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首页> 外文期刊>The Journal of Reproduction and Development >Expression Profiling of Mouse Placental Lactogen II and Its Correlative Genes Using a cDNA Microarray Analysis in the Developmental Mouse Placenta
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Expression Profiling of Mouse Placental Lactogen II and Its Correlative Genes Using a cDNA Microarray Analysis in the Developmental Mouse Placenta

机译:使用发育期小鼠胎盘的cDNA芯片分析小鼠胎盘促乳素原II及其相关基因的表达谱。

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摘要

The placenta is a highly differentiated organ essential for embryonic growth anddevelopment. In order to search for key molecules that are associated with mouse placental lactogenII (mPL-II) gene expression, we applied mouse cDNA microarray analysis to RNAs extracted fromplacentae on days 10, 12, 14, 16 and 18 of pregnancy. Changes in gene expression were categorizedbetween days 10 and 12,12 and 14,14 and 16 and 16 and 18 of pregnancy. After microarray analysis,which had a minimum detectable fold change for differential expression of 2, we selected 10 genes,Apoa2, Apoc2, Ceacaml4, Cregl, Fmol, Igf2, Slc2al, Spink3, Spil-1 and Tpbpa, exhibiting aexpression pattern similar to the mPL-II gene. Furthermore, we performed real-time PCR analysisand in situ hybridization (ISH) to find correlative expression genes for the mPL-II gene. From theseresults, we identified a resemblance in gene expression between mPL-II and Igf2 and selected thesegenes for performance of double-fluorescence immunohistochemical staining. We colocalized theseproteins in labyrinthine trophoblast cells. These results strongly suggest that the expression of mPL-IIand Igf2 is highly related to placental development in mice. This large-scale identification of genesregulated during placentogenesis assists in further elucidation of the molecular basis ofextraembryonic development and function.
机译:胎盘是高度分化的器官,对于胚胎的生长和发育至关重要。为了搜索与小鼠胎盘催乳素II(mPL-II)基因表达相关的关键分子,我们将小鼠cDNA微阵列分析应用于妊娠第10、12、14、16和18天从胎盘中提取的RNA。基因表达的变化被分类在妊娠的第10和12、12、14、14、16、16和18天之间。经过微阵列分析后,差异表达的最小可检测倍数变化为2,我们选择了10个基因,Apoa2,Apoc2,Ceacaml4,Cregl,Fmol,Igf2,Slc2al,Spink3,Spil-1和Tpbpa,表现出类似于mPL-II基因。此外,我们进行了实时PCR分析和原位杂交(ISH),以找到mPL-II基因的相关表达基因。从这些结果,我们鉴定出了mPL-II和Igf2之间的基因表达相似,并选择了这些基因进行双荧光免疫组织化学染色。我们将这些蛋白共定位在迷宫滋养细胞中。这些结果强烈表明,mPL-II和Igf2的表达与小鼠胎盘发育高度相关。胎盘发生过程中调控基因的这种大规模鉴定有助于进一步阐明超胚发育和功能的分子基础。

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