Amplification of DNA sequences in polar bodies from human oocytes for diagnosis of mitochondrial disease

被引:15
作者
Briggs, DA
Power, NJ
Lamb, V
Rutherford, AJ
Gosden, RG
机构
[1] Univ Leeds, Div Obstet & Gynaecol, Leeds, W Yorkshire, England
[2] Leeds Gen Infirm, Leeds, W Yorkshire, England
关键词
D O I
10.1016/S0140-6736(00)02171-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
When a preovulatory oocyte reinitiates meiosis, it sheds a cytoplasmic fragment containing mitochondria and redundant set of chromosomes. We have detected DNA sequences from both the mitochondrial and nuclear genomes in polar bodies from unfertilised human oocytes, demonstrating the feasibility of diagnosing mitochondrial diseases before conception.
引用
收藏
页码:1520 / 1521
页数:2
相关论文
共 4 条
[1]   Skewed segregation of the mtDNA nt 8993 (T->G) mutation in human oocytes [J].
Blok, RB ;
Gook, DA ;
Thorburn, DR ;
Dahl, HHM .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 60 (06) :1495-1501
[2]  
HANDYSIDE AH, 1989, LANCET, V1, P347
[3]   Tissue-specific selection for different mtDNA genotypes in heteroplasmic mice [J].
Jenuth, JP ;
Peterson, AC ;
Shoubridge, EA .
NATURE GENETICS, 1997, 16 (01) :93-95
[4]   Preimplantation diagnosis of single gene disorders by two-step oocyte genetic analysis using first and second polar body [J].
Verlinsky, Y ;
Rechitsky, S ;
Cieslak, J ;
Ivakhnenko, V ;
Wolf, G ;
Lifchez, A ;
Kaplan, B ;
Moise, J ;
Walle, J ;
White, M ;
Ginsberg, N ;
Strom, C ;
Kuliev, A .
BIOCHEMICAL AND MOLECULAR MEDICINE, 1997, 62 (02) :182-187