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相似文献

1
The mouse Murr1 gene is imprinted in the adult brain, presumably due to transcriptional interference by the antisense-oriented U2af1-rs1 gene.小鼠Murr1基因在成体大脑中呈现印记状态,推测这是由于反义方向的U2af1-rs1基因的转录干扰所致。
Mol Cell Biol. 2004 Jan;24(1):270-9. doi: 10.1128/MCB.24.1.270-279.2004.
2
Comparative analyses of genomic imprinting and CpG island-methylation in mouse Murr1 and human MURR1 loci revealed a putative imprinting control region in mice.对小鼠Murr1和人类MURR1基因座中的基因组印记和CpG岛甲基化进行的比较分析揭示了小鼠中一个假定的印记控制区域。
Gene. 2006 Jan 17;366(1):77-86. doi: 10.1016/j.gene.2005.08.020. Epub 2005 Nov 21.
3
Mouse U2af1-rs1 is a neomorphic imprinted gene.小鼠U2af1-rs1是一个新形态印记基因。
Mol Cell Biol. 1997 Feb;17(2):789-98. doi: 10.1128/MCB.17.2.789.
4
DNA methylation is linked to deacetylation of histone H3, but not H4, on the imprinted genes Snrpn and U2af1-rs1.DNA甲基化与印记基因Snrpn和U2af1-rs1上组蛋白H3而非H4的去乙酰化有关。
Mol Cell Biol. 2001 Aug;21(16):5426-36. doi: 10.1128/MCB.21.16.5426-5436.2001.
5
Identification of a novel isoform of Murr1 transcript, U2mu, which is transcribed from the portions of two closely located but oppositely oriented genes.鉴定出一种新型的Murr1转录本异构体U2mu,它是从两个紧密相邻但方向相反的基因部分转录而来的。
Genes Genet Syst. 2002 Oct;77(5):377-81. doi: 10.1266/ggs.77.377.
6
Aberrant methylation of an imprinted gene U2af1-rs1(SP2) caused by its own transgene.由其自身转基因导致的印记基因U2af1-rs1(SP2)的异常甲基化。
J Biol Chem. 1997 Apr 4;272(14):9120-2. doi: 10.1074/jbc.272.14.9120.
7
Inactive allele-specific methylation and chromatin structure of the imprinted gene U2af1-rs1 on mouse chromosome 11.小鼠11号染色体上印记基因U2af1-rs1的无活性等位基因特异性甲基化和染色质结构
Genomics. 1996 Jul 1;35(1):248-52. doi: 10.1006/geno.1996.0348.
8
Parental chromosome-specific chromatin conformation in the imprinted U2af1-rs1 gene in the mouse.小鼠中印记U2af1-rs1基因的亲本染色体特异性染色质构象。
J Biol Chem. 1997 Aug 15;272(33):20893-900. doi: 10.1074/jbc.272.33.20893.
9
Association of a redefined proximal mouse chromosome 11 imprinting region and U2afbp-rs/U2af1-rs1 expression.重新定义的近端小鼠11号染色体印记区域与U2afbp-rs/U2af1-rs1表达的关联
Cytogenet Cell Genet. 1998;80(1-4):41-7. doi: 10.1159/000014955.
10
Inhibition of histone deacetylases alters allelic chromatin conformation at the imprinted U2af1-rs1 locus in mouse embryonic stem cells.组蛋白去乙酰化酶的抑制作用改变了小鼠胚胎干细胞中印迹U2af1-rs1基因座的等位基因染色质构象。
J Biol Chem. 2002 Apr 5;277(14):11728-34. doi: 10.1074/jbc.M105775200. Epub 2002 Jan 30.

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1
Methylation-induced suppression of BEX1 activates AKT/ERK/STAT3 signaling pathways regulating cell cycle and apoptosis in glioma.甲基化诱导的BEX1抑制激活调节胶质瘤细胞周期和凋亡的AKT/ERK/STAT3信号通路。
Sci Rep. 2025 Aug 13;15(1):29716. doi: 10.1038/s41598-025-14123-8.
2
Genomic imprinting in mouse blastocysts is predominantly associated with H3K27me3.小鼠囊胚中的基因组印记主要与 H3K27me3 相关。
Nat Commun. 2021 Jun 21;12(1):3804. doi: 10.1038/s41467-021-23510-4.
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Sex-Dimorphic Behavioral Alterations and Altered Neurogenesis in U12 Intron Splicing-Defective Mutant Mice.U12 内含子剪接缺陷突变小鼠的性别二态性行为改变和神经发生改变。
Int J Mol Sci. 2019 Jul 19;20(14):3543. doi: 10.3390/ijms20143543.
4
Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR.在印迹 Zrsr1-DMR 处,生长卵母细胞特异性转录依赖性从头 DNA 甲基化。
Epigenetics Chromatin. 2018 Jun 6;11(1):28. doi: 10.1186/s13072-018-0200-6.
5
Genomic imprinting does not reduce the dosage of UBE3A in neurons.基因组印记不会降低神经元中UBE3A的剂量。
Epigenetics Chromatin. 2017 May 15;10:27. doi: 10.1186/s13072-017-0134-4. eCollection 2017.
6
Analysis of Genome-Wide Monoallelic Expression Patterns in Three Major Cell Types of Mouse Visual Cortex Using Laser Capture Microdissection.使用激光捕获显微切割技术分析小鼠视觉皮层三种主要细胞类型中的全基因组单等位基因表达模式。
PLoS One. 2016 Sep 23;11(9):e0163663. doi: 10.1371/journal.pone.0163663. eCollection 2016.
7
New Perspectives on Genomic Imprinting, an Essential and Multifaceted Mode of Epigenetic Control in the Developing and Adult Brain.基因组印记的新视角,一种在发育中和成体大脑中至关重要且多方面的表观遗传调控模式。
Annu Rev Neurosci. 2016 Jul 8;39:347-84. doi: 10.1146/annurev-neuro-061010-113708. Epub 2016 Apr 25.
8
Germline and somatic imprinting in the nonhuman primate highlights species differences in oocyte methylation.非人灵长类动物中的种系印记和体细胞印记突出了卵母细胞甲基化的物种差异。
Genome Res. 2015 May;25(5):611-23. doi: 10.1101/gr.183301.114. Epub 2015 Apr 10.
9
Transcriptomic changes in brain development.大脑发育过程中的转录组变化。
Int Rev Neurobiol. 2014;116:233-50. doi: 10.1016/B978-0-12-801105-8.00009-6.
10
High-throughput sequencing reveals the disruption of methylation of imprinted gene in induced pluripotent stem cells.高通量测序揭示了诱导多能干细胞中印迹基因甲基化的破坏。
Cell Res. 2014 Mar;24(3):293-306. doi: 10.1038/cr.2013.173. Epub 2013 Dec 31.

本文引用的文献

1
Identification of novel imprinted genes in a genome-wide screen for maternal methylation.在全基因组范围内筛选母源甲基化过程中鉴定新的印记基因。
Genome Res. 2003 Apr;13(4):558-69. doi: 10.1101/gr.781503.
2
Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals.基因表达的表观遗传调控:基因组如何整合内在和环境信号。
Nat Genet. 2003 Mar;33 Suppl:245-54. doi: 10.1038/ng1089.
3
Gene silencing in phenomena related to DNA repair.
Oncogene. 2002 Dec 16;21(58):9033-42. doi: 10.1038/sj.onc.1206095.
4
Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region.小鼠7F4/F5染色体上Kip2/Lit1亚结构域中印迹簇的结构域调控:大规模DNA甲基化分析表明DMR-Lit1是一个假定的印迹控制区域。
Genome Res. 2002 Dec;12(12):1860-70. doi: 10.1101/gr.110702.
5
Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1.KvDMR1靶向缺失小鼠的印记区域丢失和生长缺陷
Nat Genet. 2002 Nov;32(3):426-31. doi: 10.1038/ng988. Epub 2002 Sep 9.
6
Antisense RNA in imprinting: spreading silence through Air.印记中的反义RNA:通过Air传播沉默。
Trends Genet. 2002 Sep;18(9):434-7. doi: 10.1016/s0168-9525(02)02749-x.
7
Integrating mRNA processing with transcription.将信使核糖核酸加工与转录整合
Cell. 2002 Feb 22;108(4):501-12. doi: 10.1016/s0092-8674(02)00617-7.
8
The non-coding Air RNA is required for silencing autosomal imprinted genes.非编码Air RNA是沉默常染色体印记基因所必需的。
Nature. 2002 Feb 14;415(6873):810-3. doi: 10.1038/415810a.
9
Identification of a new copper metabolism gene by positional cloning in a purebred dog population.通过在纯种犬群体中进行定位克隆鉴定一个新的铜代谢基因。
Hum Mol Genet. 2002 Jan 15;11(2):165-73. doi: 10.1093/hmg/11.2.165.
10
Parent-specific complementary patterns of histone H3 lysine 9 and H3 lysine 4 methylation at the Prader-Willi syndrome imprinting center.普拉德-威利综合征印记中心处组蛋白H3赖氨酸9和H3赖氨酸4甲基化的亲本特异性互补模式。
Am J Hum Genet. 2001 Dec;69(6):1389-94. doi: 10.1086/324469. Epub 2001 Oct 4.

小鼠Murr1基因在成体大脑中呈现印记状态,推测这是由于反义方向的U2af1-rs1基因的转录干扰所致。

The mouse Murr1 gene is imprinted in the adult brain, presumably due to transcriptional interference by the antisense-oriented U2af1-rs1 gene.

作者信息

Wang Youdong, Joh Keiichiro, Masuko Sadahiko, Yatsuki Hitomi, Soejima Hidenobu, Nabetani Akira, Beechey Colin V, Okinami Satoshi, Mukai Tsunehiro

机构信息

Department of Biomolecular Sciences, Saga Medical School, Saga 849-8501, Japan.

出版信息

Mol Cell Biol. 2004 Jan;24(1):270-9. doi: 10.1128/MCB.24.1.270-279.2004.

DOI:10.1128/MCB.24.1.270-279.2004
PMID:14673161
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC303337/
Abstract

The mouse Murr1 gene contains an imprinted gene, U2af1-rs1, in its first intron. U2af1-rs1 shows paternal allele-specific expression and is transcribed in the direction opposite to that of the Murr1 gene. In contrast to a previous report of biallelic expression of Murr1 in neonatal mice, we have found that the maternal allele is expressed predominantly in the adult brain and also preferentially in other adult tissues. This maternal-predominant expression is not observed in embryonic and neonatal brains. In situ hybridization experiments that used the adult brain indicated that Murr1 gene was maternally expressed in neuronal cells in all regions of the brain. We analyzed the developmental change in the expression levels of both Murr1 and U2af1-rs1 in the brain and liver, and we propose that the maternal-predominant expression of Murr1 results from transcriptional interference of the gene by U2af1-rs1 through the Murr1 promoter region.

摘要

小鼠Murr1基因的第一个内含子中包含一个印记基因U2af1-rs1。U2af1-rs1呈现父本等位基因特异性表达,并且其转录方向与Murr1基因相反。与之前关于新生小鼠中Murr1双等位基因表达的报道不同,我们发现母本等位基因在成年大脑中占主导表达,在其他成年组织中也优先表达。在胚胎和新生大脑中未观察到这种母本占主导的表达。使用成年大脑进行的原位杂交实验表明,Murr1基因在大脑所有区域的神经元细胞中呈母本表达。我们分析了大脑和肝脏中Murr1和U2af1-rs1表达水平的发育变化,并提出Murr1的母本占主导表达是由于U2af1-rs1通过Murr1启动子区域对该基因进行转录干扰所致。