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ATXN2 是 N 端蛋白水解的靶标。

ATXN2 is a target of N-terminal proteolysis.

机构信息

Department of Neurobiology, University of Massachusetts Chan Medical School, Worcester, Massachusetts, United States of America.

Interdisciplinary Graduate Program, Morningside Graduate School of Biomedical Sciences, University of Massachusetts Chan Medical School, Worcester, Massachusetts, United States of America.

出版信息

PLoS One. 2023 Dec 21;18(12):e0296085. doi: 10.1371/journal.pone.0296085. eCollection 2023.

Abstract

Spinocerebellar ataxia 2 (SCA2) is a neurodegenerative disorder caused by the expansion of the poly-glutamine (polyQ) tract of Ataxin-2 (ATXN2). Other polyQ-containing proteins such as ATXN7 and huntingtin are associated with the development of neurodegenerative diseases when their N-terminal polyQ domains are expanded. Furthermore, they undergo proteolytic processing events that produce N-terminal fragments that include the polyQ stretch, which are implicated in pathogenesis. Interestingly, N-terminal ATXN2 fragments were reported in a brain extract from a SCA2 patient, but it is currently unknown whether an expanded polyQ domain contributes to ATXN2 proteolytic susceptibility. Here, we used transient expression in HEK293 cells to determine whether ATXN2 is a target for specific N-terminal proteolysis. We found that ATXN2 proteins with either normal or expanded polyQ stretches undergo proteolytic cleavage releasing an N-terminal polyQ-containing fragment. We identified a short amino acid sequence downstream of the polyQ domain that is necessary for N-terminal cleavage of full-length ATXN2 and sufficient to induce proteolysis of a heterologous protein. However, this sequence is not required for cleavage of a short ATXN2 isoform produced from an alternative start codon located just upstream of the CAG repeats encoding the polyQ domain. Our study extends our understanding of ATXN2 posttranslational regulation by revealing that this protein can be the target of specific proteolytic cleavage events releasing polyQ-containing products that are modulated by the N-terminal domain of ATXN2. N-terminal ATXN2 proteolysis of expanded polyQ domains might contribute to SCA2 pathology, as observed in other neurodegenerative disorders caused by polyQ domain expansion.

摘要

脊髓小脑共济失调 2 型(SCA2)是一种由 Ataxin-2(ATXN2)的多聚谷氨酰胺(polyQ)序列扩展引起的神经退行性疾病。其他含有 polyQ 的蛋白质,如 ATXN7 和 huntingtin,当其 N 端 polyQ 结构域扩展时,与神经退行性疾病的发展有关。此外,它们经历蛋白水解加工事件,产生包含 polyQ 延伸的 N 端片段,这些片段与发病机制有关。有趣的是,在 SCA2 患者的脑提取物中报道了 N 端 ATXN2 片段,但目前尚不清楚扩展的 polyQ 结构域是否有助于 ATXN2 的蛋白水解易感性。在这里,我们使用 HEK293 细胞中的瞬时表达来确定 ATXN2 是否是特定 N 端蛋白水解的靶标。我们发现,具有正常或扩展的 polyQ 延伸的 ATXN2 蛋白经历蛋白水解切割,释放包含 N 端 polyQ 的片段。我们鉴定了 polyQ 结构域下游的一个短氨基酸序列,该序列对于全长 ATXN2 的 N 端切割是必需的,并且足以诱导异源蛋白的蛋白水解。然而,该序列不是切割位于编码 polyQ 结构域的 CAG 重复上游的替代起始密码子产生的短 ATXN2 同工型所必需的。我们的研究通过揭示该蛋白可以成为特定蛋白水解切割事件的靶标,释放受 ATXN2 N 端结构域调节的含 polyQ 产物,从而扩展了我们对 ATXN2 翻译后调控的理解。扩展的 polyQ 结构域的 ATXN2 N 端蛋白水解可能导致 SCA2 病理学,正如其他由 polyQ 结构域扩展引起的神经退行性疾病中观察到的那样。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5caa/10735043/33cfc79f46d9/pone.0296085.g001.jpg

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