p66shc, but not p53, is involved in early arrest of in vitro-produced bovine embryos

被引:61
作者
Favetta, LA [1 ]
Robert, C [1 ]
St John, EJ [1 ]
Betts, DH [1 ]
King, WA [1 ]
机构
[1] Univ Guelph, Dept Biomed Sci, Guelph, ON N1G 2W1, Canada
基金
加拿大健康研究院;
关键词
developmental arrest; embryos; p53; p66(shc); senescence;
D O I
10.1093/molehr/gah057
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
High embryo loss occurs in the first week of bovine embryo development, with a high percentage of embryonic arrest. We hypothesized that arrested embryos enter a 'senescence-like state' and that both the cell cycle regulatory protein p53 and the stress-related protein p66(shc), which are involved in the onset of senescence in somatic cells, are responsible for this early embryonic arrest. In our in vitro production system, 13.5 +/- 0.5% of embryos arrest at the 2-4-cell stage. First cleavage occurs between 26 and 48 h post insemination (hpi), with early cleaving embryos showing only 0.6 +/- 0.3% arrest, with later cleaving embryos exhibiting up to 14.2 +/- 0.9% arrest. We compared 2-4-cell embryos collected at 28 hpi with those arrested at the 2-4-cell stage collected at day 8 post insemination. Quantification by real-time PCR and by semi-quantitative immunofluorescence showed significantly higher p66(shc) mRNA and protein levels in both arrested and late cleaving embryos versus 28 hpi embryos. By comparison, no significant changes in p53 mRNA, protein and phosphorylation levels were detected. Taken together, these results demonstrate that embryonic developmental potential is related to the time of first cleavage and that p66(shc), but not p53, is up-regulated in early arrested in vitro-produced bovine embryos.
引用
收藏
页码:383 / 392
页数:10
相关论文
共 86 条
[1]   ES cells do not activate p53-dependent stress responses and undergo p53-independent apoptosis in response to DNA damage [J].
Aladjem, MI ;
Spike, BT ;
Rodewald, LW ;
Hope, TJ ;
Klemm, M ;
Jaenisch, R ;
Wahl, GM .
CURRENT BIOLOGY, 1998, 8 (03) :145-155
[2]   Cytogenetic analysis of human preimplantation embryos following developmental arrest in vitro [J].
Almeida, PA ;
Bolton, VN .
REPRODUCTION FERTILITY AND DEVELOPMENT, 1998, 10 (06) :505-513
[3]   A functional analysis of p53 during early development of Xenopus laevis [J].
Amariglio, F ;
Tchang, F ;
Prioleau, MN ;
Soussi, T ;
Cibert, C ;
Mechali, M .
ONCOGENE, 1997, 15 (18) :2191-2199
[4]   Temporal and spatial aspects of fragmentation in early human embryos: possible effects on developmental competence and association with the differential elimination of regulatory proteins from polarized domains [J].
Antczak, M ;
Van Blerkom, J .
HUMAN REPRODUCTION, 1999, 14 (02) :429-447
[5]   Culture of preimplantation embryos: Facts and artifacts [J].
Bavister, BD .
HUMAN REPRODUCTION UPDATE, 1995, 1 (02) :91-148
[6]   Genetic regulation of embryo death and senescence [J].
Betts, DH ;
King, WA .
THERIOGENOLOGY, 2001, 55 (01) :171-191
[7]  
Betts DH, 1997, MOL REPROD DEV, V46, P114, DOI 10.1002/(SICI)1098-2795(199702)46:2&lt
[8]  
114::AID-MRD2&gt
[9]  
3.0.CO
[10]  
2-T