与年龄有关的组蛋白 H3.3 积累与小鼠胫骨前肌的抑制性染色质有关

Ryo Masuzawa, Hemilce Karina Rosa Flete, Junya Shimizu, Fuminori Kawano
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摘要

本研究旨在探讨组蛋白变体H3.3与年龄有关的变化及其在小鼠胫骨前肌衰老过程中的作用。H3.3水平随年龄的增长而明显升高,并与H3K27me3水平相关。急性运动成功地上调了 8 周岁小鼠的目标基因表达,而 53 周岁小鼠的目标基因表达没有上调。8 岁小鼠急性运动后,这些基因位点的 H3K27me3 水平升高。然而,在 53 周岁的小鼠中,H3.3 和 H3K27me3 水平在静息状态下升高,不受急性运动的影响。此外,在 8 岁小鼠的骨骼肌中强制表达 H3.3 可使运动功能逐渐改善。结果表明,与年龄相关的 H3.3 积累会诱导小鼠胫骨前肌抑制性染色质的形成。不过,H3.3的积累在增强骨骼肌功能方面似乎也起着积极作用。
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Age-related histone H3.3 accumulation associates with a repressive chromatin in mouse tibialis anterior muscle
The present study aimed to investigate age-related changes in histone variant H3.3 and its role in the aging process of mouse tibialis anterior muscle. H3.3 level significantly increased with age and correlated with H3K27me3 level. Acute exercise successfully upregulated the target gene expression in 8-wk-old mice, whereas no upregulation was noted in 53-wk-old mice. H3K27me3 level was increased at these loci in response to acute exercise in 8-wk-old mice. However, in 53-wk-old mice, H3.3 and H3K27me3 levels were increased at rest and were not affected by acute exercise. Furthermore, forced H3.3 expression in the skeletal muscle of 8-wk-old mice led to a gradual improvement in motor function. The results suggest that age-related H3.3 accumulation induces the formation of repressive chromatin in the mouse tibialis anterior muscle. However, H3.3 accumulation also appears to play a positive role in enhancing skeletal muscle function.
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