对抱窝鸡萎缩卵巢的全转录组分析揭示了与增殖和凋亡相关的调控途径。
Whole-transcriptome analysis of atrophic ovaries in broody chickens reveals regulatory pathways associated with proliferation and apoptosis.
机构信息
Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, Sichuan Agricultural University, Chengdu Campus, 611130, Sichuan Province, China.
Department of Animal and Poultry Sciences, Virginia Tech, Blacksburg, 24061, Virginia, USA.
出版信息
Sci Rep. 2018 May 8;8(1):7231. doi: 10.1038/s41598-018-25103-6.
Broodiness in laying hens results in atrophy of the ovary and consequently decreases productivity. However, the regulatory mechanisms that drive ovary development remain elusive. Thus, we collected atrophic ovaries (AO) from 380-day-old broody chickens (BC) and normal ovaries (NO) from even-aged egg-laying hens (EH) for RNA sequencing. We identified 3,480 protein-coding transcripts that were differentially expressed (DE), including 1,719 that were down-regulated and 1,761 that were up-regulated in AO. There were 959 lncRNA transcripts that were DE, including 56 that were down-regulated and 903 that were up-regulated. Among the116 miRNAs that were DE, 79 were down-regulated and 37 were up-regulated in AO. Numerous DE protein-coding transcripts and target genes for miRNAs/lncRNAs were significantly enriched in reproductive processes, cell proliferation, and apoptosis pathways. A miRNA-intersection gene-pathway network was constructed by considering target relationships and correlation of the expression levels between ovary development-related genes and miRNAs. We also constructed a competing endogenous RNA (ceRNA) network by integrating competing relationships between protein-coding genes and lncRNA transcripts, and identified several lncRNA transcripts predicted to regulate the CASP6, CYP1B1, GADD45, MMP2, and SMAS2 genes. In conclusion, we discovered protein-coding genes, miRNAs, and lncRNA transcripts that are candidate regulators of ovary development in broody chickens.
就巢母鸡会导致卵巢萎缩,从而降低生产效率。然而,驱动卵巢发育的调控机制仍然难以捉摸。因此,我们从 380 日龄的抱窝鸡(BC)中收集了萎缩卵巢(AO),并从同龄的产蛋母鸡(EH)中收集了正常卵巢(NO)进行 RNA 测序。我们鉴定出 3480 个差异表达的蛋白编码转录本,包括 1719 个下调和 1761 个上调的转录本。有 959 个 lncRNA 转录本差异表达,包括 56 个下调和 903 个上调的转录本。在 116 个差异表达的 miRNA 中,79 个下调,37 个上调。大量差异表达的蛋白编码转录本和 miRNA/lncRNA 的靶基因在生殖过程、细胞增殖和细胞凋亡途径中显著富集。通过考虑卵巢发育相关基因和 miRNA 之间的靶关系和表达水平的相关性,构建了 miRNA 互作基因-通路网络。我们还通过整合蛋白编码基因和 lncRNA 转录本之间的竞争关系,构建了一个竞争性内源 RNA (ceRNA) 网络,并预测了几个 lncRNA 转录本可能调节 CASP6、CYP1B1、GADD45、MMP2 和 SMAS2 基因。总之,我们发现了一些蛋白编码基因、miRNA 和 lncRNA 转录本,它们可能是就巢母鸡卵巢发育的候选调控因子。
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