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Quantification of Neurospora crassa mitochondrial DNA using quantitative real-time PCR
被引:2
|作者:
Monteiro, J.
[1
,2
]
Videira, A.
[2
,3
,4
]
Pereira, F.
[5
]
机构:
[1] Univ Porto, Ctr Interdisciplinar Invest Marinha & Ambiental C, Porto, Portugal
[2] Univ Porto, ICBAS Inst Ciencias Biomed Abel Salazar, Porto, Portugal
[3] Univ Porto, IBMC Inst Biol Mol & Celular, Porto, Portugal
[4] Univ Porto, I3S Inst Invest & Inovacao Saude, Porto, Portugal
[5] Univ Porto UPTEC, Sci & Technol Pk, IDENTIFICA, Rua Alfredo Allen 455-461, Porto, Portugal
关键词:
DNA polymorphism;
DNA quantitation;
filamentous fungi;
mitochondria isolation;
mitochondrial DNA;
mtDNA quantification;
Neurospora crassa;
qPCR;
COPY NUMBER;
GENOME SEQUENCE;
GENETIC-CONTROL;
CELL-DEATH;
EXPRESSION;
MODEL;
D O I:
10.1111/lam.13294
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
The filamentous fungus Neurospora crassa is a popular model organism used in a wide range of biochemical and genetic studies and vastly used in mitochondrial research. Despite the relevance of mitochondria in N. crassa biology, no method for quantification of mitochondrial DNA (mtDNA) is currently available. Quantitative real-time PCR (qPCR) is a powerful tool, with a wide range of applications, and has been used for the quantification of nucleic acids in humans and a few other species. Here we present a new qPCR assay for relative quantification of N. crassa mtDNA. Three sets of qPCR primers targeting different regions of the mitochondrial genome were tested for mtDNA quantification. The qPCR was successfully validated in N. crassa strains from different geographical locations, representing the vast genetic diversity of this species, and knockout mutant strains. Moreover the assay proved to be efficient in templates with varied amounts of mitochondria, obtained through different DNA extraction methods. The qPCR performed well in all tested samples revealing a higher amount of mtDNA than nuclear DNA in all cases. This technique will facilitate the characterization of mtDNA of N. crassa in future studies and can be used as a tool to validate methods of mitochondria isolation.
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页码:171 / 178
页数:8
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