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Cytogenetic analysis of interphase cells using spectral imaging SIm technology

机译:利用光谱成像SIm技术进行间期细胞的细胞遗传学分析

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Abstract: Spectral Imaging (SIm) has dramatically improved our ability to localize and quantitatively analyze multiple nucleic acid targets such as chromosomes, genes and gene transcripts. Studies on metaphase cells such as `Spectral Karyotyping' are less complicated than interphase cell studies because the objects (chromosomes) are spatially separated and ratio- labeled probes can be used to uniquely stain each chromosome type. Our research, however, targets the extensive cytogenetic and phenotypic analysis of interphase cells. The complex organization of interphase chromatin and co- localization of gene transcripts (RNAs) in nuclear or cytoplasmic domains requires unique fluorochrome-labeling for each nucleic acid target. An increasing number of commercially available dyes for probe labeling and software to deconvolute partially overlapping emission spectra has helped to overcome most of these obstacles. This presentation summarizes our experience in analyzing numerical and structural alterations in various human cell types (leukocytes, amniocytes, blastomeres or solid tissue) as well as our approach to multi-gene expression profiling using SIm. Examples illustrate a wide spectrum of groundbreaking techniques for interphase cell analysis. We demonstrate how ten or more chromosomes can be scored in interphase nuclei or the relative level of expression of different transforming RNAs in tumor cells can be measured by SIm.!23
机译:摘要:光谱成像(SIm)极大地提高了我们对多种核酸靶标(例如染色体,基因和基因转录本)进行定位和定量分析的能力。诸如“光谱核型分析”之类的中期细胞研究要比相间细胞研究复杂,因为对象(染色体)在空间上是分开的,并且比率标记的探针可用于对每种染色体类型进行独特染色。然而,我们的研究针对间期细胞的广泛细胞遗传学和表型分析。相间染色质的复杂组织和基因转录本(RNA)在核或细胞质域中的共定位,需要对每个核酸靶标进行独特的荧光染料标记。越来越多的用于探针标记的市售染料和用于对部分重叠的发射光谱进行去卷积的软件,已帮助克服了大多数这些障碍。本演讲总结了我们在分析各种人类细胞类型(白细胞,羊膜细胞,卵裂球或实体组织)中的数字和结构变化方面的经验,以及我们使用SIm进行多基因表达谱分析的方法。实例说明了用于相间细胞分析的多种突破性技术。我们证明了如何在相间核中对10条或更多条染色体进行评分,或者可以通过SIm测量肿瘤细胞中不同转化RNA的相对表达水平!23

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