Aguilar Robin, Camplisson Conor K, Lin Qiaoyi, Miga Karen H, Noble William S, Beliveau Brian J
Department of Genome Sciences, University of Washington, Seattle, WA, USA.
Department of Biomolecular Engineering, University of California Santa Cruz, Santa Cruz, CA, USA.
bioRxiv. 2023 Mar 7:2023.03.06.530899. doi: 10.1101/2023.03.06.530899.
Fluorescent hybridization (FISH) is a powerful method for the targeted visualization of nucleic acids in their native contexts. Recent technological advances have leveraged computationally designed oligonucleotide (oligo) probes to interrogate >100 distinct targets in the same sample, pushing the boundaries of FISH-based assays. However, even in the most highly multiplexed experiments, repetitive DNA regions are typically not included as targets, as the computational design of specific probes against such regions presents significant technical challenges. Consequently, many open questions remain about the organization and function of highly repetitive sequences. Here, we introduce Tigerfish, a software tool for the genome-scale design of oligo probes against repetitive DNA intervals. We showcase Tigerfish by designing a panel of 24 interval-specific repeat probes specific to each of the 24 human chromosomes and imaging this panel on metaphase spreads and in interphase nuclei. Tigerfish extends the powerful toolkit of oligo-based FISH to highly repetitive DNA.
荧光杂交(FISH)是一种在核酸天然环境中对其进行靶向可视化的强大方法。最近的技术进步利用了通过计算设计的寡核苷酸(oligo)探针,能够在同一样本中检测超过100个不同的靶点,拓展了基于FISH检测的边界。然而,即使在最高度多重化的实验中,重复DNA区域通常也不被作为靶点,因为针对此类区域设计特异性探针存在重大技术挑战。因此,关于高度重复序列的组织和功能仍存在许多悬而未决的问题。在此,我们介绍Tigerfish,一种针对重复DNA区间进行全基因组规模寡核苷酸探针设计的软件工具。我们通过设计一组针对24条人类染色体中每条染色体的24个区间特异性重复探针,并在中期染色体铺展和间期细胞核中对该组探针进行成像,展示了Tigerfish的功能。Tigerfish将基于寡核苷酸的FISH强大工具包扩展到了高度重复的DNA。