Figliola Rocco, Maione Rossella
Istituto Pasteur-Fondazione Cenci Bolognetti, Dipartimento di Biotecnologie Cellulari ed Ematologia, Sezione di Genetica Molecolare, Università di Roma La Sapienza, Viale Regina Elena, Roma, Italy.
J Cell Physiol. 2004 Sep;200(3):468-75. doi: 10.1002/jcp.20044.
The myogenic factor MyoD induces the expression of the cdk inhibitor p21 to promote cell cycle withdrawal in differentiating myoblasts. Although the cdk inhibitor p57 is also highly expressed in skeletal muscle and is thought to redundantly control myogenesis, little is known about its regulation, that has been suggested to be independent of MyoD. Here we show, for the first time, that MyoD is capable to induce the expression of p57. Intriguingly, this ability is restricted to cells lacking p21, suggesting that the two cdk inhibitors may be expressed in different muscle cell lineages. We also suggest that the functions of p21 and p57 in myoblast cells are only in part redundant. In fact, while the two cdk inhibitors play a similar role in cells undergoing G1 arrest during MyoD-induced differentiation, p57 does not replace p21 in cells escaping G1 arrest and undergoing MyoD-induced apoptosis. This difference can be ascribed both to a different subcellular localization and to a differential ability of the two cdk inhibitors to interact with cell cycle regulators.
肌源性因子MyoD可诱导细胞周期蛋白依赖性激酶(cdk)抑制剂p21的表达,从而促进成肌细胞分化过程中的细胞周期停滞。尽管cdk抑制剂p57在骨骼肌中也高度表达,并且被认为在肌肉生成过程中具有冗余调控作用,但目前对其调控机制知之甚少,且有研究表明其调控机制独立于MyoD。在此,我们首次发现MyoD能够诱导p57的表达。有趣的是,这种能力仅限于缺乏p21的细胞,这表明这两种cdk抑制剂可能在不同的肌肉细胞谱系中表达。我们还认为,p21和p57在成肌细胞中的功能仅部分冗余。事实上,虽然这两种cdk抑制剂在MyoD诱导分化过程中经历G1期停滞的细胞中发挥相似作用,但在逃避G1期停滞并经历MyoD诱导凋亡的细胞中,p57不能替代p21。这种差异既可以归因于不同的亚细胞定位,也可以归因于这两种cdk抑制剂与细胞周期调节因子相互作用的能力差异。