Levi Liraz, Pekarski Irena, Gutman Ellen, Fortina Paolo, Hyslop Terry, Biran Jakob, Levavi-Sivan Berta, Lubzens Esther
Department Marine Biology and Biotechnology, Israel Oceanographic and Limnological Research, Haifa, Israel.
BMC Genomics. 2009 Mar 31;10:141. doi: 10.1186/1471-2164-10-141.
In oviparous vertebrates, including fish, vitellogenesis consists of highly regulated pathways involving 17beta-estradiol (E2). Previous studies focused on a relatively small number of hepatic expressed genes during vitellogenesis. This study aims to identify hepatic genes involved in vitellogenesis and regulated by E2, by using zebrafish microarray gene expression profiling, and to provide information on functional distinctive genes expressed in the liver of a vitellogenic female, using zebrafish as a model fish.
Genes associated with vitellogenesis were revealed by the following paired t-tests (SAM) comparisons: a) two-month old vitellogenic (Vit2) females were compared with non-vitellogenic (NV) females, showing 825 differentially expressed transcripts during early stages of vitellogenesis, b) four-month old vitellogenic (Vit4) females were compared with NV females, showing 1,046 differentially expressed transcripts during vitellogenesis and c) E2-treated males were compared with control males, showing 1,828 differentially expressed transcripts regulated by E2. A Venn diagram revealed 822 common transcripts in the three groups, indicating that these transcripts were involved in vitellogenesis and putatively regulated by E2. In addition, 431 transcripts were differentially expressed in Vit2 and Vit4 females but not in E2-treated males, indicating that they were putatively not up-regulated by E2. Correspondence analysis showed high similarity in expression profiles of Vit2 with Vit4 and of NV females with control males. The E2-treated males differed from the other groups. The repertoire of genes putatively regulated by E2 in vitellogenic females included genes associated with protein synthesis and reproduction. Genes associated with the immune system processes and biological adhesion, were among the genes that were putatively not regulated by E2. E2-treated males expressed a large array of transcripts that were not associated with vitellogenesis.The study revealed several genes that were not reported before as being regulated by E2. Also, the hepatic expression of several genes was reported here for the first time.
Gene expression profiling of liver samples revealed 1,046 differentially expressed transcripts during vitellogenesis of which at least ~64% were regulated by E2. The results raise the question on the regulation pattern and temporal pleiotropic expression of hepatic genes in vitellogenic females.
在包括鱼类在内的卵生脊椎动物中,卵黄生成由涉及17β-雌二醇(E2)的高度调控途径组成。先前的研究聚焦于卵黄生成过程中相对少量的肝脏表达基因。本研究旨在通过斑马鱼微阵列基因表达谱分析来鉴定参与卵黄生成并受E2调控的肝脏基因,并以斑马鱼作为模式鱼类,提供有关卵黄生成期雌性肝脏中表达的功能独特基因的信息。
通过以下配对t检验(SAM)比较揭示了与卵黄生成相关的基因:a)将两个月大的卵黄生成期(Vit2)雌性与非卵黄生成期(NV)雌性进行比较,发现在卵黄生成早期有825个差异表达的转录本;b)将四个月大的卵黄生成期(Vit4)雌性与NV雌性进行比较,发现在卵黄生成过程中有1046个差异表达的转录本;c)将E2处理的雄性与对照雄性进行比较,发现有1828个受E2调控的差异表达转录本。维恩图显示三组中有822个共同的转录本,表明这些转录本参与卵黄生成并可能受E2调控。此外,有431个转录本在Vit2和Vit4雌性中差异表达,但在E2处理的雄性中未差异表达,表明它们可能不受E2上调。对应分析显示Vit2与Vit4以及NV雌性与对照雄性的表达谱具有高度相似性。E2处理的雄性与其他组不同。卵黄生成期雌性中可能受E2调控的基因库包括与蛋白质合成和生殖相关的基因。与免疫系统过程和生物黏附相关的基因,属于可能不受E2调控的基因。E2处理的雄性表达了大量与卵黄生成无关的转录本。该研究揭示了几个以前未报道受E2调控的基因。此外,这里首次报道了几个基因的肝脏表达情况。
肝脏样本的基因表达谱分析发现在卵黄生成过程中有1046个差异表达的转录本,其中至少约64%受E2调控。这些结果引发了关于卵黄生成期雌性肝脏基因调控模式和时间多效性表达的问题。