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一种实时 PCR 方法,用于对 Na,K-ATPase 上变构性亲合力的心脏毒素甾体的突变体小鼠模型进行基因分型。

A real-time PCR method to genotype mutant mouse models with altered affinity for cardiotonic steroids on the Na,K-ATPase.

机构信息

Molecular Research Center, Cincinnati, OH, United States of America.

Department of Pharmacology and Systems Physiology, University of Cincinnati, Cincinnati, OH, United States of America.

出版信息

PLoS One. 2022 Apr 21;17(4):e0267348. doi: 10.1371/journal.pone.0267348. eCollection 2022.

Abstract

The highly conserved, cardiotonic steroid binding site (also termed ouabain binding site) on the primary α subunit of Na,K-ATPase plays a receptor signaling role in a range of vital cell processes and is a therapeutic target for human disease. Mouse lines with altered affinity for cardiotonic steroids on the α1 or α2 subunit isoform of Na,K-ATPase, without any change in pump activity, were developed by the late Jerry B Lingrel and are a valuable tool for studying its physiological roles and drug actions. In one model, the normally ouabain resistant α1 isoform was rendered sensitive to ouabain binding. In a second model, the normally sensitive α2 isoform was rendered resistant to ouabain binding. Additional useful models are obtained by mating these mice. To further advance their use, we developed a rapid, real-time PCR method that detects mutant alleles using specific primers and fluorescent probes. PCR is performed in fast mode with up to 15 samples processed in 40 min. The method was validated by Sanger sequencing using mice of known genotype, and by comparing results with a previous two-step method that used PCR amplification followed by gel electrophoresis. In addition, we clarified inconsistencies in published sequences, updated numbering to current reference sequences, and confirmed the continued presence of the mutations in the colony. It is expected that a wider availability of these models and a more efficient genotyping protocol will advance studies of the Na,K-ATPase and its cardiotonic steroid receptor.

摘要

钠钾 ATP 酶的主要 α 亚基上高度保守的、具有正性肌力作用的甾体结合位点(也称为哇巴因结合位点)在一系列重要的细胞过程中发挥受体信号作用,是人类疾病的治疗靶点。通过已故的 Jerry B. Lingrel 开发了改变钠钾 ATP 酶的 α1 或 α2 亚基同工型上的强心甾体亲和力而不改变泵活性的小鼠品系,这是研究其生理作用和药物作用的有价值工具。在一种模型中,通常对哇巴因具有抗性的 α1 同工型变得对哇巴因结合敏感。在第二种模型中,通常对哇巴因敏感的 α2 同工型变得对哇巴因结合具有抗性。通过交配这些小鼠可以获得其他有用的模型。为了进一步推进其使用,我们开发了一种快速、实时 PCR 方法,该方法使用特定的引物和荧光探针检测突变等位基因。PCR 以快速模式进行,最多可在 40 分钟内处理多达 15 个样本。该方法使用已知基因型的小鼠通过 Sanger 测序进行了验证,并通过与先前使用 PCR 扩增 followed 凝胶电泳的两步法进行了比较。此外,我们澄清了已发表序列中的不一致之处,将编号更新为当前参考序列,并确认了突变在该品系中的持续存在。预计这些模型的更广泛可用性和更有效的基因分型方案将推进钠钾 ATP 酶及其强心甾体受体的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d39/9022855/3283fb7d7931/pone.0267348.g001.jpg

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