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首页> 外文期刊>FEBS letters. >Alternative splicing within the I-II loop controls surface expression of T-type Ca(v)3.1 calcium channels.
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Alternative splicing within the I-II loop controls surface expression of T-type Ca(v)3.1 calcium channels.

机译:I-II环内的选择性剪接控制T型Ca(v)3.1钙通道的表面表达。

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Molecular diversity of T-type/Ca(v)3 Ca(2+) channels is created by expression of three genes and alternative splicing of those genes. Prompted by the important role of the I-II linker in gating and surface expression of Ca(v)3 channels, we describe here the properties of a novel variant that partially deletes this loop. The variant is abundantly expressed in rat brain, even exceeding transcripts with the complete exon 8. Electrophysiological analysis of the Delta8b variant revealed enhanced current density compared to Ca(v)3.1a, but similar gating. Luminometry experiments revealed an increase in the expression of Delta8b channels at the plasma membrane. We conclude that alternative splicing of Ca(v)3 channels regulates surface expression and may underlie disease states in which T-channel current density is increased.
机译:T型/ Ca(v)3 Ca(2+)通道的分子多样性是通过三个基因的表达和这些基因的可变剪接产生的。由I-II接头在Ca(v)3通道的门控和表面表达中的重要作用提示,我们在这里描述了部分删除该环的新型变异的性质。该变体在大鼠脑中大量表达,甚至超过了完整外显子8的转录本。对Delta8b变体的电生理分析表明,与Ca(v)3.1a相比,电流密度提高了,但门控相似。发光实验表明质膜上Delta8b通道的表达增加。我们得出结论,Ca(v)3通道的选择性剪接调节表面表达,并可能是其中T通道电流密度增加的疾病状态的基础。

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