Small Christopher L, Shima James E, Uzumcu Mehmet, Skinner Michael K, Griswold Michael D
Center for Reproductive Biology, School of Molecular Biosciences, Washington State University, Pullman, Washington 99164, USA.
Biol Reprod. 2005 Feb;72(2):492-501. doi: 10.1095/biolreprod.104.033696. Epub 2004 Oct 20.
The application of microarray technology to the study of mammalian organogenesis can provide greater insights into the steps necessary to elicit a functionally competent tissue. To this end, a temporal profile of gene expression was generated with the purpose of identifying changes in gene expression occurring within the developing male and female embryonic gonad. Gonad tissue was collected from mouse embryos at 11.5, 12.5, 14.5, 16.5, and 18.5 days postcoitum (dpc) and relative steady-state levels of mRNA were determined using the Affymetrix MGU74v2 microarray platform. Statistical analysis produced 3693 transcripts exhibiting differential expression during male and/or female gonad development. At 11.5 dpc, the gonad is morphologically indifferent, but at 12.5 dpc, transitions to a male or female phenotype are discernible by the appearance of testicular cords. A number of genes are expressed during this period and many share similar expression profiles in both sexes. As expected, the expression of two well-known sex determination genes, specifically Sry and Sox9, is unique to the testis. Beyond 12.5 dpc, differential gene expression becomes increasingly evident as the male and female tissue morphologically and physiologically diverges. This is evident by two unique waves of transcriptional activity occurring after 14.5 dpc in the male and female. With this study, a large number of transcripts comprising the murine transcriptome can be examined throughout male and female embryonic gonad development and allow for a more complete description of gonad differentiation and development.
将微阵列技术应用于哺乳动物器官发生的研究,可以更深入地了解形成功能健全组织所需的步骤。为此,生成了基因表达的时间图谱,目的是识别发育中的雄性和雌性胚胎性腺内发生的基因表达变化。在交配后11.5、12.5、14.5、16.5和18.5天(dpc)从小鼠胚胎中收集性腺组织,并使用Affymetrix MGU74v2微阵列平台测定mRNA的相对稳态水平。统计分析产生了3693个转录本,它们在雄性和/或雌性性腺发育过程中表现出差异表达。在11.5 dpc时,性腺在形态上尚未分化,但在12.5 dpc时,通过睾丸索的出现可以看出向雄性或雌性表型的转变。在此期间有许多基因表达,并且许多基因在两性中具有相似的表达谱。正如预期的那样,两个著名的性别决定基因,即Sry和Sox9的表达,是睾丸特有的。在12.5 dpc之后,随着雄性和雌性组织在形态和生理上的分化,差异基因表达变得越来越明显。这在雄性和雌性14.5 dpc之后出现的两个独特的转录活性波中很明显。通过这项研究,可以在雄性和雌性胚胎性腺发育的整个过程中检查构成小鼠转录组的大量转录本,并对性腺分化和发育进行更完整的描述。