人肝组织和HepG2细胞系细胞色素P450基因mRNA剪接变异的纳米孔测序分析

IF 0.6 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
K. A. Deynichenko, K. G. Ptitsyn, S. P. Radko, L. K. Kurbatov, I. V. Vakhrushev, I. V. Buromski, S. S. Markin, A. I. Archakov, A. V. Lisitsa, E. A. Ponomarenko
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引用次数: 1

摘要

采用纳米孔测序方法对3个供体和HepG2细胞系的肝组织样本进行细胞色素P450转录本分析。研究表明,使用MinION纳米孔测序仪(Oxford nanopore Technologies)对mRNA进行直接测序,可以获得细胞色素P450超家族基因的转录本(及其剪接变体)的定量图谱,这些基因编码的亚型参与大多数(~80%)药物的代谢。不同供体的剪接变异谱差异很大。细胞色素P450基因在HepG2细胞系中转录水平的表达明显弱于正常肝组织。这限制了直接mRNA纳米孔测序研究HepG2细胞中细胞色素P450转录物选择性剪接的能力。在人肝组织和HepG2细胞中,细胞色素P450基因在转录水平上的定量和定性表达谱都存在显著差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Splice Variants of mRNA of Cytochrome P450 Genes: Analysis by the Nanopore Sequencing Method in Human Liver Tissue and HepG2 Cell Line

Splice Variants of mRNA of Cytochrome P450 Genes: Analysis by the Nanopore Sequencing Method in Human Liver Tissue and HepG2 Cell Line

The analysis of cytochrome P450 transcripts was carried out by the nanopore sequencing in liver tissue samples of three donors and HepG2 line cells. It was demonstrated that direct mRNA sequencing with a MinION nanopore sequencer (Oxford Nanopore Technologies) makes it possible to obtain quantitative profiles for transcripts (and their splice variants) of cytochrome P450 superfamily genes encoding isoforms involved in metabolism of the majority (~80%) of drugs. The splice variant profiles substantially differ for donors. The cytochrome P450 gene expression at the transcript level is significantly weaker in cells of the HepG2 line compared with that in the normal liver tissue. This limits the capability of the direct mRNA nanopore sequencing for studying alternative splicing of cytochrome P450 transcripts in HepG2 cells. Both quantitative and qualitative profiles of the cytochrome P450 gene expression at the transcript level notably differ in human liver tissue and HepG2 cells.

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来源期刊
CiteScore
1.10
自引率
0.00%
发文量
31
期刊介绍: Biochemistry (Moscow), Supplement Series B: Biomedical Chemistry   covers all major aspects of biomedical chemistry and related areas, including proteomics and molecular biology of (patho)physiological processes, biochemistry, neurochemistry, immunochemistry and clinical chemistry, bioinformatics, gene therapy, drug design and delivery, biochemical pharmacology, introduction and advertisement of new (biochemical) methods into experimental and clinical medicine. The journal also publishes review articles. All issues of the journal usually contain solicited reviews.
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