Chase Kayla A, Rosen Cherise, Rubin Leah H, Feiner Benjamin, Bodapati Anjuli S, Gin Hannah, Hu Edward, Sharma Rajiv P
The Psychiatric Institute, University of Illinois at Chicago, 1601 W. Taylor St., Chicago, IL 60612, USA.
The Psychiatric Institute, University of Illinois at Chicago, 1601 W. Taylor St., Chicago, IL 60612, USA; Jesse Brown Veterans Affairs Medical Center, 820 South Damen Avenue (M/C 151), Chicago, IL 60612, USA.
J Psychiatr Res. 2015 Jun;65:87-94. doi: 10.1016/j.jpsychires.2015.04.005. Epub 2015 Apr 18.
When compared to women, men have a higher incidence of schizophrenia, with increases in negative and cognitive symptoms, and an overall poorer disease course. Schizophrenia is conceptualized as a disorder of aberrant gene transcription and regulation. Thus, epigenetics, the study of environmentally induced changes in gene regulation, could advance our understanding of the molecular underpinnings of schizophrenia. Peripheral histone methyltransferase (HMT) mRNA levels have been previously shown to be significantly increased in patients with schizophrenia and correlate with symptomology. In this independent study, peripheral lymphocytes were extracted and clinical symptoms were measured on 74 participants, (40 patients with schizophrenia (19 women, 21 men) and 34 healthy individuals (19 women, 15 men)). HMT (G9α, SETDB1 and GLP) mRNA levels and their resulting histone modification H3K9me2 were measured with RT-PCR and ELISA respectively. Plasma estradiol levels were also measured via ELISA and correlated with HMT mRNA. Clinical symptoms were measured utilizing the Positive and Negative Syndrome Scale (PANSS) and the Heinrichs Carpenter Quality of Life Scale (QLS). The results indicate that men with schizophrenia expressed the highest levels of G9α, SETDB1 mRNA and H3K9me2 protein levels. Additionally, higher levels of symptom presentation and an overall poorer quality of life were correlated with higher HMT mRNA and H3K9me2 protein levels in a sex-dependent pattern. These data support the hypothesis of a sex-dependent restrictive epigenome contributing towards the etiology of schizophrenia. The histone methyltransferases measured here could be potential future therapeutic targets for small molecule pharmacology.
与女性相比,男性精神分裂症的发病率更高,阴性和认知症状增加,且疾病总体进程更差。精神分裂症被概念化为一种异常基因转录和调控的疾病。因此,表观遗传学,即对环境诱导的基因调控变化的研究,可能会增进我们对精神分裂症分子基础的理解。先前已表明,精神分裂症患者外周组蛋白甲基转移酶(HMT)的mRNA水平显著升高,且与症状学相关。在这项独立研究中,提取了74名参与者(40名精神分裂症患者(19名女性和21名男性)和34名健康个体(19名女性和15名男性))的外周淋巴细胞并测量了临床症状。分别用逆转录聚合酶链反应(RT-PCR)和酶联免疫吸附测定(ELISA)测量HMT(G9α、SETDB1和GLP)的mRNA水平及其产生的组蛋白修饰H3K9me2。还通过ELISA测量了血浆雌二醇水平,并将其与HMT的mRNA相关联。利用阳性和阴性症状量表(PANSS)和海因里希斯·卡彭特生活质量量表(QLS)测量临床症状。结果表明,患有精神分裂症的男性表达的G9α、SETDB1的mRNA水平以及H3K9me2蛋白水平最高。此外,更高水平的症状表现和总体较差的生活质量与更高的HMT mRNA和H3K9me2蛋白水平呈性别依赖性模式相关。这些数据支持了性别依赖性限制性表观基因组促成精神分裂症病因的假说。此处测量的组蛋白甲基转移酶可能是未来小分子药理学的潜在治疗靶点。