Improvements in cloning efficiencies may be possible by increasing uniformity in recipient oocytes and donor cells

被引:70
作者
Miyoshi, K
Rzucidlo, SJ
Pratt, SL
Stice, SL
机构
[1] Univ Georgia, Dept Anim & Dairy Sci, Athens, GA 30602 USA
[2] ProLinia Inc, Athens, GA 30602 USA
关键词
developmental biology; early development; ovum; pregnancy; reproductive technology;
D O I
10.1095/biolreprod.102.010876
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The low efficiency of somatic cell cloning is the major obstacle to widespread use of this technology. Incomplete nuclear reprogramming following the transfer of donor nuclei into recipient oocytes has been implicated as a primary reason for the low efficiency of the cloning procedure. The mechanisms and factors that affect the progression of the nuclear reprogramming process have not been completely elucidated, but the identification of these factors and their subsequent manipulation would increase cloning efficiency. At present, many groups are studying donor nucleus reprogramming. Here, we present an approach in which the efficiency of producing viable offspring is improved by selecting recipient oocytes and donor cells that will produce cloned embryos with functionally reprogrammed nuclei. This approach will produce information useful in future studies aimed at further deciphering the nuclear reprogramming process.
引用
收藏
页码:1079 / 1086
页数:8
相关论文
共 112 条
[1]  
AI Y, 2002, NAT BIOTECHNOL, V20, P251
[2]   The cyclin-dependent kinase inhibitors olomoucine and roscovitine arrest human fibroblasts in G1 phase by specific inhibition of CDK2 kinase activity [J].
Alessi, F ;
Quarta, S ;
Savio, M ;
Riva, F ;
Rossi, L ;
Stivala, LA ;
Scovassi, AI ;
Meijer, L ;
Prosperi, E .
EXPERIMENTAL CELL RESEARCH, 1998, 245 (01) :8-18
[3]   Production of transgenic bovine embryos by transfer of transfected granulosa cells into enucleated oocytes [J].
Arat, S ;
Rzucidlo, SJ ;
Gibbons, J ;
Miyoshi, K ;
Stice, SL .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 2001, 60 (01) :20-26
[4]   Production of goats by somatic cell nuclear transfer [J].
Baguisi, A ;
Behboodi, E ;
Melican, DT ;
Pollock, JS ;
Destrempes, MM ;
Cammuso, C ;
Williams, JL ;
Nims, SD ;
Porter, CA ;
Midura, P ;
Palacios, MJ ;
Ayres, SL ;
Denniston, RS ;
Hayes, ML ;
Ziomek, CA ;
Meade, HM ;
Godke, RA ;
Gavin, WG ;
Overström, EW ;
Echelard, Y .
NATURE BIOTECHNOLOGY, 1999, 17 (05) :456-461
[5]   INFLUENCE OF RECIPIENT OOCYTE CELL-CYCLE STAGE ON DNA-SYNTHESIS, NUCLEAR-ENVELOPE BREAKDOWN, CHROMOSOME CONSTITUTION, AND DEVELOPMENT IN NUCLEAR TRANSPLANT BOVINE EMBRYOS [J].
BARNES, FL ;
COLLAS, P ;
POWELL, R ;
KING, WA ;
WESTHUSIN, M ;
SHEPHERD, D .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 1993, 36 (01) :33-41
[6]   Production of cloned pigs from in vitro systems [J].
Betthauser, J ;
Forsberg, E ;
Augenstein, M ;
Childs, L ;
Eilertsen, K ;
Enos, J ;
Forsythe, T ;
Golueke, P ;
Jurgella, G ;
Koppang, R ;
Lesmeister, T ;
Mallon, K ;
Mell, G ;
Misica, P ;
Pace, M ;
Pfister-Genskow, M ;
Strelchenko, N ;
Voelker, G ;
Watt, S ;
Thompson, S ;
Bishop, M .
NATURE BIOTECHNOLOGY, 2000, 18 (10) :1055-1059
[7]   Cloned pigs generated from cultured skin fibroblasts derived from a H-transferase transgenic boar [J].
Bondioli, K ;
Ramsoondar, J ;
Williams, B ;
Costa, C ;
Fodor, W .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 2001, 60 (02) :189-195
[8]   Production of cloned pigs from cultured fetal fibroblast cells [J].
Boquest, AC ;
Grupen, CG ;
Harrison, SJ ;
McIlfatrick, SM ;
Ashman, RJ ;
d'Apice, AJF ;
Nottle, MB .
BIOLOGY OF REPRODUCTION, 2002, 66 (05) :1283-1287
[9]  
Bordignon V, 1998, MOL REPROD DEV, V49, P29, DOI 10.1002/(SICI)1098-2795(199801)49:1&lt
[10]  
29::AID-MRD4&gt