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Divergent gene expression through PI3K/akt signalling pathway cause different models of hypertrophy growth in chicken

机译:通过PI3K / AKT信号通路的发散基因表达导致鸡肉中的肥大生长模型

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摘要

RNA-Seq technology was used to investigate differences in the gene expression of pectoralis muscle tissue between two chicken breeds [Ross as commercial (rapidly growing) and Isfahani as Iranian local breed (slow-growing)]. Total RNA was isolated from breast muscle samples at end of 4 weeks of age and sequenced by an Illumina Hiseq 2000 sequencer. Hierarchical Indexing for Spliced Alignment of Transcripts (HISAT2) was applied to align clean reads to chicken reference genome. Then, Cufflinks package was used to assemble transcripts and identify significantly differentially expressed genes (DEGs). Between two groups, the 606 significantly DEGs were identified (p-adjusted ≤.05). The confirmation of RNA-seq data was performed by Quantitative real-time PCR (qRT-PCR), consistent expression results were found for 10 selected genes. This study identified DEGs that regulate peroxisome proliferator-activated receptors (PPAR) signalling and Phosphatidylinositol-3 kinase Akt (PI3K/Akt) pathways in the Commercial breed, which might contribute to its higher metabolism of energy and growth characteristics compared to the Native breed. Our results suggested that the different expression patterns of some interesting genes including the PIK3IP1, SGK1, FOXO3, FBXO32, FBXO30, CUL3 and ASB1 in Native chicken might represent a cause for the poor growth performance for this breed than the Commercial breed.Research highlights Expression patterns of PIK3IP1, FoxO3 and FBXO32 and some other genes might represent a cause for the poor growth performance in Native chickens. DEGs that regulate PPAR signalling and PI3K/Akt pathways, which might contribute to the higher metabolism of energy and growth characteristics in Commercial chickens. Some important candidate genes related to skeletal muscle growth is obtained.
机译:RNA-SEQ技术用于探讨两只鸡肉品种之间胸肌组织基因表达的差异[罗斯作为商业(迅速生长)和伊斯法尼作为伊朗当地品种(缓慢生长)]。在4周龄的4周结束时从乳肌样品中分离出总RNA,并由Illumina Hiseq 2000序列仪测序。用于转录转录物(Hisat2)的拼接对准的分层索引以使清洁读入鸡参考基因组。然后,使用袖扣包装来组装转录物并鉴定显着差异表达的基因(DEG)。在两组之间,鉴定了606的显着降低(p调节≤305)。通过定量实时PCR(QRT-PCR)进行RNA-SEQ数据的确认,发现了10个选定基因的一致表达结果。本研究中鉴定调节过氧化物酶体增殖物激活受体(PPAR)信令和磷脂酰肌醇-3激酶的Akt(PI3K / Akt的)途径在商业品种,这可能有助于其更高的能量和生长特性代谢相比于天然品种DEGS。我们的研究结果表明,在天然鸡肉中包括Pik3IP1,SGK1,FOXO3,FBXO32,FBXO30,CUL3和ASB1,包括PIK3IP1,SGK1,FOXO3,FBXO32,ASB1的不同表达模式可能代表该品种的增长性能差的原因。研究突出表达式PIK3IP1,FOXO3和FBXO32和其他一些基因的模式可能代表原因对当地鸡的增长性能差。调节PPAR信号和PI3K / AKT途径的DEGS可能有助于商业鸡中的能量和生长特征的较高代谢。获得与骨骼肌生长有关的一些重要候选基因。

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