Laboratory of Chemical Biology and Signal Transduction, The Rockefeller University, 1230 York Ave., New York, NY, 10065, USA.
Department of Neurobiology, Care Sciences and Society, Division for Neurogeriatrics, Center for Alzheimer Research, Karolinska Institutet, 141 57, Huddinge, Sweden.
Sci Rep. 2017 Mar 15;7(1):190. doi: 10.1038/s41598-017-00250-4.
Recent reports show transcription preference for long genes in neuronal tissues compared with non-neuronal tissues, and a gene-length dependent change in expression in the neurodevelopmental disease Rett syndrome (RTT). Whether the gene-length dependent changes in expression seen in RTT might also be seen in neurodegenerative diseases is not yet known. However, a reasonable hypothesis is that similar effects might be seen in neurodegenerative diseases as well as in RTT since a common general feature of both illnesses involves progressive dysfunction of synapses. Here, we demonstrate a clear length-dependent gene misexpression in the most prevalent neurodegenerative disease, Alzheimer's disease. We show that the effect is associated with disease progression and can be attributed specifically to neurons. In particular, we observed gene length-dependent down regulation on the level of the whole tissue and gene length-dependent up regulation on the level of single cells. Our analysis shows that a gene-length effect on expression can be found in degenerative neurological illnesses, such as Alzheimer's disease. Additional investigation to elucidate the precise mechanism underlying gene-length dependent changes in expression is warranted.
最近的报告显示,与非神经元组织相比,神经元组织中转录对长基因具有偏好性,并且神经发育疾病雷特综合征(RTT)中的表达也存在基因长度依赖性变化。RTT 中观察到的表达的基因长度依赖性变化是否也可能出现在神经退行性疾病中尚不清楚。然而,一个合理的假设是,由于这两种疾病的一个共同特征都涉及突触的进行性功能障碍,因此类似的影响也可能出现在神经退行性疾病和 RTT 中。在这里,我们在最常见的神经退行性疾病阿尔茨海默病中证明了明显的长度依赖性基因表达错误。我们表明,这种效应与疾病进展有关,并且可以专门归因于神经元。特别是,我们观察到整个组织水平上的基因长度依赖性下调和单个细胞水平上的基因长度依赖性上调。我们的分析表明,表达的基因长度效应可以在退行性神经疾病中找到,如阿尔茨海默病。需要进一步研究以阐明表达的基因长度依赖性变化背后的确切机制。