Department of Neurology, University of Michigan-Ann Arbor, Ann Arbor, United States.
Neuroscience Graduate Program, University of Michigan-Ann Arbor, Ann Arbor, United States.
Elife. 2023 Mar 20;12:e84043. doi: 10.7554/eLife.84043.
Over a third of the human genome is comprised of repetitive sequences, including more than a million short tandem repeats (STRs). While studies of the pathologic consequences of repeat expansions that cause syndromic human diseases are extensive, the potential native functions of STRs are often ignored. Here, we summarize a growing body of research into the normal biological functions for repetitive elements across the genome, with a particular focus on the roles of STRs in regulating gene expression. We propose reconceptualizing the pathogenic consequences of repeat expansions as aberrancies in normal gene regulation. From this altered viewpoint, we predict that future work will reveal broader roles for STRs in neuronal function and as risk alleles for more common human neurological diseases.
人类基因组的三分之一以上由重复序列组成,其中包括超过 100 万个短串联重复序列 (STRs)。虽然对导致综合征的人类疾病的重复扩展的病理后果的研究已经很广泛,但 STRs 的潜在自然功能往往被忽视。在这里,我们总结了越来越多的关于基因组中重复元件的正常生物学功能的研究,特别关注 STRs 在调节基因表达中的作用。我们提出将重复扩展的致病后果重新概念化为正常基因调控的异常。从这个改变的角度来看,我们预测未来的工作将揭示 STRs 在神经元功能中的更广泛作用,并作为更常见的人类神经疾病的风险等位基因。