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低表达核仁素的 HeLa 细胞中 mRNA 和 miRNA 表达的综合分析。

Integrated analysis of mRNA and miRNA expression in HeLa cells expressing low levels of Nucleolin.

机构信息

BioCOS Life Sciences Private Limited, AECS Layout, B-Block, Singasandra Hosur Road SAAMI Building, 851/A, 3rd Floor, Bengaluru, Karnataka, India.

Université de Lyon, Centre de Recherche en Cancérologie de Lyon, Cancer Cell Plasticity Department, UMR INSERM 1052 CNRS, 5286, Centre Léon Bérard, Lyon, France.

出版信息

Sci Rep. 2017 Aug 21;7(1):9017. doi: 10.1038/s41598-017-09353-4.

DOI:10.1038/s41598-017-09353-4
PMID:28827664
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5567140/
Abstract

Nucleolin is an essential protein that plays important roles in the regulation of cell cycle and cell proliferation. Its expression is up regulated in many cancer cells but its molecular functions are not well characterized. Nucleolin is present in the nucleus where it regulates gene expression at the transcriptional and post-transcriptional levels. Using HeLa cells depleted in nucleolin we performed an mRNA and miRNA transcriptomics analysis to identify biological pathways involving nucleolin. Bioinformatic analysis strongly points to a role of nucleolin in lipid metabolism, and in many signaling pathways. Down regulation of nucleolin is associated with lower level of cholesterol while the amount of fatty acids is increased. This could be explained by the decreased and mis-localized expression of the transcription factor SREBP1 and the down-regulation of enzymes involved in the beta-oxidation and degradation of fatty acids. Functional classification of the miRNA-mRNA target genes revealed that deregulated miRNAs target genes involved in apoptosis, proliferation and signaling pathways. Several of these deregulated miRNAs have been shown to control lipid metabolism. This integrated transcriptomic analysis uncovers new unexpected roles for nucleolin in metabolic regulation and signaling pathways paving the way to better understand the global function of nucleolin within the cell.

摘要

核仁素是一种重要的蛋白质,在细胞周期和细胞增殖的调节中发挥重要作用。它在许多癌细胞中表达上调,但分子功能尚未得到很好的表征。核仁素存在于细胞核中,在转录和转录后水平调节基因表达。使用核仁素耗竭的 HeLa 细胞,我们进行了 mRNA 和 miRNA 转录组学分析,以确定涉及核仁素的生物学途径。生物信息学分析强烈表明核仁素在脂质代谢和许多信号通路中发挥作用。核仁素的下调与胆固醇水平降低有关,而脂肪酸的量增加。这可以通过转录因子 SREBP1 的表达减少和定位错误以及参与脂肪酸β氧化和降解的酶的下调来解释。miRNA-mRNA 靶基因的功能分类表明,失调的 miRNA 靶基因参与凋亡、增殖和信号通路。其中一些失调的 miRNA 已被证明可以控制脂质代谢。这种综合的转录组学分析揭示了核仁素在代谢调节和信号通路中的新的、意想不到的作用,为更好地理解核仁素在细胞内的全局功能铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f40/5567140/efa09a93ea0f/41598_2017_9353_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f40/5567140/e10b4c86b12d/41598_2017_9353_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f40/5567140/feb6cd530902/41598_2017_9353_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f40/5567140/3030999d8626/41598_2017_9353_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f40/5567140/420ceebd9fc5/41598_2017_9353_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f40/5567140/0a41980526e6/41598_2017_9353_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f40/5567140/24579957ad58/41598_2017_9353_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f40/5567140/2c85451df97d/41598_2017_9353_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f40/5567140/9ba22f98b397/41598_2017_9353_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f40/5567140/efa09a93ea0f/41598_2017_9353_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f40/5567140/e10b4c86b12d/41598_2017_9353_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f40/5567140/feb6cd530902/41598_2017_9353_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f40/5567140/3030999d8626/41598_2017_9353_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f40/5567140/420ceebd9fc5/41598_2017_9353_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f40/5567140/0a41980526e6/41598_2017_9353_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f40/5567140/24579957ad58/41598_2017_9353_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f40/5567140/2c85451df97d/41598_2017_9353_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f40/5567140/9ba22f98b397/41598_2017_9353_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f40/5567140/efa09a93ea0f/41598_2017_9353_Fig9_HTML.jpg

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