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Endometrial gene expression in high- and low-fertility heifers in the late luteal phase of the estrous cycle and a comparison with midluteal gene expression

机译:黄体期黄体期高低生育期小母牛子宫内膜基因表达及其与中黄体基因表达的比较

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Embryonic mortality is a major constraint to improving reproductive efficiency and profitability in livestock enterprises. We previously reported differential expression of genes with identified roles in cellular growth and proliferation, lipid metabolism, endometrial remodeling, inflammation, angiogenesis, and metabolic exchange in endometrial tissue on day 7 of the estrous cycle (D7), between heifers ranked as either high (HF) or low (LF) for fertility. The aim of the current study was to further elucidate the underlying molecular mechanisms contributing to early embryo loss by examining differential endometrial gene expression in HF or LF heifers at a later stage of the estrous cycle; day 14 (D14). A second objective was to compare these expression profiles with those from midluteal HF and LF endometrium. Using the same animal model as employed in the previous study, we slaughtered HF and LF animals on D14, harvested endometrial tissue, and carried out global gene expression analysis using the Affymetrix Bovine GeneChip. Microarray analysis detected 430 differentially expressed genes (DEG) between HF and LF animals. Ingenuity Pathway Analysis revealed enrichment for a host of biological pathways including lipid metabolism, molecular transport, immune response, cell morphology and development, and cell growth and proliferation. Important DEG included ALB, BMPR2, CCL28, COL4A3/4, FADS1, ITGA6, LDLR, PLCB3, PPARG, PTGS2, and SLC27A4. Furthermore, DEG expressed on both D7 and D14 included: PCCB, SLC25A24, DAP, and COL4A4. This study highlights some of the pathways and mechanisms underpinning late luteal bovine endometrial physiology and endometrial-related conception rate variance.
机译:胚胎死亡率是提高畜牧企业繁殖效率和盈利能力的主要制约因素。我们先前曾报道在发情周期(D7)的第7天,在排名为高( HF)或低(LF)的生育力。本研究的目的是通过在发情周期的后期检查HF或LF小母牛的子宫内膜异位基因表达,进一步阐明促成早期胚胎丢失的潜在分子机制。第14天(D14)。第二个目的是将这些表达谱与黄体中层HF和LF子宫内膜的表达谱进行比较。使用与先前研究相同的动物模型,我们在D14处屠宰了HF和LF动物,收获了子宫内膜组织,并使用Affymetrix牛GeneChip进行了全局基因表达分析。微阵列分析检测到HF和LF动物之间的430个差异表达基因(DEG)。创造力途径分析揭示了丰富的生物途径,包括脂质代谢,分子转运,免疫反应,细胞形态和发育以及细胞生长和增殖。重要的DEG包括ALB,BMPR2,CCL28,COL4A3 / 4,FADS1,ITGA6,LDLR,PLCB3,PPARG,PTGS2和SLC27A4。此外,在D7和D14上表达的DEG包括:PCCB,SLC25A24,DAP和COL4A4。这项研究突出了支持黄体黄体晚期子宫内膜生理和与子宫内膜相关的受胎率变化的一些途径和机制。

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