Chalmel Frédéric, Rolland Antoine D, Niederhauser-Wiederkehr Christa, Chung Sanny S W, Demougin Philippe, Gattiker Alexandre, Moore James, Patard Jean-Jacques, Wolgemuth Debra J, Jégou Bernard, Primig Michael
Biozentrum and Swiss Institute of Bioinformatics, Klingelbergstrasse 50-70, CH-4056 Basel, Switzerland.
Proc Natl Acad Sci U S A. 2007 May 15;104(20):8346-51. doi: 10.1073/pnas.0701883104. Epub 2007 May 2.
We report a cross-species expression profiling analysis of the human, mouse, and rat male meiotic transcriptional program, using enriched germ cell populations, whole gonads, and high-density oligonucleotide microarrays (GeneChips). Among 35% of the protein-coding genes present in rodent and human genomes that were found to be differentially expressed between germ cells and somatic controls, a key group of 357 conserved core loci was identified that displays highly similar meiotic and postmeiotic patterns of transcriptional induction across all three species. Genes known to be important for sexual reproduction are significantly enriched among differentially expressed core loci and a smaller group of conserved genes not detected in 17 nontesticular somatic tissues, correlating transcriptional activation and essential function in the male germ line. Some genes implicated in the etiology of cancer are found to be strongly transcribed in testis, suggesting that these genes may play unexpected roles in sexual reproduction. Expression profiling data further identified numerous conserved genes of biological and clinical interest previously unassociated with the mammalian male germ line.
我们报告了一项针对人类、小鼠和大鼠雄性减数分裂转录程序的跨物种表达谱分析,该分析使用了富集的生殖细胞群体、整个性腺以及高密度寡核苷酸微阵列(基因芯片)。在啮齿动物和人类基因组中存在的35%的蛋白质编码基因中,发现生殖细胞与体细胞对照之间存在差异表达,由此鉴定出一组关键的357个保守核心基因座,它们在所有三个物种中均呈现出高度相似的减数分裂和减数分裂后转录诱导模式。已知对有性生殖重要的基因在差异表达的核心基因座中显著富集,并且在17种非睾丸体细胞组织中未检测到一小部分保守基因,这与雄性生殖系中的转录激活和基本功能相关。发现一些与癌症病因有关的基因在睾丸中强烈转录,这表明这些基因可能在有性生殖中发挥意想不到的作用。表达谱数据进一步鉴定出许多先前与哺乳动物雄性生殖系无关的具有生物学和临床意义的保守基因。