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Evaluation of the effect of a floxed Neo cassette within the dystroglycan (Dag1) gene

机译:评估dystroglycan(Dag1)基因内的新型Neo盒的效果

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摘要

OBJECTIVE:\udDystroglycan (DG) is an adhesion complex formed by two subunits, α-DG and β-DG. In skeletal muscle, DG is part of the dystrophin-glycoprotein complex that is crucial for sarcolemma stability and it is involved in a plethora of muscular dystrophy phenotypes. Due to the important role played by DG in skeletal muscle stability as well as in a wide variety of other tissues including brain and the peripheral nervous system, it is essential to investigate its genetic assembly and transcriptional regulation.\udRESULTS:\udHerein, we analyze the effect of the insertion of a floxed neomycin (Neo) cassette within the 3' portion of the universally conserved IG1-intron of the DG gene (Dag1). We analyzed the transcription level of Dag1 and the expression of the DG protein in skeletal muscle of targeted mice compared to wild-type and we did not find any alterations that might be attributed to the gene targeting. However, we found an increase of the cross-sectional areas of tibialis anterior that might have some physiological significance that needs to be assessed in the future. Moreover, in targeted mice the skeletal muscle morphology and its regeneration capacity after injury did not show any evident alterations. We confirmed that the targeting of Dag1 with a floxed Neo-cassette did not produce any gross undesired effects.
机译:目的:\ udDystroglycan(DG)是由两个亚基α-DG和β-DG形成的粘附复合物。在骨骼肌中,DG是肌营养不良蛋白-糖蛋白复合物的一部分,它对肌膜稳定至关重要,并且与多种肌营养不良症表型有关。由于DG在骨骼肌以及其他各种组织(包括脑和周围神经系统)的稳定性中起着重要作用,因此研究其遗传装配和转录调控至关重要。\ udRESULTS:\ udHerein在DG基因(Dag1)的普遍保守的IG1内含子的3'部分内插入新霉素(Neo)盒的效果。我们分析了与野生型相比,Dag1的转录水平和靶标小鼠骨骼肌中DG蛋白的表达,我们没有发现任何归因于基因靶向的改变。但是,我们发现胫骨前部的横截面积增加,可能具有某些生理意义,需要在将来进行评估。而且,在靶向小鼠中,损伤后的骨骼肌形态及其再生能力未显示任何明显的改变。我们证实,以Dag1为靶标的新型Neo-cassette不会产生任何明显的不良影响。

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