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人类白色脂肪组织的转录组和代谢网络分析揭示的生物钟调节

Circadian regulation in human white adipose tissue revealed by transcriptome and metabolic network analysis.

机构信息

Faculty of Health and Medical Sciences, University of Surrey, Guildford, UK.

Department of Medicine, Brigham and Women's Hospital, Boston, USA.

出版信息

Sci Rep. 2019 Feb 25;9(1):2641. doi: 10.1038/s41598-019-39668-3.

DOI:10.1038/s41598-019-39668-3
PMID:30804433
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6389935/
Abstract

Studying circadian rhythms in most human tissues is hampered by difficulty in collecting serial samples. Here we reveal circadian rhythms in the transcriptome and metabolic pathways of human white adipose tissue. Subcutaneous adipose tissue was taken from seven healthy males under highly controlled 'constant routine' conditions. Five biopsies per participant were taken at six-hourly intervals for microarray analysis and in silico integrative metabolic modelling. We identified 837 transcripts exhibiting circadian expression profiles (2% of 41619 transcript targeting probes on the array), with clear separation of transcripts peaking in the morning (258 probes) and evening (579 probes). There was only partial overlap of our rhythmic transcripts with published animal adipose and human blood transcriptome data. Morning-peaking transcripts associated with regulation of gene expression, nitrogen compound metabolism, and nucleic acid biology; evening-peaking transcripts associated with organic acid metabolism, cofactor metabolism and redox activity. In silico pathway analysis further indicated circadian regulation of lipid and nucleic acid metabolism; it also predicted circadian variation in key metabolic pathways such as the citric acid cycle and branched chain amino acid degradation. In summary, in vivo circadian rhythms exist in multiple adipose metabolic pathways, including those involved in lipid metabolism, and core aspects of cellular biochemistry.

摘要

在大多数人体组织中研究昼夜节律受到收集连续样本的困难的阻碍。在这里,我们揭示了人类白色脂肪组织的转录组和代谢途径的昼夜节律。在高度控制的“恒常程序”条件下,从 7 名健康男性中取出皮下脂肪组织。每个参与者的 5 个活检每隔 6 小时进行一次微阵列分析和计算机综合代谢建模。我们确定了 837 个表现出昼夜表达谱的转录本(数组上 41619 个转录本靶向探针的 2%),早晨(258 个探针)和晚上(579 个探针)峰值的转录本明显分离。我们的节律性转录本与已发表的动物脂肪和人类血液转录组数据只有部分重叠。早晨峰值的转录本与基因表达调控、氮化合物代谢和核酸生物学有关;晚上峰值的转录本与有机酸代谢、辅酶代谢和氧化还原活性有关。计算机途径分析进一步表明昼夜节律调节脂质和核酸代谢;它还预测了柠檬酸循环和支链氨基酸降解等关键代谢途径的昼夜变化。总之,体内昼夜节律存在于多种脂肪代谢途径中,包括涉及脂质代谢和细胞生物化学核心方面的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c9c/6389935/c4c89b711005/41598_2019_39668_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c9c/6389935/12060a29fd4d/41598_2019_39668_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c9c/6389935/a2de49d52776/41598_2019_39668_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c9c/6389935/84cdbfbc0c32/41598_2019_39668_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c9c/6389935/db3b29028124/41598_2019_39668_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c9c/6389935/c4c89b711005/41598_2019_39668_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c9c/6389935/12060a29fd4d/41598_2019_39668_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c9c/6389935/a2de49d52776/41598_2019_39668_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c9c/6389935/84cdbfbc0c32/41598_2019_39668_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c9c/6389935/db3b29028124/41598_2019_39668_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c9c/6389935/c4c89b711005/41598_2019_39668_Fig5_HTML.jpg

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