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Transcriptome profiling of sheep granulosa cells and oocytes during early follicular development obtained by Laser Capture Microdissection

机译:激光捕获显微切割术获得的早期卵泡发育过程中绵羊颗粒细胞和卵母细胞的转录组分析

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摘要

BackgroundSuccessful achievement of early folliculogenesis is crucial for female reproductive function. The process is finely regulated by cell-cell interactions and by the coordinated expression of genes in both the oocyte and in granulosa cells. Despite many studies, little is known about the cell-specific gene expression driving early folliculogenesis. The very small size of these follicles and the mixture of types of follicles within the developing ovary make the experimental study of isolated follicular components very difficult.The recently developed laser capture microdissection (LCM) technique coupled with microarray experiments is a promising way to address the molecular profile of pure cell populations. However, one main challenge was to preserve the RNA quality during the isolation of single cells or groups of cells and also to obtain sufficient amounts of RNA.Using a new LCM method, we describe here the separate expression profiles of oocytes and follicular cells during the first stages of sheep folliculogenesis.
机译:背景成功完成早期卵泡形成对于女性生殖功能至关重要。该过程通过细胞与细胞之间的相互作用以及卵母细胞和颗粒细胞中基因的协同表达而得到很好的调控。尽管进行了许多研究,但是关于驱动早期卵泡形成的细胞特异性基因表达知之甚少。这些卵泡的尺寸非常小,并且发育中的卵巢内的卵泡类型不同,这使得分离卵泡成分的实验研究变得非常困难。最近开发的激光捕获显微切割(LCM)技术与微阵列实验相结合,是解决这一问题的一种有前途的方法纯细胞群的分子概况。然而,一个主要的挑战是在分离单个细胞或一组细胞的过程中保持RNA的质量并获得足够量的RNA。使用一种新的LCM方法,我们在此描述卵母细胞和卵泡细胞在分离过程中的独立表达谱。绵羊卵泡形成的第一阶段。

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