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1
Deciphering the Developmental Dynamics of the Mouse Liver Transcriptome.解析小鼠肝脏转录组的发育动态
PLoS One. 2015 Oct 23;10(10):e0141220. doi: 10.1371/journal.pone.0141220. eCollection 2015.
2
Moderate activation of IKK2-NF-kB in unstressed adult mouse liver induces cytoprotective genes and lipogenesis without apparent signs of inflammation or fibrosis.在未受应激的成年小鼠肝脏中,IKK2-NF-kB的适度激活可诱导细胞保护基因和脂肪生成,而无明显的炎症或纤维化迹象。
BMC Gastroenterol. 2015 Jul 30;15:94. doi: 10.1186/s12876-015-0325-z.
3
Ontogeny of hepatic energy metabolism genes in mice as revealed by RNA-sequencing.RNA测序揭示的小鼠肝脏能量代谢基因的个体发生
PLoS One. 2014 Aug 7;9(8):e104560. doi: 10.1371/journal.pone.0104560. eCollection 2014.
4
RNA-sequencing quantification of hepatic ontogeny of phase-I enzymes in mice.RNA 测序定量分析小鼠肝脏一期酶的个体发生。
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RNA-sequencing quantification of hepatic ontogeny and tissue distribution of mRNAs of phase II enzymes in mice.利用 RNA 测序对小鼠肝脏发生和 II 相酶 mRNAs 的组织分布进行定量分析。
Drug Metab Dispos. 2013 Apr;41(4):844-57. doi: 10.1124/dmd.112.050211. Epub 2013 Feb 4.
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Hepatic ontogeny and tissue distribution of mRNAs of epigenetic modifiers in mice using RNA-sequencing.使用 RNA 测序研究小鼠中表观遗传修饰因子的肝发生和组织分布的 mRNA。
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9
RNA-Seq reveals different mRNA abundance of transporters and their alternative transcript isoforms during liver development.RNA-Seq 揭示了肝发育过程中转运蛋白及其替代转录本异构体的 mRNA 丰度存在差异。
Toxicol Sci. 2012 Jun;127(2):592-608. doi: 10.1093/toxsci/kfs107. Epub 2012 Mar 27.
10
Glutaredoxin2 isoform b (Glrx2b) promotes RANKL-induced osteoclastogenesis through activation of the p38-MAPK signaling pathway.谷氧还蛋白2亚型b(Glrx2b)通过激活p38丝裂原活化蛋白激酶信号通路促进核因子κB受体活化因子配体(RANKL)诱导的破骨细胞生成。
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RNA-Seq 为研究小鼠肝脏发育过程中抗氧化成分的相对 mRNA 丰度提供了新的见解。

RNA-Seq provides new insights on the relative mRNA abundance of antioxidant components during mouse liver development.

机构信息

Department of Pharmacology, Toxicology, and Therapeutics, University of Kansas Medical Center, Kansas City, KS 66160, United States.

Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98195, United States.

出版信息

Free Radic Biol Med. 2019 Apr;134:335-342. doi: 10.1016/j.freeradbiomed.2019.01.017. Epub 2019 Jan 16.

DOI:10.1016/j.freeradbiomed.2019.01.017
PMID:30659941
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6588412/
Abstract

Mammals have developed a variety of antioxidant systems to protect them from the oxygen environment and toxic stimuli. Little is known about the mRNA abundance of antioxidant components during postnatal development of the liver. Therefore, the purpose of this study was to compare the mRNA abundance of antioxidant components during liver development. Livers from male C57BL/6J mice were collected at 12 ages from prenatal to adulthood. The transcriptome was determined by RNA-Seq with transcript abundance estimated by Cufflinks. RNA-Seq provided a complete, more accurate, and unbiased quantification of the transcriptome. Among 33 known antioxidant components examined, three ontogeny patterns of liver antioxidant components were observed: (1) Prenatal-enriched, in which the mRNAs decreased from fetal livers to adulthood, such as metallothionein and heme oxygenase-1; (2) adolescent-rich and relatively stable expression, such as peroxiredoxins; and (3) adult-rich, in which the mRNA increased with age, such as catalase and superoxide dismutase. Alternative splicing of several antioxidant genes, such as Keap1, Glrx2, Gpx3, and Txnrd1, were also detected by RNA-Seq. In summary, RNA-Seq revealed the relative abundance of hepatic antioxidant enzymes, which are important in protecting against the deleterious effects of oxidative stress.

摘要

哺乳动物已经发展出多种抗氧化系统来保护自己免受氧气环境和有毒刺激的伤害。关于肝脏在出生后的发育过程中抗氧化成分的 mRNA 丰度知之甚少。因此,本研究的目的是比较肝脏发育过程中抗氧化成分的 mRNA 丰度。从 12 个胎龄到成年的雄性 C57BL/6J 小鼠的肝脏中收集样本。使用 RNA-Seq 通过 Cufflinks 估计转录物丰度来确定转录组。RNA-Seq 提供了完整、更准确和无偏的转录组定量。在 33 种已知的抗氧化成分中,观察到三种肝脏抗氧化成分的个体发生模式:(1)产前富集型,其 mRNA 从胎儿肝脏减少到成年期,如金属硫蛋白和血红素加氧酶-1;(2)青春期丰富且相对稳定表达,如过氧化物酶;和(3)成年型,其 mRNA 随年龄增加,如过氧化氢酶和超氧化物歧化酶。几种抗氧化基因,如 Keap1、Glrx2、Gpx3 和 Txnrd1 的选择性剪接也通过 RNA-Seq 检测到。总之,RNA-Seq 揭示了肝脏抗氧化酶的相对丰度,这些酶在保护免受氧化应激的有害影响方面很重要。