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鉴定体外受精猪胚胎中的谱系标记物和抑制物。

Identification of the Lineage Markers and Inhibition of in In Vitro Fertilized Porcine Embryos.

机构信息

Department of Agricultural Biotechnology, Animal Biotechnology Major and Research Institute for Agriculture and Life Sciences, Seoul National University, Seoul 08826, Korea.

Institute of Green Bio Science and Technology, Seoul National University, Pyeongchang 25354, Korea.

出版信息

Int J Mol Sci. 2020 Oct 1;21(19):7275. doi: 10.3390/ijms21197275.

Abstract

Specification of embryonic lineages is an important question in the field of early development. Numerous studies analyzed the expression patterns of the candidate transcripts and proteins in humans and mice and clearly determined the markers of each lineage. To overcome the limitations of human and mouse embryos, the expression of the marker transcripts in each cell has been investigated using in vivo embryos in pigs. In vitro produced embryos are more accessible, can be rapidly processed with low cost. Therefore, we analyzed the characteristics of lineage markers and the effects of the DAB2 gene (trophectoderm marker) in in vitro fertilized porcine embryos. We investigated the expression levels of the marker genes during embryonic stages and distribution of the marker proteins was assayed in day 7 blastocysts. Then, the shRNA vectors were injected into the fertilized embryos and the differences in the marker transcripts were analyzed. Marker transcripts showed diverse patterns of expression, and each embryonic lineage could be identified with localization of marker proteins. In DAB2-shRNA vectors injected embryos, HNF4A and PDGFRA were upregulated. DAB2 protein level was lower in shRNA-injected embryos without significant differences. Our results will contribute to understanding of the mechanisms of embryonic lineage specification in pigs.

摘要

胚胎谱系的特化是早期发育领域的一个重要问题。许多研究分析了候选转录本和蛋白质在人类和小鼠中的表达模式,并明确确定了每个谱系的标志物。为了克服人类和小鼠胚胎的局限性,使用猪体内胚胎研究了每个细胞中标志物转录本的表达。体外产生的胚胎更容易获得,可以快速低成本地处理。因此,我们分析了谱系标志物的特征以及 DAB2 基因(滋养层标志物)在体外受精猪胚胎中的作用。我们研究了标记基因在胚胎阶段的表达水平,并在第 7 天的囊胚中检测了标记蛋白的分布。然后,将 shRNA 载体注入受精卵中,并分析标记转录本的差异。标记转录本的表达模式多样,通过定位标记蛋白可以鉴定每个胚胎谱系。在注入 DAB2-shRNA 载体的胚胎中,HNF4A 和 PDGFRA 的表达上调。shRNA 注射胚胎中的 DAB2 蛋白水平较低,但无显著差异。我们的研究结果将有助于了解猪胚胎谱系特化的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8763/7582820/2e4f1c22005e/ijms-21-07275-g001.jpg

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