Yang J S, Bennett P B, Makita N, George A L, Barchi R L
Mahoney Institute of Neurological Sciences, University of Pennsylvania School of Medicine, Philadelphia 19104.
Neuron. 1993 Nov;11(5):915-22. doi: 10.1016/0896-6273(93)90121-7.
Transcripts homologous to the rat brain sodium channel beta subunit (beta 1) are prominently expressed in both innervated and denervated adult skeletal muscle and in heart, but not in neonatal skeletal or cardiac muscle. Regulation of beta 1 mRNA expression closely parallels that of SkM1 alpha during development, after denervation in adult muscle, and in primary muscle culture, but does not follow SkM2 expression under any condition examined. In oocytes, beta 1 interacts functionally with SkM1 to modulate the abnormally slow inactivation kinetics observed with this alpha subunit expressed alone. We conclude that a common beta 1 subunit is expressed in skeletal muscle, heart, and brain and that in skeletal muscle, this subunit is specifically associated with the SkM1, rather than the SkM2, sodium channel isoform.
与大鼠脑钠通道β亚基(β1)同源的转录本在成年受神经支配和去神经支配的骨骼肌以及心脏中均有显著表达,但在新生骨骼肌或心肌中不表达。在发育过程中、成年肌肉去神经支配后以及原代肌肉培养中,β1 mRNA表达的调节与SkM1α的调节密切平行,但在任何检测条件下均不跟随SkM2的表达。在卵母细胞中,β1与SkM1在功能上相互作用,以调节单独表达该α亚基时观察到的异常缓慢的失活动力学。我们得出结论,一个共同的β1亚基在骨骼肌、心脏和脑中表达,并且在骨骼肌中,该亚基与钠通道亚型SkM1而非SkM2特异性相关。