Mitochondrial heteroplasmy profiling in single human oocytes by next-generation sequencing

被引:2
|
作者
Ancora, Massimo [1 ]
Orsini, Massimiliano [1 ]
Colosimo, Alessia [2 ]
Russo, Valentina [2 ]
Marcacci, Maurilia [1 ]
De Santo, Maria [3 ]
D'Aurora, Marco [4 ]
Stuppia, Liborio [4 ]
Gatta, Valentina [4 ]
Barboni, Barbara [2 ]
Camma, Cesare [1 ]
Mattioli, Mauro [1 ]
机构
[1] Ist Zooprofilatt Sperimentale Abruzzo & Molise G, Via Campo Boario, I-64100 Teramo, Italy
[2] Univ Teramo, Fac Biosci & Tecnol Agroalimentari & Ambientali, Teramo, Italy
[3] Casa Cura Privata Synergo Pierangeli, Chieti, Italy
[4] Univ G DAnnunzio, Dipartimento Sci Psicol Salute & Terr, Chieti, Italy
来源
MITOCHONDRIAL DNA PART B-RESOURCES | 2017年 / 2卷 / 02期
关键词
Heteroplasmic mutations; human oocyte; mitochondrial DNA; next-generation sequencing;
D O I
10.1080/23802359.2017.1365634
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Mitochondrial DNA (mtDNA) plays a key role in the development of a competent oocyte. Mutations of the mitochondrial genome lead to an altered energetic metabolism with negative effects on oocyte developmental competence. In this study, mtDNA heteroplasmy at an intra-oocyte level and between the different analyzed human oocytes (n = 12) was identified by a next-generation sequencing (NGS) protocol previously developed by this research group and submitted to GenBank. This method highlighted, in particular, variants in the genes involved in the respiratory chain providing a direct indication of the cell-specific damage within the mitochondrial genome as predictor of the oocyte quality.
引用
收藏
页码:542 / 543
页数:2
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