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肉鸡代谢转换过程中肝脏有丝分裂和细胞周期转录网络的变化。

Alterations in hepatic mitotic and cell cycle transcriptional networks during the metabolic switch in broiler chicks.

作者信息

Hicks Julie A, Pike Brandon E, Liu Hsiao-Ching

机构信息

Department of Animal Science, North Carolina State University, Raleigh, NC, United States.

出版信息

Front Physiol. 2022 Oct 24;13:1020870. doi: 10.3389/fphys.2022.1020870. eCollection 2022.

Abstract

During embryonic life, chicks mainly derive energy from hepatic oxidation of yolk lipids. After hatch, chicks must rely on carbohydrate-rich feed to obtain energy. This requires an abrupt and intensive switch of metabolic processes, particularly in the liver. We recently identified a number of transcriptional and post-transcriptional regulatory networks that work concordantly to tune metabolic processes during the metabolic switch. Here, we used delayed feeding post-hatch (48 h) to impede the metabolic switch in broilers. We used RNA-seq to identify hepatic transcriptome differences between late stage embryos (E18) and two-day-old chicks (D2), which were either fed-from-hatch (FED) or not fed (DLY). Between FED and E18, 2,430 genes were differentially expressed (fold-change≥ 2; FDR -value 0.05), of these 1,237 were downregulated in FED birds and 1,193 were upregulated. Between DLY and E18, 1979 genes were differentially expressed, of these 1,043 were downregulated and 936 were upregulated in DLY birds. Between DLY and FED, 880 genes were differentially expressed, of these 543 were downregulated and 337 were upregulated in DLY birds. We found that in addition to disturbances in a number of metabolic pathways, unfed chicks had a widespread suppression of gene networks associated with cell proliferation, cell cycle progression and mitosis. Expression patterns suggest that hepatocytes of delayed-fed birds have abnormal mitosis and increased polyploidization. This suggests that post-hatch feed consumption maintains the rate and integrity of liver growth immediately, which in turn, likely helps facilitate the appropriate programming of hepatic metabolic networks.

摘要

在胚胎期,雏鸡主要从肝脏对卵黄脂质的氧化中获取能量。孵化后,雏鸡必须依靠富含碳水化合物的饲料来获取能量。这需要代谢过程发生突然且剧烈的转变,尤其是在肝脏中。我们最近发现了一些转录和转录后调控网络,它们协同作用以调节代谢转换期间的代谢过程。在此,我们采用孵化后延迟喂食(48小时)来阻碍肉鸡的代谢转换。我们使用RNA测序来鉴定晚期胚胎(E18)和两日龄雏鸡(D2)之间的肝脏转录组差异,其中D2雏鸡要么从孵化后就开始喂食(FED),要么不喂食(DLY)。在FED和E18之间,有2430个基因差异表达(倍数变化≥2;FDR值0.05),其中1237个在FED雏鸡中下调,1193个上调。在DLY和E18之间,有1979个基因差异表达,其中1043个在DLY雏鸡中下调,936个上调。在DLY和FED之间,有880个基因差异表达,其中543个在DLY雏鸡中下调,337个上调。我们发现,除了一些代谢途径受到干扰外,未喂食的雏鸡还广泛抑制了与细胞增殖、细胞周期进程和有丝分裂相关的基因网络。表达模式表明,延迟喂食雏鸡的肝细胞有异常有丝分裂且多倍体化增加。这表明孵化后进食能立即维持肝脏生长的速度和完整性,进而可能有助于促进肝脏代谢网络的适当编程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a66c/9639855/dd639594231c/fphys-13-1020870-g001.jpg

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