Furukawa Yoshiaki, Kaneko Kumi, Matsumoto Gen, Kurosawa Masaru, Nukina Nobuyuki
Laboratory for Structural Neuropathology, Brain Science Institute, RIKEN, Wako, Saitama 351-0198, Japan.
J Neurosci. 2009 Apr 22;29(16):5153-62. doi: 10.1523/JNEUROSCI.0783-09.2009.
A pathological hallmark of the Huntington's disease (HD) is intracellular inclusions containing a huntingtin (Htt) protein with an elongated polyglutamine tract. Aggregation of mutant Htt causes abnormal protein-protein interactions, and the functional dysregulation of aggregate-interacting proteins (AIPs) has been proposed as a pathomechanism of HD. Despite this, a molecular mechanism remains unknown how Htt aggregates sequester AIPs. We note an RNA-binding protein, TIA-1, as a model of AIPs containing a Q/N-rich sequence and suggest that in vitro and in vivo Htt fibrillar aggregates function as a structural template for inducing insoluble fibrillation of TIA-1. It is also plausible that such a cross-seeding activity of Htt aggregates represses the physiological function of TIA-1. We thus propose that Htt aggregates act as an intracellular hub for the cross-seeded fibrillation of Q/N-rich AIPs and that a cross-seeding reaction is a molecular origin to cause diverse pathologies in a polyglutamine disease.
亨廷顿舞蹈症(HD)的一个病理特征是细胞内包含有带有延长型聚谷氨酰胺序列的亨廷顿蛋白(Htt)的包涵体。突变型Htt的聚集会导致异常的蛋白质-蛋白质相互作用,并且聚集相互作用蛋白(AIPs)的功能失调被认为是HD的一种发病机制。尽管如此,Htt聚集体如何隔离AIPs的分子机制仍然未知。我们注意到一种RNA结合蛋白TIA-1,它作为一种含有富含Q/N序列的AIPs模型,并表明在体外和体内Htt纤维状聚集体作为诱导TIA-1不溶性纤维化的结构模板。Htt聚集体这样的交叉播种活性也可能抑制TIA-1的生理功能。因此,我们提出Htt聚集体作为富含Q/N的AIPs交叉播种纤维化作用的细胞内中心,并且交叉播种反应是在多聚谷氨酰胺疾病中导致多种病理状态的分子起源。