Świtońska Karolina, Szlachcic Wojciech J, Handschuh Luiza, Wojciechowski Paweł, Marczak Łukasz, Stelmaszczuk Michał, Figlerowicz Marek, Figiel Maciej
Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznań, Poland.
Institute of Computing Science, Poznan University of Technology, Poznań, Poland.
Front Cell Neurosci. 2019 Jan 18;12:528. doi: 10.3389/fncel.2018.00528. eCollection 2018.
In Huntington disease (HD) subtle symptoms in patients may occur years or even decades prior to diagnosis. HD changes at a molecular level may begin as early as in cells that are non-lineage committed such as stem cells or HD patients induced pluripotent stem cells (iPSCs) offering opportunity to enhance the understanding of the HD pathogenesis. In addition, juvenile HD non-linage committed cells were previously not directly investigated in detail by RNA-seq. In the present manuscript, we define the early HD and juvenile HD transcriptional alterations using 6 human HD iPS cell lines from two patients, one with 71 CAGs and one with 109 CAG repeats. We identified 107 (6 HD lines), 198 (3 HD71Q lines) and 217 (3 HD109Q lines) significantly dysregulated mRNAs in each comparison group. The analyses showed that many of dysregulated transcripts in HD109Q iPSC lines are involved in DNA damage response and apoptosis, such as CCND1, CDKN1A, TP53, BAX, TNFRSF10B, TNFRSF10C, TNFRSF10D, DDB2, PLCB1, PRKCQ, HSH2D, ZMAT3, PLK2, and RPS27L. Most of them were identified as downregulated and their proteins are direct interactors with TP53. HTT probably alters the level of several TP53 interactors influencing apoptosis. This may lead to accumulation of an excessive number of progenitor cells and potential disruption of cell differentiation and production of mature neurons. In addition, HTT effects on cell polarization also demonstrated in the analysis may result in a generation of incorrect progenitors. Bioinformatics analysis of transcripts dysregulated in HD71Q iPSC lines showed that several of them act as transcription regulators during the early multicellular stages of development, such as ZFP57, PIWIL2, HIST1H3C, and HIST1H2BB. Significant upregulation of most of these transcripts may lead to a global increase in expression level of genes involved in pathways critical for embryogenesis and early neural development. In addition, MS analysis revealed altered levels of TP53 and ZFP30 proteins reflecting the functional significance of dysregulated mRNA levels of these proteins which were associated with apoptosis and DNA binding. Our finding very well corresponds to the fact that mutation in the HTT gene may cause precocious neurogenesis and identifies pathways likely disrupted during development.
在亨廷顿舞蹈症(HD)中,患者的细微症状可能在诊断前数年甚至数十年就已出现。HD在分子水平上的变化可能早在非谱系定向细胞(如干细胞或HD患者诱导多能干细胞(iPSC))中就已开始,这为深入了解HD发病机制提供了契机。此外,此前尚未通过RNA测序对青少年HD非谱系定向细胞进行直接详细研究。在本论文中,我们使用来自两名患者的6个人类HD iPS细胞系(一名患者有71个CAG重复序列,另一名患者有109个CAG重复序列)来定义早期HD和青少年HD的转录改变。我们在每个比较组中分别鉴定出107个(6个HD细胞系)、198个(3个HD71Q细胞系)和217个(3个HD109Q细胞系)显著失调的mRNA。分析表明,HD109Q iPSC细胞系中许多失调的转录本参与DNA损伤反应和细胞凋亡,如CCND1、CDKN1A、TP53、BAX、TNFRSF10B、TNFRSF10C、TNFRSF10D、DDB2、PLCB1、PRKCQ、HSH2D、ZMAT3、PLK2和RPS27L。其中大多数被鉴定为下调,且它们的蛋白质是TP53的直接相互作用分子。HTT可能会改变几种与TP53相互作用的分子的水平,从而影响细胞凋亡。这可能导致祖细胞数量过多积累,并可能破坏细胞分化和成熟神经元的产生。此外,分析中还表明HTT对细胞极化的影响可能导致产生错误的祖细胞。对HD71Q iPSC细胞系中失调转录本的生物信息学分析表明,其中一些在发育的早期多细胞阶段作为转录调节因子发挥作用,如ZFP57、PIWIL2、HIST1H3C和HIST1H2BB。这些转录本中的大多数显著上调可能导致参与胚胎发生和早期神经发育关键途径的基因表达水平整体升高。此外,质谱分析显示TP53和ZFP30蛋白水平发生改变,这反映了与细胞凋亡和DNA结合相关的这些蛋白失调的mRNA水平的功能意义。我们的发现与HTT基因突变可能导致过早神经发生这一事实非常吻合,并确定了发育过程中可能被破坏的途径。