de Chiara C, Giannini C, Adinolfi S, de Boer J, Guida S, Ramos A, Jodice C, Kioussis D, Pastore A
National Institute for Medical Research, The Ridgeway, NW71AA London, UK.
FEBS Lett. 2003 Sep 11;551(1-3):107-12. doi: 10.1016/s0014-5793(03)00818-4.
Ataxin-1 (ATX1), a human protein responsible for spinocerebellar ataxia type 1 in humans, shares a region of homology, named AXH module, with the apparently unrelated transcription factor HBP1. Here, we describe the first characterisation of the AXH module in terms of its structural properties and stability. By producing protein constructs spanning the AXH modules of ATX1 and HBP1 and by comparing their properties, we have identified the minimal region sufficient for forming independently folded units (domains). Knowledge of the AXH domain boundaries allows us to map many of the interactions of ATX1 with other molecules onto the AXH module. We further show that the AXH of ATX1 is a dimerisation domain and is able to recognise RNA with the same nucleotide preference previously described for the full-length protein. AXH is therefore a novel protein-protein and RNA binding motif.
ataxin-1(ATX1)是一种导致人类1型脊髓小脑共济失调的蛋白质,它与看似不相关的转录因子HBP1共享一个名为AXH模块的同源区域。在此,我们首次描述了AXH模块的结构特性和稳定性。通过构建跨越ATX1和HBP1的AXH模块的蛋白质构建体并比较它们的特性,我们确定了足以形成独立折叠单元(结构域)的最小区域。了解AXH结构域边界使我们能够将ATX1与其他分子的许多相互作用映射到AXH模块上。我们进一步表明,ATX1的AXH是一个二聚化结构域,并且能够以与全长蛋白质先前描述的相同核苷酸偏好识别RNA。因此,AXH是一种新型的蛋白质-蛋白质和RNA结合基序。