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果蝇HtrA2对细胞凋亡并非必需,但在PINK1下游发挥作用,且独立于Parkin。

Drosophila HtrA2 is dispensable for apoptosis but acts downstream of PINK1 independently from Parkin.

作者信息

Tain L S, Chowdhury R B, Tao R N, Plun-Favreau H, Moisoi N, Martins L M, Downward J, Whitworth A J, Tapon N

机构信息

MRC Centre for Developmental and Biomedical Genetics, University of Sheffield, Sheffield, UK.

出版信息

Cell Death Differ. 2009 Aug;16(8):1118-25. doi: 10.1038/cdd.2009.23. Epub 2009 Mar 13.

Abstract

High temperature requirement A2 (HtrA2/Omi) is a mitochondrial protease that exhibits proapoptotic and cell-protective properties and has been linked to Parkinson's disease (PD). Impaired mitochondrial function is a common trait in PD patients, and is likely to play a significant role in pathogenesis of parkinsonism, but the molecular mechanisms remain poorly understood. Genetic studies in Drosophila have provided valuable insight into the function of other PD-linked genes, in particular PINK1 and parkin, and their role in maintaining mitochondrial integrity. Recently, HtrA2 was shown to be phosphorylated in a PINK1-dependent manner, suggesting it might act in the PINK1 pathway. Here, we describe the characterization of mutations in Drosophila HtrA2, and genetic analysis of its function with PINK1 and parkin. Interestingly, we find HtrA2 appears to be dispensable for developmental or stress-induced apoptosis. In addition, we found HtrA2 mutants share some phenotypic similarities with parkin and PINK1 mutants, suggesting that it may function in maintaining mitochondrial integrity. Our genetic interaction studies, including analysis of double-mutant combinations and epistasis experiments, suggest HtrA2 acts downstream of PINK1 but in a pathway parallel to Parkin.

摘要

高温需求蛋白A2(HtrA2/Omi)是一种线粒体蛋白酶,具有促凋亡和细胞保护特性,且与帕金森病(PD)有关。线粒体功能受损是PD患者的一个共同特征,可能在帕金森综合征的发病机制中起重要作用,但分子机制仍知之甚少。果蝇的遗传学研究为其他与PD相关基因的功能,特别是PINK1和parkin的功能及其在维持线粒体完整性中的作用提供了有价值的见解。最近,HtrA2被证明以PINK1依赖的方式磷酸化,这表明它可能在PINK1途径中起作用。在这里,我们描述了果蝇HtrA2突变的特征,以及对其与PINK1和parkin功能的遗传学分析。有趣的是,我们发现HtrA2对于发育性或应激诱导的凋亡似乎是可有可无的。此外,我们发现HtrA2突变体与parkin和PINK1突变体有一些表型相似性,这表明它可能在维持线粒体完整性中发挥作用。我们的遗传相互作用研究,包括双突变组合分析和上位性实验,表明HtrA2在PINK1下游起作用,但在与Parkin平行的途径中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27d0/2711053/5a41c04339a8/ukmss-3969-f0001.jpg

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