Clement Tracy M, Anway Matthew D, Uzumcu Mehmet, Skinner Michael K
School of Molecular Biosciences, Center for Reproductive Biology, Washington State University, Pullman, Washington 99164, USA.
Reproduction. 2007 Sep;134(3):455-72. doi: 10.1530/REP-06-0341.
Gene expression profiles during sex determination and gonadal differentiation were investigated to identify new potential regulatory factors. Embryonic day 13 (E13), E14, and E16 rat testes and ovaries were used for microarray analysis, as well as E13 testis organ cultures that undergo testis morphogenesis and develop seminiferous cords in vitro. A list of 109 genes resulted from a selective analysis for genes present in male gonadal development and with a 1.5-fold change in expression between E13 and E16. Characterization of these 109 genes potentially important for testis development revealed that cytoskeletal-associated proteins, extracellular matrix factors, and signaling factors were highly represented. Throughout the developmental period (E13-E16), sex-enriched transcripts were more prevalent in the male with 34 of the 109 genes having testis-enriched expression during sex determination. In ovaries, the total number of transcripts with a 1.5-fold change in expression between E13 and E16 was similar to the testis, but none of those genes were both ovary enriched and regulated during the developmental period. Genes conserved in sex determination were identified by comparing changing transcripts in the rat analysis herein, to transcripts altered in previously published mouse studies of gonadal sex determination. A comparison of changing mouse and rat transcripts identified 43 genes with species conservation in sex determination and testis development. Profiles of gene expression during E13-E16 rat testis and ovary development are presented and candidate genes for involvement in sex determination and testis differentiation are identified. Analysis of cellular pathways did not reveal any specific pathways involving multiple candidate genes. However, the genes and gene network identified influence numerous cellular processes with cellular differentiation, proliferation, focal contact, RNA localization, and development being predominant.
为了确定新的潜在调控因子,对性别决定和性腺分化过程中的基因表达谱进行了研究。利用胚胎第13天(E13)、E14和E16的大鼠睾丸和卵巢进行微阵列分析,以及用于体外进行睾丸形态发生和形成生精索的E13睾丸器官培养。通过对雄性性腺发育中存在且在E13和E16之间表达变化1.5倍的基因进行选择性分析,得到了一份109个基因的列表。对这109个可能对睾丸发育重要的基因进行表征,发现细胞骨架相关蛋白、细胞外基质因子和信号因子高度富集。在整个发育时期(E13 - E16),性别富集转录本在雄性中更为普遍,109个基因中有34个在性别决定期间具有睾丸富集表达。在卵巢中,E13和E16之间表达变化1.5倍的转录本总数与睾丸相似,但这些基因在发育期间均未同时在卵巢中富集和受到调控。通过将本文大鼠分析中变化的转录本与先前发表的小鼠性腺性别决定研究中改变的转录本进行比较,确定了性别决定中保守的基因。对小鼠和大鼠变化转录本的比较确定了43个在性别决定和睾丸发育中具有物种保守性的基因。展示了E13 - E16大鼠睾丸和卵巢发育过程中的基因表达谱,并确定了参与性别决定和睾丸分化的候选基因。细胞途径分析未揭示任何涉及多个候选基因的特定途径。然而,所确定的基因和基因网络影响众多细胞过程,其中细胞分化、增殖、粘着斑、RNA定位和发育最为突出。