Gladstone Institute of Data Science and Biotechnology, San Francisco, California, USA; email:
Department of Epidemiology and Biostatistics, University of California, San Francisco, California, USA.
Annu Rev Genet. 2022 Nov 30;56:423-439. doi: 10.1146/annurev-genet-071819-103933. Epub 2022 Sep 7.
Human accelerated regions (HARs) are the fastest-evolving sequences in the human genome. When HARs were discovered in 2006, their function was mysterious due to scant annotation of the noncoding genome. Diverse technologies, from transgenic animals to machine learning, have consistently shown that HARs function as gene regulatory enhancers with significant enrichment in neurodevelopment. It is now possible to quantitatively measure the enhancer activity of thousands of HARs in parallel and model how each nucleotide contributes to gene expression. These strategies have revealed that many human HAR sequences function differently than their chimpanzee orthologs, though individual nucleotide changes in the same HAR may have opposite effects, consistent with compensatory substitutions. To fully evaluate the role of HARs in human evolution, it will be necessary to experimentally and computationally dissect them across more cell types and developmental stages.
人类加速区(HARs)是人类基因组中进化最快的序列。2006 年发现 HARs 时,由于对非编码基因组的注释很少,其功能尚不清楚。从转基因动物到机器学习的各种技术都一致表明,HARs 作为基因调控增强子发挥作用,在神经发育中富集显著。现在已经可以定量测量数千个 HAR 的增强子活性,并对每个核苷酸如何促进基因表达进行建模。这些策略表明,许多人类 HAR 序列的功能不同于它们的黑猩猩同源物,尽管同一 HAR 中的单个核苷酸变化可能具有相反的作用,这与补偿性替换一致。要全面评估 HARs 在人类进化中的作用,有必要在更多的细胞类型和发育阶段进行实验和计算剖析。