hPSCs的染色体质量控制:使用GenomeStudio进行SNP阵列分析的实用指南。

IF 4.6 2区 生物学 Q2 CELL BIOLOGY
Frontiers in Cell and Developmental Biology Pub Date : 2025-07-01 eCollection Date: 2025-01-01 DOI:10.3389/fcell.2025.1599923
Josephine Haake, Laura Steenpass
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引用次数: 0

摘要

人类多能干细胞(hPSCs)是临床前研究和疾病建模的重要工具。只有使用完全质量控制的人造血干细胞才能获得有效的结果,其中包括确保染色体稳定性。在重编程、基因编辑或维持培养过程中经常出现的染色体畸变会损害这些细胞在研究和治疗应用中的效用。虽然传统的g带仍然是一种有价值的全基因组分析方法,但其有限的分辨率需要补充的方法。SNP阵列分析提供了一种高分辨率的替代方案,提供了更详细的基因组概述。我们提出了一个实用和用户友好的指南,用于检测染色体畸变使用Illumina的GenomeStudio,提供一个易于遵循的协议,以简化质量控制工作流程的研究人员最少的生物信息学专业知识。虽然用于hPSC质量控制的SNP阵列分析并不新颖,但本逐步指南强调了关键的质量控制指标、阈值和值,简化了流程,使其更容易获得,更有效,更广泛地采用。在32个hPSC中,我们发现了9个染色体畸变,包括经常报道的20q11.21的增加,这是hPSC培养中常见的异常。我们日常实践的例子强调了监测染色体完整性的重要性。本指南可作为标准化和加强质量控制过程的实用资源,确保研究和临床应用的人造血干细胞基因组稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chromosomal quality control in hPSCs: A practical guide to SNP array analysis with GenomeStudio.

Human pluripotent stem cells (hPSCs) are important tools in preclinical research and disease modeling. Valid results can only be obtained using thoroughly quality-controlled hPSCs, which includes ensuring chromosomal stability. Chromosomal aberrations, which frequently arise during reprogramming, gene editing, or maintenance cultivation, can compromise the utility of these cells in research and therapeutic applications. Although traditional G-banding remains a valuable genome-wide analysis method, its limited resolution necessitates complementary approaches. SNP array analysis offers a high-resolution alternative, providing a more detailed genomic overview. We present a practical and user-friendly guide for detecting chromosomal aberrations using Illumina's GenomeStudio, offering an easy-to-follow protocol to simplify quality control workflows for researchers with minimal bioinformatics expertise. Although SNP array analysis for hPSC quality control is not novel, this step-by-step guide highlights critical quality control metrics, thresholds, and values, streamlining the process to make it more accessible and efficient for broader adoption. In 32 hPSCs, we identified chromosomal aberrations in nine, including the frequently reported gain of 20q11.21-a common anomaly in hPSC cultures. Examples from our routine practices underscore the importance of monitoring chromosomal integrity. This guide serves as a practical resource for standardizing and enhancing quality control processes, ensuring the genomic stability of hPSCs for research and clinical applications.

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来源期刊
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
9.70
自引率
3.60%
发文量
2531
审稿时长
12 weeks
期刊介绍: Frontiers in Cell and Developmental Biology is a broad-scope, interdisciplinary open-access journal, focusing on the fundamental processes of life, led by Prof Amanda Fisher and supported by a geographically diverse, high-quality editorial board. The journal welcomes submissions on a wide spectrum of cell and developmental biology, covering intracellular and extracellular dynamics, with sections focusing on signaling, adhesion, migration, cell death and survival and membrane trafficking. Additionally, the journal offers sections dedicated to the cutting edge of fundamental and translational research in molecular medicine and stem cell biology. With a collaborative, rigorous and transparent peer-review, the journal produces the highest scientific quality in both fundamental and applied research, and advanced article level metrics measure the real-time impact and influence of each publication.
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