Eshraghi Mehdi, McFall Emily, Gibeault Sabrina, Kothary Rashmi
Regenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada
University of Ottawa Centre for Neuromuscular Disease, Ottawa, Ontario, Canada
Hum Mol Genet. 2016 Oct 15;25(20):4494-4506. doi: 10.1093/hmg/ddw278.
Spinal muscular atrophy (SMA) is caused by mutations or deletions in the Survival Motor Neuron 1 (SMN1) gene in humans. Modifiers of the SMA symptoms have been identified and genetic background has a substantial effect in the phenotype and survival of the severe mouse model of SMA. Previously, we generated the less severe Smn2B/- mice on a mixed genetic background. To assess the phenotype of Smn deficiency on a pure genetic background, we produced Smn2B/2B congenic mice on either the C57BL/6 (BL6) or FVB strain background and characterized them at the 6th generation by breeding to Smn+/- mice. Smn2B/- mice from these crosses were evaluated for growth, survival, muscle atrophy, motor neuron loss, motor behaviour, and neuromuscular junction pathology. FVB Smn2B/- mice had a shorter life span than BL6 Smn2B/- mice (median of 19 days vs. 25 days). Similarly, all other defects assessed occurred at earlier stages in FVB Smn2B/-mice when compared to BL6 Smn2B/-mice. However, there were no differences in Smn protein levels in the spinal cords of these mice. Interestingly, levels of Plastin 3, a putative modifier of SMA, were significantly induced in spinal cords of BL6 Smn2B/- mice but not of FVB Smn2B/-mice. Our studies demonstrate that the phenotype in Smn2B/-mice is more severe in the FVB background than in the BL6 background, which could potentially be explained by the differential induction of genetic modifiers.
脊髓性肌萎缩症(SMA)是由人类生存运动神经元1(SMN1)基因的突变或缺失引起的。已确定了SMA症状的修饰因子,并且遗传背景对严重SMA小鼠模型的表型和存活有重大影响。此前,我们在混合遗传背景上培育出了症状较轻的Smn2B/-小鼠。为了评估纯合遗传背景下Smn缺乏的表型,我们在C57BL/6(BL6)或FVB品系背景上培育出了Smn2B/2B同源基因小鼠,并在第6代通过与Smn+/-小鼠杂交对其进行了表征。对这些杂交产生的Smn2B/-小鼠进行了生长、存活、肌肉萎缩、运动神经元丧失、运动行为和神经肌肉接头病理学评估。FVB Smn2B/-小鼠的寿命比BL6 Smn2B/-小鼠短(中位数分别为19天和25天)。同样,与BL6 Smn2B/-小鼠相比,FVB Smn2B/-小鼠中评估的所有其他缺陷都出现在更早阶段。然而,这些小鼠脊髓中Smn蛋白水平没有差异。有趣的是,SMA的一个假定修饰因子Plastin 3的水平在BL6 Smn2B/-小鼠的脊髓中显著诱导,但在FVB Smn2B/-小鼠中未诱导。我们的研究表明,Smn2B/-小鼠在FVB背景下的表型比在BL6背景下更严重,这可能是由遗传修饰因子的差异诱导所解释的。