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An oligonucleotide microarray for mouse imprinted genes profiling.

机译:用于小鼠印迹基因分析的寡核苷酸微阵列。

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Genomic imprinting is an epigenetic phenomenon unique to mammals that causes some genes to be expressed according to their parental origin. It results in developmental asymmetry in the function of the parental genomes. We describe here a method for the profiling of imprinted genes based on the development of a mouse imprinting microchip containing oligonucleotides corresponding to 493 genes, including most of the known imprinted genes (IG = 63), genes involved in epigenetic processes (EPI = 15), in metabolism (= 147), in obesity (= 10) and in neurotransmission (= 256) and housekeeping reference genes (= 2). This custom oligonucleotide microarray has been constructed to make data analysis and handling more manageable than pangenomic microarrays. As a proof of concept we present the differential expression of these 493 genes in different tissues (liver, placenta, embryo) of C57BL6/J mice fed different diets. Appropriate experimental strategies and statistical tools were defined at each step of the data analysis process with regard to the different sources of constraints. Data were confirmed by expression analyses based on quantitative real-time PCR. These oligochips should make it possible to increase our understanding of the involvement of imprinted genes in the timing of expression programs, tissue by tissue, stage by stage, in response to nutrients, lifestyles and other as yet unknown critical environmental factors in a variety of physiopathological situations, and in animals of different strains, ages and sexes. The use of oligonucleotides makes it possible to expand this microchip to include the increasing number of imprinted genes discovered.
机译:基因组印记是哺乳动物特有的表观遗传现象,可导致某些基因根据其亲本来源表达。这导致亲本基因组功能的发育不对称。我们在这里描述一种基于印迹基因芯片的开发方法,该方法基于小鼠印迹微芯片的开发,该芯片包含对应于493个基因的寡核苷酸,包括大多数已知的印迹基因(IG = 63),参与表观遗传过程的基因(EPI = 15) ,新陈代谢(= 147),肥胖症(= 10),神经传递(= 256)和管家参考基因(= 2)。这种定制的寡核苷酸微阵列已被构建为比泛基因组微阵列更易于处理数据分析和处理。作为概念验证,我们介绍了这493个基因在不同饮食喂养的C57BL6 / J小鼠的不同组织(肝脏,胎盘,胚胎)中的差异表达。在数据分析过程的每个步骤中,针对不同的约束源都定义了适当的实验策略和统计工具。通过基于定量实时PCR的表达分析确认数据。这些寡核苷酸芯片将使我们对印迹基因参与表达程序,组织,阶段,响应营养,生活方式和各种生理病理学中其他未知环境关键因素的时机参与的理解成为可能。情况以及不同品系,年龄和性别的动物。寡核苷酸的使用使得有可能扩展该微芯片以包括增加数量的发现的印迹基因。

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