用于细胞遗传学研究的禽类胚胎染色体直接制备方法:快速、简便、廉价

S. A. Barcellos, M. S. de Souza, Victoria Tura, Larissa Rodrigues Pereira, Rafael Kretschmer, R. J. Gunski, A. D. Garnero
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引用次数: 3

摘要

禽细胞培养被广泛应用于细胞遗传学研究,其改进越来越多地允许产生高质量的染色体,这对进行经典和分子细胞遗传学研究至关重要。在这些方法中,有两种主要类型:成纤维细胞和骨髓培养。尽管成纤维细胞培养成本高且复杂,但由于所产生中期的质量,它被认为是一种优越的方法。短期骨髓培养提供了更多浓缩的染色体,但仍然更快更容易。为了寻找一种更快、更便宜的方法来制备中期而不损失质量,本工作开发了一种新的、广泛适用的鸟类染色体制备方案。采集了来自不同科的21个鸟类胚胎:冰蝶科、Columbidae、Furnaridae、Estrididae、Throupidae、Troglodytidae和Ardeidae。该方案以改良成纤维细胞培养和骨髓培养相结合为基础,综合了两者的优点。结果表明,所有物种都表现出良好的有丝分裂指数和高质量的染色体。总的来说,考虑到大多数成纤维细胞培养至少需要3天,而且通常需要更长的时间,将该方案应用于鸟类细胞遗传学可以优化时间。然而,我们的方案可以在3小时内完成,试剂和设备的成本大大降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Direct Chromosome Preparation Method in Avian Embryos for Cytogenetic Studies: Quick, Easy and Cheap
Avian cell culture is widely applied for cytogenetic studies, the improvement of which increasingly allows for the production of high-quality chromosomes, essential to perform both classical and molecular cytogenetic studies. Among these approaches, there are two main types: fibroblast and bone marrow culture. Despite its high cost and complexity, fibroblast culture is considered the superior approach due to the quality of the metaphases produced. Short-term bone marrow cultivation provides more condensed chromosomes but nonetheless is quicker and easier. In the search for a quicker, cheaper way to prepare metaphases without losing quality, the present work developed a novel, widely applicable protocol for avian chromosome preparation. Twenty-one bird embryos from distinct families were sampled: Icteridae, Columbidae, Furnariidae, Estrildidae, Thraupidae, Troglodytidae and Ardeidae. The protocol was based on a combination of modified fibroblast culture and bone marrow cultivation, taking the advantages of both. The results show that all species consistently presented good mitotic indexes and high-quality chromosomes. Overall, the application of this protocol for bird cytogenetics can optimize the time, considering that most fibroblast cultures take at least 3 days and often much longer. However, our protocol can be performed in 3 h with a much-reduced cost of reagents and equipment.
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