GAPDH假基因和猫基因组DNA等同物的定量。

Molecular biology international Pub Date : 2013-01-01 Epub Date: 2013-04-28 DOI:10.1155/2013/587680
A Katrin Helfer-Hungerbuehler, Stefan Widmer, Regina Hofmann-Lehmann
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引用次数: 18

摘要

实时荧光定量PCR (Quantitative real-time PCR, qPCR)广泛用于核酸靶点的检测和定量。为了确定细胞拷贝数和基因组等效物,需要在基因组中以确定数量存在的合适的参考基因,优选为单拷贝基因。对于大多数生物体,已经报道了可变数量的甘油醛-3-磷酸脱氢酶(GAPDH)假基因。然而,有人认为,GAPDH假基因的单拷贝存在于猫的基因组中,因此,GAPDH测定可用于量化猫的基因组DNA (gDNA)。本研究的目的是确定猫基因组中是否存在一个或多个GAPDH假基因,并提供一种合适的qPCR系统来定量猫细胞拷贝数和基因组当量。生物信息学和测序结果显示,猫基因组中存在不止一个,而是几个密切相关的gapdh样序列。因此,我们确定、开发、优化并验证了一种使用猫白蛋白(fALB)的替代参比基因测定。我们的数据强调需要一个替代的参考基因,除了GAPDH假基因,为gDNA水平的正常化。我们建议在未来的研究中使用fALB qPCR检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

GAPDH Pseudogenes and the Quantification of Feline Genomic DNA Equivalents.

GAPDH Pseudogenes and the Quantification of Feline Genomic DNA Equivalents.

Quantitative real-time PCR (qPCR) is broadly used to detect and quantify nucleic acid targets. In order to determine cell copy number and genome equivalents, a suitable reference gene that is present in a defined number in the genome is needed, preferably as a single copy gene. For most organisms, a variable number of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) pseudogenes have been reported. However, it has been suggested that a single-copy of the GAPDH pseudogene is present in the feline genome and that a GAPDH assay can therefore be used to quantify feline genomic DNA (gDNA). The aim of this study was to determine whether one or more GAPDH pseudogenes are present in the feline genome and to provide a suitable alternative qPCR system for the quantification of feline cell copy number and genome equivalents. Bioinformatics and sequencing results revealed that not just one but several closely related GAPDH-like sequences were present in the cat genome. We thus identified, developed, optimized, and validated an alternative reference gene assay using feline albumin (fALB). Our data emphasize the need for an alternative reference gene, apart from the GAPDH pseudogene, for the normalization of gDNA levels. We recommend using the fALB qPCR assay for future studies.

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