Mouse ovary developmental RNA and protein markers from gene expression profiling

被引:50
作者
Herrera, L
Ottolenghi, C
Garcia-Ortiz, JE
Pellegrini, M
Manini, F
Ko, MSH
Nagaraja, R
Forabosco, A
Schlessinger, D
机构
[1] NIA, Gerontol Res Ctr, Genet Lab, Baltimore, MD 21224 USA
[2] Univ Modena, Dept Mother & Child, Policlin, I-41100 Modena, Italy
关键词
microarray; ovary; primordial follicles; development;
D O I
10.1016/j.ydbio.2004.11.029
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
To identify, genes involved in morphogenetic events during mouse ovary development, we started with microarray analyses of whole organ RNA. Transcripts for 60% of the 15,000 gene NIA panel were detected, and about 2000 were differentially expressed in nascent newborn compared to adult ovary. Highly differentially expressed transcripts included noncoding RNAs and newly detected genes involved in transcription regulation and signal transduction. The phased pattern of newborn Mouse ovary differentiation allowed LIS to (1) extend information on activity and stage specificity of cell type-specific genes; and (2) generate a list of candidate genes involved in primordial follicle formation, including podocalyxin (Podxl), PDGFR-beta, and a follistatin-domain-encoding gene Flstl. Oocyte-specific transcripts included many (e.g., Deltex2, Bicd2, and Zfp37) enriched in growing oocytes, as well as a novel family of untranslated RNA's (RLTR10) that is selectively expressed in early stage follicles. The results indicate that global expression profiling of whole organ RNA provides sensitive first-line information about ovarian histogenesis for which no in vitro cell models are currently available. Published by Elsevier Inc.
引用
收藏
页码:271 / 290
页数:20
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