Genome-wide epigenetic alterations in cloned bovine fetuses

被引:92
作者
Cezar, GG
Bartolomei, MS
Forsberg, EJ
First, NL
Bishop, MD
Eilertsen, KJ
机构
[1] Infigen Inc, De Forest, WI 53532 USA
[2] Univ Penn, Sch Med, Howard Hughes Med Inst, Dept Cell & Mol Biol, Philadelphia, PA 19104 USA
[3] Univ Wisconsin, Dept Anim Sci, Madison, WI 53706 USA
关键词
embryo; developmental biology; early development; gene regulation;
D O I
10.1095/biolreprod.102.010181
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
To gain a better understanding of global methylation differences associated with development of nuclear transfer (NT)-generated cattle, we analyzed the genome-wide methylation status of spontaneously aborted cloned fetuses, cloned fetuses, and adult clones that were derived from transgenic and nontransgenic cumulus, genital ridge, and body cell lines. Cloned fetuses were recovered from ongoing normal pregnancies and were morphologically normal. Fetuses generated by artificial insemination (AI) were used as controls. in vitro fertilization (IVF) fetuses were compared with AI controls to assess effects of in vitro culture on the 5-methylcytosine content of fetal genomes. All of the fetuses were female. Skin biopsies were obtained from cloned and AI-generated adult cows. All of the adult clones were phenotypically normal and lactating and had no history of health or reproductive disorders. Genome-wide cytosine methylation levels were monitored by reverse-phase HPLC, and results indicated reduced levels of methylated cytosine in NT-generated fetuses. In contrast, no differences were observed between adult, lactating clones and similarly aged lactating cows produced by AI. These data imply that survivability of cloned cattle may be closely related to the global DNA,methylation status. This is the first report to indicate that global methylation losses may contribute to the developmental failure of cloned bovine fetuses.
引用
收藏
页码:1009 / 1014
页数:6
相关论文
共 45 条
[1]   Altered methylation patterns in cancer cell genomes: Cause or consequence? [J].
Baylin, S ;
Bestor, TH .
CANCER CELL, 2002, 1 (04) :299-305
[2]   DNA hypermethylation in tumorigenesis - epigenetics joins genetics [J].
Baylin, SB ;
Herman, JG .
TRENDS IN GENETICS, 2000, 16 (04) :168-174
[3]   DNA methylation patterns and epigenetic memory [J].
Bird, A .
GENES & DEVELOPMENT, 2002, 16 (01) :6-21
[4]   Methylation-induced repression - Belts, braces, and chromatin [J].
Bird, AP ;
Wolffe, AP .
CELL, 1999, 99 (05) :451-454
[5]   Delayed and incomplete reprogramming of chromosome methylation patterns in bovine cloned embryos [J].
Bourc'his, D ;
Le Bourhis, D ;
Patin, D ;
Niveleau, A ;
Comizzoli, P ;
Renard, JP ;
Viegas-Péquignot, E .
CURRENT BIOLOGY, 2001, 11 (19) :1542-1546
[6]   Cloned transgenic calves produced from nonquiescent fetal fibroblasts [J].
Cibelli, JB ;
Stice, SL ;
Golueke, PJ ;
Kane, JJ ;
Jerry, J ;
Blackwell, C ;
de Leon, FAP ;
Robl, JM .
SCIENCE, 1998, 280 (5367) :1256-1258
[7]   Evaluation of gestational deficiencies in cloned sheep fetuses and placentae [J].
De Sousa, PA ;
King, T ;
Harkness, L ;
Young, LE ;
Walker, SK ;
Wilmut, I .
BIOLOGY OF REPRODUCTION, 2001, 65 (01) :23-30
[8]   Conservation of methylation reprogramming in mammalian development: Aberrant reprogramming in cloned embryos [J].
Dean, W ;
Santos, F ;
Stojkovic, M ;
Zakhartchenko, V ;
Walter, J ;
Wolf, E ;
Reik, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (24) :13734-13738
[9]  
Dean W, 1998, DEVELOPMENT, V125, P2273
[10]   Lsh, a member of the SNF2 family, is required for genome-wide methylation [J].
Dennis, K ;
Fan, T ;
Geiman, T ;
Yan, QS ;
Muegge, K .
GENES & DEVELOPMENT, 2001, 15 (22) :2940-2944