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Localization and Regulation of the N Terminal Splice Variant of PGC-1α in Adult Skeletal Muscle Fibers

机译:成人骨骼肌纤维中PGC-1αN末端剪接变体的定位与调控

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摘要

The transcriptional coactivator peroxisome proliferator-activated receptor γ coactivator 1α (PGC-1α) regulates expression of genes for metabolism and muscle fiber type. Recently, a novel splice variant of PGC-1α (NT-PGC-1α, amino acids 1–270) was cloned and found to be expressed in muscle. Here we use Flag-tagged NT-PGC-1α to examine the subcellular localization and regulation of NT-PGC-1α in skeletal muscle fibers. Flag-NT-PGC-1α is located predominantly in the myoplasm. Nuclear NT-PGC-1α can be increased by activation of protein kinase A. Activation of p38 MAPK by muscle activity or of AMPK had no effect on the subcellular distribution of NT-PGC-1α. Inhibition of CRM1-mediated export only caused relatively slow nuclear accumulation of NT-PGC-1α, indicating that nuclear export of NT-PGC-1α may be mediated by both CRM1-dependent and -independent pathways. Together these results suggest that the regulation of NT-PGC-1α in muscle fibers may be very different from that of the full-length PGC-1α, which is exclusively nuclear.
机译:转录共激活因子过氧化物酶体增殖物激活受体γ共激活因子1α(PGC-1α)调节代谢基因和肌肉纤维类型的表达。最近,一种新型的PGC-1α剪接变体(NT-PGC-1α,氨基酸1-270)被克隆并发现在肌肉中表达。在这里,我们使用标志标记的NT-PGC-1α来检查骨骼肌纤维中NT-PGC-1α的亚细胞定位和调控。 Flag-NT-PGC-1α主要位于肌浆中。可以通过激活蛋白激酶A来增加核NT-PGC-1 α 。肌肉活动或AMPK激活p38 MAPK对NT的亚细胞分布没有影响-PGC-1 α 。抑制CRM1介导的出口只会导致NT-PGC-1 α 的核积累相对缓慢,表明NT-PGC-1 的核出口。 α 可能由CRM1依赖性和非依赖性途径介导。这些结果共同表明,NT-PGC-1 α 在肌纤维中的调控可能与全长PGC-1 α ,它完全是核的。

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