Hoegh Anne Mette, Borup Rehannah, Nielsen Finn Cilius, Sørensen Steen, Hviid Thomas V F
Department of Clinical Biochemistry, Hvidovre Hospital, University of Copenhagen, Kettegaard Allé 30, 2650 Hvidovre, Denmark.
J Biomed Biotechnol. 2010;2010:787545. doi: 10.1155/2010/787545. Epub 2010 Mar 3.
Several studies point to the placenta as the primary cause of pre-eclampsia. Our objective was to identify placental genes that may contribute to the development of pre-eclampsia. RNA was purified from tissue biopsies from eleven pre-eclamptic placentas and eighteen normal controls. Messenger RNA expression from pooled samples was analysed by microarrays. Verification of the expression of selected genes was performed using real-time PCR. A surprisingly low number of genes (21 out of 15,000) were identified as differentially expressed. Among these were genes not previously associated with pre-eclampsia as bradykinin B1 receptor and a 14-3-3 protein, but also genes that have already been connected with pre-eclampsia, for example, inhibin beta A subunit and leptin. A low number of genes were repeatedly identified as differentially expressed, because they may represent the endpoint of a cascade of events effectuated throughout gestation. They were associated with transcriptional regulation and vasoregulative pathways, along with a number of hypothetical proteins and gene sequences with unknown functions.
多项研究指出胎盘是子痫前期的主要病因。我们的目标是鉴定可能导致子痫前期发生的胎盘基因。从11例子痫前期胎盘和18例正常对照的组织活检样本中纯化RNA。通过微阵列分析混合样本中的信使核糖核酸表达。使用实时聚合酶链反应对选定基因的表达进行验证。结果发现差异表达的基因数量出奇地少(15000个基因中仅有21个)。其中包括一些以前未与子痫前期相关联的基因,如缓激肽B1受体和一种14-3-3蛋白,也包括一些已经与子痫前期相关的基因,例如抑制素βA亚基和瘦素。少数基因被反复鉴定为差异表达,因为它们可能代表了整个孕期一系列事件的终点。它们与转录调控和血管调节途径相关,还与一些功能未知的假设蛋白和基因序列有关。