Ko Dennis C, Jaslow Sarah L
Department of Molecular Genetics and Microbiology; School of Medicine; Duke University; Durham, NC USA; Department of Medicine and the Center for Human Genome Variation; School of Medicine; Duke University; Durham, NC USA.
Department of Molecular Genetics and Microbiology; School of Medicine; Duke University; Durham, NC USA.
Bioarchitecture. 2014 Mar-Apr;4(2):58-61. doi: 10.4161/bioa.28481. Epub 2014 Mar 11.
Microtubules play a central role in many essential cellular processes, including chromosome segregation, intracellular transport, and cell polarity. As these dynamic polymers are crucial components of eukaryotic cellular architecture, we were surprised by our recent discovery that a common human genetic difference leads to variation in microtubule stability in cells from different people. A single nucleotide polymorphism (SNP) near the TUBB6 gene, encoding class V β-tubulin, is associated with the expression level of this protein, which reduces microtubule stability at higher levels of expression. We discuss the novel cellular GWAS (genome-wide association study) platform that led to this discovery of natural, common variation in microtubule stability and the implications this finding may have for human health and disease, including cancer and neurological disorders. Furthermore, our generalizable approach provides a gateway for cell biologists to help interpret the functional consequences of human genetic variation.
微管在许多重要的细胞过程中发挥着核心作用,包括染色体分离、细胞内运输和细胞极性。由于这些动态聚合物是真核细胞结构的关键组成部分,我们最近发现一个常见的人类基因差异会导致不同人细胞中微管稳定性的变化,这让我们感到惊讶。编码V类β-微管蛋白的TUBB6基因附近的一个单核苷酸多态性(SNP)与该蛋白的表达水平相关,在较高表达水平时会降低微管稳定性。我们讨论了导致这一微管稳定性自然常见变异发现的新型细胞全基因组关联研究(GWAS)平台,以及这一发现可能对人类健康和疾病(包括癌症和神经疾病)产生的影响。此外,我们的通用方法为细胞生物学家帮助解释人类基因变异的功能后果提供了一条途径。