Analysis of DNA (cytosine 5) methyltransferase mRNA sequence and expression in bovine preimplantation embryos, fetal and adult tissues

被引:54
作者
Golding, MC [1 ]
Westhusin, ME [1 ]
机构
[1] Texas A&M Univ, Dept Vet Physiol & Pharmacol, Coll Vet Med, College Stn, TX 77843 USA
关键词
DNA methyltransferase; DNMT; cow; bovine; preimplantation development; epigenetics; epigenome; DNA methylation; isoform; alternative transcript; tissue specific expression; fetal development; DNMT1o; DNNIT1; DNNIT2; DNNIT3a; DNMT3a4; DNMT3b; nuclear transfer; cloning; development; cDNA sequence; real time PCR; in vitro fertilization; embryo culture;
D O I
10.1016/S1567-133X(03)00121-2
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mammalian preimplantation development is a critical stage for establishment of the genomic methylation pattern and proper function of the enzymes responsible for this appear essential for normal development. To date, the vast majority of work concerning the developmental expression of the DNA cytosine 5-methyltansferases (Dnmts) has been conducted in mice. Here we report the sequence and expression of the Dnmt family during bovine preimplantation and fetal development. Bovine Dnmt mRNAs display strong sequence homology to those of human and mouse and similar to other species, exist as multiple isoforms. Two of these splice variants, which have been termed Dnmt2gamma and Dnmt3a4, represent previously unreported sequence combinations. Work presented here demonstrates early bovine embryos express mRNA coding for the somatic form of Dnmt1 and that this transcript fractionates with the ribosome. Unlike the murine model, mRNA encoding the de novo methyltransferases, Dnmt3a and 3b are present during preimplantation development and can also be found in the ribosomal subcellular fraction. Further, results of Real Time PCR analysis indicate significant differences in Dnmt mRNA expression levels exist among different tissue types as well as between fetal and adult stages. Recently, it has been postulated that the cause of abnormal methylation observed in cloned embryos may be due in part to misexpression of the Dnmt1o isoform during preimplantation development. Work presented here raises new and significant hypotheses that must be considered both regarding the cadre of DNA methyltranferases that direct epigenetic programming during normal development and regarding the implication of abnormal DNMT expression in cloned embryos. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:551 / 558
页数:8
相关论文
共 27 条
[1]   The DNA methyltransferases of mammals [J].
Bestor, TH .
HUMAN MOLECULAR GENETICS, 2000, 9 (16) :2395-2402
[2]   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
[3]   PROPERTIES AND LOCALIZATION OF DNA METHYLTRANSFERASE IN PREIMPLANTATION MOUSE EMBRYOS - IMPLICATIONS FOR GENOMIC IMPRINTING [J].
CARLSON, LL ;
PAGE, AW ;
BESTOR, TH .
GENES & DEVELOPMENT, 1992, 6 (12B) :2536-2541
[4]   A novel Dnmt3a isoform produced from an alternative promoter localizes to euchromatin and its expression correlates with active de novo methylation [J].
Chen, TP ;
Ueda, Y ;
Xie, SP ;
Li, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (41) :38746-38754
[5]   Comparison of gene transcription in cloned bovine embryos produced by different nuclear transfer techniques [J].
Daniels, R ;
Hall, VJ ;
French, AJ ;
Korfiatis, NA ;
Trounson, AO .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 2001, 60 (03) :281-288
[6]  
De Sousa P A, 1999, Cloning, V1, P63, DOI 10.1089/15204559950020102
[7]   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
[8]  
DESOUSA PA, 1993, DEVELOPMENT, V117, P1355
[9]  
Franklin BA, 2001, ACSMS HEALTH FIT J, V5, P33
[10]   Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene [J].
Howell, CY ;
Bestor, TH ;
Ding, F ;
Latham, KE ;
Mertineit, C ;
Trasler, JM ;
Chaillet, JR .
CELL, 2001, 104 (06) :829-838