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甘油醛-3-磷酸脱氢酶假基因与猫基因组DNA当量的定量分析

GAPDH Pseudogenes and the Quantification of Feline Genomic DNA Equivalents.

作者信息

Helfer-Hungerbuehler A Katrin, Widmer Stefan, Hofmann-Lehmann Regina

机构信息

Clinical Laboratory, Vetsuisse Faculty, University of Zurich, Winterthurerstrasse 260, 8057 Zurich, Switzerland.

出版信息

Mol Biol Int. 2013;2013:587680. doi: 10.1155/2013/587680. Epub 2013 Apr 28.

Abstract

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.

摘要

定量实时聚合酶链反应(qPCR)被广泛用于检测和定量核酸靶标。为了确定细胞拷贝数和基因组当量,需要一个在基因组中以确定数量存在的合适参考基因,最好是作为单拷贝基因。对于大多数生物,已报道有可变数量的甘油醛-3-磷酸脱氢酶(GAPDH)假基因。然而,有人提出猫基因组中存在单拷贝的GAPDH假基因,因此GAPDH检测可用于定量猫基因组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,并提供一种合适的替代qPCR系统用于定量猫细胞拷贝数和基因组当量。生物信息学和测序结果表明,猫基因组中存在的不是一个而是几个密切相关的GAPDH样序列。因此,我们鉴定、开发、优化并验证了一种使用猫白蛋白(fALB)的替代参考基因检测方法。我们的数据强调,除了GAPDH假基因外,还需要一个替代参考基因来标准化gDNA水平。我们建议在未来的研究中使用fALB qPCR检测方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf0a/3655645/f5c9006a3999/MBI2013-587680.001.jpg

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