Transcript profiling during mouse oocyte development and the effect of gonadotropin priming and development in vitro

被引:205
作者
Pan, H
O'Brien, MJ
Wigglesworth, K
Eppig, JJ
Schultz, RM
机构
[1] Univ Penn, Dept Biol, Philadelphia, PA 19104 USA
[2] Jackson Lab, Bar Harbor, ME 04609 USA
关键词
mouse oocyte development; gene expression; microarrays; meiotic competence; developmental competence; development in vitro; gonadotropin priming;
D O I
10.1016/j.ydbio.2005.08.023
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The molecular basis for acquisition of meiotic and developmental competence, the two main outcomes of oocyte development and essential for producing an egg capable of being fertilized and supporting development to term, is largely unknown. Using microarrays, we characterized global changes in gene expression in oocytes derived from primordial, primary, secondary, small antral, and large antral follicles and used Expression Analysis Systematic Explorer (EASE) to identify biological and molecular processes that accompany these transitions and likely underpin acquisition of meiotic and developmental competence. The greatest degree of change in gene expression occurs during the primordial to primary follicle transition. Of particular interest is that specific chromosomes display significant changes in their overall transcriptional activity and that in some cases these changes are largely confined to specific regions on these chromosomes. We also examined the transcript profile of oocytes that developed in vitro, as well as following eCG priming. Remarkably, the expression profiles only differed by 4% and 2% from oocytes that developed in vivo when compared to oocytes that developed in vitro from either primordial or secondary follicles, respectively. About 1% of the genes were commonly mis-expressed, and EASE analysis revealed there is an over-representation of genes involved in transcription. Developmental competence of oocytes obtained from eCG-primed mice was substantially improved when compared to oocytes obtained from unprimed mice, and this correlated with decreased expression of genes implicated in basal transcription. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:493 / 506
页数:14
相关论文
共 62 条
[21]   CHROMOSOME-ABNORMALITIES IN HUMAN REPRODUCTIVE WASTAGE [J].
HASSOLD, TJ .
TRENDS IN GENETICS, 1986, 2 (04) :105-110
[22]   Mouse ovary developmental RNA and protein markers from gene expression profiling [J].
Herrera, L ;
Ottolenghi, C ;
Garcia-Ortiz, JE ;
Pellegrini, M ;
Manini, F ;
Ko, MSH ;
Nagaraja, R ;
Forabosco, A ;
Schlessinger, D .
DEVELOPMENTAL BIOLOGY, 2005, 279 (02) :271-290
[23]   Identifying biological themes within lists of genes with EASE [J].
Hosack, DA ;
Dennis, G ;
Sherman, BT ;
Lane, HC ;
Lempicki, RA .
GENOME BIOLOGY, 2003, 4 (10)
[24]   Sex matters in meiosis [J].
Hunt, PA ;
Hassold, TJ .
SCIENCE, 2002, 296 (5576) :2181-2183
[25]   Translating the histone code [J].
Jenuwein, T ;
Allis, CD .
SCIENCE, 2001, 293 (5532) :1074-1080
[26]   Acquisition of meiotic competence in mouse oocytes:: Absolute amounts of p34cdc2, cyclin b1, cdc25C, and wee1 in meiotically incompetent and competent oocytes [J].
Kanatsu-Shinohara, M ;
Schultz, RM ;
Kopf, GS .
BIOLOGY OF REPRODUCTION, 2000, 63 (06) :1610-1616
[27]   Alterations in the ovarian transcriptome during primordial follicle assembly and development [J].
Kezele, PR ;
Ague, JM ;
Nilsson, E ;
Skinner, MK .
BIOLOGY OF REPRODUCTION, 2005, 72 (01) :241-255
[28]   Cdc25b phosphatase is required for resumption of meiosis during oocyte maturation [J].
Lincoln, AJ ;
Wickramasinghe, D ;
Stein, P ;
Schultz, RM ;
Palko, ME ;
De Miguel, MP ;
Tessarollo, L ;
Donovan, PJ .
NATURE GENETICS, 2002, 30 (04) :446-449
[29]   Delta signaling from the germ line controls the proliferation and differentiation of the somatic follicle cells during Drosophila oogenesis [J].
López-Schier, H ;
St Johnston, D .
GENES & DEVELOPMENT, 2001, 15 (11) :1393-1405
[30]   Fertilization stimulates long-lasting oscillations of CaMKII activity in mouse eggs [J].
Markoulaki, S ;
Matson, S ;
Ducibella, T .
DEVELOPMENTAL BIOLOGY, 2004, 272 (01) :15-25