转录因子在 DD 神经元中表达,但在 VD 神经元中被 UNC-55/COUP-TF 抑制。在 hbl-1 突变体中,DD 重塑被延迟,而在缺乏抑制 hbl-1 表达的 microRNA mir-84 的突变体中,出现了过早的重塑。增加和减少电路活动的突变导致 hbl-1 表达的相应变化,并导致 DD 可塑性的时间相应变化。因此,hbl-1 表达的趋同调控定义了一种遗传机制,该机制为跨细胞类型和跨发育时间的活性依赖性突触重塑提供了模式。