The molecular foundations of the maternal to zygotic transition in the preimplantation embryo

被引:362
作者
Schultz, RM [1 ]
机构
[1] Univ Penn, Dept Biol, Philadelphia, PA 19104 USA
关键词
chromatin remodelling; genome activation; preimplantation development; promoter utilization; reprogramming gene expression;
D O I
10.1093/humupd/8.4.323
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
The maternal to zygotic transition is the first major transition that occurs following fertilization, and entails a dramatic reprogramming of gene expression that is essential for continued development. Although the major reprogramming of gene expression occurs during the 2-cell stage, transcription is evident in the 1-cell embryo, with the male pronucleus; supporting a significantly higher level of transcription than the female pronucleus. This difference is likely due to differences in chromatin structure as a consequence of the protamine-histone exchange. Although the 1-cell embryo is transcriptionally competent, transcription and translation appear uncoupled. This transcription, however, may mark promoters for efficient utilization in the 2-cell embryo. Genome activation in the 2-cell embryo is accompanied by a requirement for an enhancer for efficient transcription and the more efficient utilization of TATA-less promoters. These changes in promoter utilization could contribute substantially to the reprogramming of gene expression. Superimposed on genome activation is the development of a chromatin-mediated transcriptionally repressive state that is relieved by either inducing histone hyperacetylation or inhibiting the second round of DNA replication. Since genome activation appears to be a relatively opportunistic process, the development of the transcriptionally repressive state may be a major determinant in establishing the appropriate gene expression profile that is essential for continued development.
引用
收藏
页码:323 / 331
页数:9
相关论文
共 69 条
[1]  
Adenot PG, 1997, DEVELOPMENT, V124, P4615
[2]   Regulation of transcriptional activity during the first and second cell cycles in the preimplantation mouse embryo [J].
Aoki, F ;
Worrad, DM ;
Schultz, RM .
DEVELOPMENTAL BIOLOGY, 1997, 181 (02) :296-307
[3]   Induction of early transcription in one-cell mouse embryos by microinjection of the nonhistone chromosomal protein HMG-I [J].
Beaujean, N ;
Bouniol-Baly, C ;
Monod, C ;
Kissa, K ;
Jullien, D ;
Aulner, N ;
Amirand, C ;
Debey, P ;
Käs, E .
DEVELOPMENTAL BIOLOGY, 2000, 221 (02) :337-354
[4]   Nuclear translocation and carboxyl-terminal domain phosphorylation of RNA polymerase II delineate the two phases of zygotic gene activation in mammalian embryos [J].
Bellier, S ;
Chastant, S ;
Adenot, P ;
Vincent, M ;
Renard, JP ;
Bensaude, O .
EMBO JOURNAL, 1997, 16 (20) :6250-6262
[5]   Methylation-induced repression - Belts, braces, and chromatin [J].
Bird, AP ;
Wolffe, AP .
CELL, 1999, 99 (05) :451-454
[6]   CPG-RICH ISLANDS AND THE FUNCTION OF DNA METHYLATION [J].
BIRD, AP .
NATURE, 1986, 321 (6067) :209-213
[7]   TRANSCRIPTIONAL SELECTIVITY IN EARLY MOUSE EMBRYOS - A QUALITATIVE STUDY [J].
BONNEROT, C ;
VERNET, M ;
GRIMBER, G ;
BRIAND, P ;
NICOLAS, JF .
NUCLEIC ACIDS RESEARCH, 1991, 19 (25) :7251-7257
[8]   ENDOGENOUS TRANSCRIPTION OCCURS AT THE 1-CELL STAGE IN THE MOUSE EMBRYO [J].
BOUNIOL, C ;
NGUYEN, E ;
DEBEY, P .
EXPERIMENTAL CELL RESEARCH, 1995, 218 (01) :57-62
[9]  
Bustin M, 1996, PROG NUCLEIC ACID RE, V54, P35, DOI 10.1016/S0079-6603(08)60360-8
[10]  
CHRISTIANS E, 1995, DEVELOPMENT, V121, P113