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首页> 外文期刊>BMC Developmental Biology >Identification and expression analysis of genes associated with bovine blastocyst formation
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Identification and expression analysis of genes associated with bovine blastocyst formation

机译:牛胚泡形成相关基因的鉴定与表达分析

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Background Normal preimplantation embryo development encompasses a series of events including first cleavage division, activation of the embryonic genome, compaction and blastocyst formation. First lineage differentiation starts at the blastocyst stage with the formation of the trophectoderm and the inner cell mass. The main objective of this study was the detection, identification and expression analysis of genes associated with blastocyst formation in order to help us better understand this process. This information could lead to improvements of in vitro embryo production procedures. Results A subtractive cDNA library was constructed enriched for transcripts preferentially expressed at the blastocyst stage compared to the 2-cell and 8-cell stage. Sequence information was obtained for 65 randomly selected clones. The RNA expression levels of 12 candidate genes were determined throughout 3 stages of preimplantation embryo development (2-cell, 8-cell and blastocyst) and compared with the RNA expression levels of in vivo "golden standard" embryos using real-time PCR. The RNA expression profiles of 9 (75%) transcripts (KRT18, FN1, MYL6, ATP1B3, FTH1, HINT1, SLC25A5, ATP6V0B, RPL10) were in agreement with the subtractive cDNA cloning approach, whereas for the remaining 3 (25%) (ACTN1, COPE, EEF1A1) the RNA expression level was equal or even higher at the earlier developmental stages compared to the blastocyst stage. Moreover, significant differences in RNA expression levels were observed between in vitro and in vivo produced embryos. By immunofluorescent labelling, the protein expression of KRT18, FN1 and MYL6 was determined throughout bovine preimplantation embryo development and showed the same pattern as the RNA expression analyses. Conclusion By subtractive cDNA cloning, candidate genes involved in blastocyst formation were identified. For several candidate genes, important differences in gene expression were observed between in vivo and in vitro produced embryos, reflecting the influence of the in vitro culture system on the embryonic gene expression. Both RNA and protein expression analysis demonstrated that KRT18, FN1 and MYL6 are differentially expressed during preimplantation embryo development and those genes can be considered as markers for bovine blastocyst formation.
机译:背景技术正常的植入前胚胎发育包括一系列事件,包括第一次卵裂分裂,胚胎基因组激活,紧实和胚泡形成。最初的谱系分化开始于胚泡阶段,并形成滋养外胚层和内部细胞团。这项研究的主要目的是对与胚泡形成有关的基因进行检测,鉴定和表达分析,以帮助我们更好地了解这一过程。该信息可导致体外胚胎生产程序的改进。结果构建了一个消减cDNA文库,该文库富含与2细胞和8细胞阶段相比在胚泡阶段优先表达的转录本。获得了65个随机选择的克隆的序列信息。在植入前胚胎发育的三个阶段(2细胞,8细胞和胚泡)确定12个候选基因的RNA表达水平,并使用实时PCR与体内“黄金标准”胚胎的RNA表达水平进行比较。 9种(75%)转录本(KRT18,FN1,MYL6,ATP1B3,FTH1,HINT1,SLC25A5,ATP6V0B,RPL10)的RNA表达谱与减法cDNA克隆方法一致,而其余3种(25%)( ACTN1,COPE,EEF1A1)在早期发育阶段,与胚泡阶段相比,RNA表达水平相等甚至更高。此外,在体外和体内产生的胚胎之间观察到RNA表达水平的显着差异。通过免疫荧光标记,在整个牛植入前胚胎发育过程中确定了KRT18,FN1和MYL6的蛋白表达,并显示了与RNA表达分析相同的模式。结论通过减性cDNA克隆,鉴定了参与胚泡形成的候选基因。对于几个候选基因,在体内和体外产生的胚胎之间观察到基因表达的重要差异,反映了体外培养系统对胚胎基因表达的影响。 RNA和蛋白质表达分析均表明,KRT18,FN1和MYL6在植入前胚胎发育过程中差异表达,这些基因可被视为牛胚泡形成的标记。

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