CATS:在临床相关背景下用于自动比较Cas9核酸酶活性的生物信息学工具。

IF 4.4 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Frontiers in genome editing Pub Date : 2025-07-24 eCollection Date: 2025-01-01 DOI:10.3389/fgeed.2025.1571023
Ettore Rocchi, Federico Magnani, Gastone Castellani, Antonio Carusillo, Martina Tarozzi
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引用次数: 0

摘要

随着基因工程师可用的Cas9核酸酶数量的不断增加,为给定应用选择最合适的Cas9核酸酶可能具有挑战性。一个主要的复杂性来自于每个Cas9变体不同的原间隔邻近基序(PAM)序列要求,这使得直接比较变得困难。为了确保公平的比较,确定不受所选目标的自然遗传景观影响的共同目标位点是至关重要的。方法:为了解决这一挑战,我们开发了一种新的生物信息学工具CATS(比较Cas9活性的靶标叠加)。CATS可以自动检测不同Cas9核酸酶之间重叠的PAM序列,并识别等位基因特异性靶标,特别是那些由致病性突变引起的靶标。CATS的关键参数之一是PAM位点的接近性,这有助于最小化序列组成偏差。该工具整合了来自不断更新的来源的数据,并包括ClinVar信息,以促进靶向致病突变。结果:CATS显著减少了CRISPR/Cas9实验设计所需的时间和精力。它简化了不同PAM需求的Cas9核酸酶的比较,使研究人员能够为其特定的靶标选择最合适的核酸酶。该工具的自动化、速度和用户友好的界面使研究人员无论其计算专业知识如何都可以使用它。讨论:通过识别重叠的PAMs和等位基因特异性靶点,CATS支持在研究和临床环境中实现基于cas9的应用。它结合遗传变异的能力使得它在设计治疗方法时特别有用,这种方法可以选择性地针对突变的等位基因,同时保留健康的等位基因。最终,CATS有助于开发更有效和精确的基因疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

CATS: a bioinformatic tool for automated Cas9 nucleases activity comparison in clinically relevant contexts.

CATS: a bioinformatic tool for automated Cas9 nucleases activity comparison in clinically relevant contexts.

CATS: a bioinformatic tool for automated Cas9 nucleases activity comparison in clinically relevant contexts.

CATS: a bioinformatic tool for automated Cas9 nucleases activity comparison in clinically relevant contexts.

CATS: a bioinformatic tool for automated Cas9 nucleases activity comparison in clinically relevant contexts.

CATS: a bioinformatic tool for automated Cas9 nucleases activity comparison in clinically relevant contexts.

CATS: a bioinformatic tool for automated Cas9 nucleases activity comparison in clinically relevant contexts.

Introduction: With the growing number of Cas9 nucleases available to genetic engineers, selecting the most suitable one for a given application can be challenging. A major complication arises from the differing protospacer adjacent motif (PAM) sequence requirements of each Cas9 variant, which makes direct comparisons difficult. To ensure a fair comparison, it is essential to identify common target sites that are not biased by the natural genetic landscape of the chosen target.

Methods: To address this challenge, we developed CATS (Comparing Cas9 Activities by Target Superimposition), a novel bioinformatic tool. CATS automates the detection of overlapping PAM sequences across different Cas9 nucleases and identifies allele-specific targets, particularly those arising from pathogenic mutations. One of the key parameters in CATS is the proximity of PAM sites, which helps minimize sequence composition bias. The tool integrates data from continuously updated sources and includes ClinVar information to facilitate the targeting of disease-causing mutations.

Results: CATS significantly reduces the time and effort required for CRISPR/Cas9 experimental design. It streamlines the comparison of Cas9 nucleases with different PAM requirements, enabling researchers to select the most appropriate nuclease for their specific target. The tool's automation, speed, and user-friendly interface make it accessible to researchers regardless of their computational expertise.

Discussion: By enabling the identification of overlapping PAMs and allele-specific targets, CATS supports the implementation of Cas9-based applications in both research and clinical settings. Its ability to incorporate genetic variants makes it particularly useful for designing therapeutic approaches that selectively target mutated alleles while sparing healthy ones. Ultimately, CATS contributes to the development of more effective and precise genetic therapies.

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CiteScore
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