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本文引用的文献

1
CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus.CCCTC结合因子(CTCF)介导H19/胰岛素样生长因子2(Igf2)基因座处的甲基化敏感增强子阻断活性。
Nature. 2000 May 25;405(6785):486-9. doi: 10.1038/35013106.
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Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene.一种依赖CTCF的边界的甲基化控制Igf2基因的印记表达。
Nature. 2000 May 25;405(6785):482-5. doi: 10.1038/35013100.
3
Identification of an imprinted gene, Meg3/Gtl2 and its human homologue MEG3, first mapped on mouse distal chromosome 12 and human chromosome 14q.一个印记基因Meg3/Gtl2及其人类同源物MEG3的鉴定,最初定位于小鼠第12号染色体远端和人类第14号染色体q区。
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Parental origin-specific expression of Mash2 is established at the time of implantation with its imprinting mechanism highly resistant to genome-wide demethylation.Mash2的亲本来源特异性表达在着床时建立,其印记机制对全基因组去甲基化具有高度抗性。
Mech Dev. 1999 Sep;87(1-2):129-42. doi: 10.1016/s0925-4773(99)00158-6.
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The protein CTCF is required for the enhancer blocking activity of vertebrate insulators.蛋白质CTCF是脊椎动物绝缘子增强子阻断活性所必需的。
Cell. 1999 Aug 6;98(3):387-96. doi: 10.1016/s0092-8674(00)81967-4.
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The sins of the fathers and mothers: genomic imprinting in mammalian development.父母的“罪”:哺乳动物发育中的基因组印记
Cell. 1999 Jan 22;96(2):185-93. doi: 10.1016/s0092-8674(00)80559-0.
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Genetics of mouse growth.小鼠生长的遗传学
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8
Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2.H19差异甲基化区域的缺失导致H19和Igf2印记表达的丧失。
Genes Dev. 1998 Dec 1;12(23):3693-702. doi: 10.1101/gad.12.23.3693.
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Genomic imprinting is disrupted in interspecific Peromyscus hybrids.基因组印记在种间白足鼠杂交种中受到破坏。
Nat Genet. 1998 Dec;20(4):362-5. doi: 10.1038/3833.
10
Modulated expression of the epidermal growth factor-like homeotic protein dlk influences stromal-cell-pre-B-cell interactions, stromal cell adipogenesis, and pre-B-cell interleukin-7 requirements.表皮生长因子样同源蛋白dlk的表达调控影响基质细胞与前B细胞的相互作用、基质细胞脂肪生成以及前B细胞对白介素-7的需求。
Mol Cell Biol. 1998 Sep;18(9):5247-55. doi: 10.1128/MCB.18.9.5247.

Dlk1基因和Gtl2基因相互连锁且呈现反向印记。

The Dlk1 and Gtl2 genes are linked and reciprocally imprinted.

作者信息

Schmidt J V, Matteson P G, Jones B K, Guan X J, Tilghman S M

机构信息

Howard Hughes Medical Institute and Department of Molecular Biology, Princeton University, Princeton, New Jersey 08544, USA.

出版信息

Genes Dev. 2000 Aug 15;14(16):1997-2002.

PMID:10950864
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC316857/
Abstract

Genes subject to genomic imprinting exist in large chromosomal domains, probably reflecting coordinate regulation of the genes within a cluster. Such regulation has been demonstrated for the H19, Igf2, and Ins2 genes that share a bifunctional imprinting control region. We have identified the Dlk1 gene as a new imprinted gene that is paternally expressed. Furthermore, we show that Dlk1 is tightly linked to the maternally expressed Gtl2 gene. Dlk1 and Gtl2 are coexpressed and respond in a reciprocal manner to loss of DNA methylation. These genes are likely to represent a new example of coordinated imprinting of linked genes.

摘要

受到基因组印记影响的基因存在于大的染色体区域中,这可能反映了一个基因簇内各基因的协同调控。对于共享一个双功能印记控制区域的H19、Igf2和Ins2基因,这种调控已得到证实。我们已将Dlk1基因鉴定为一个新的父本表达的印记基因。此外,我们发现Dlk1与母本表达的Gtl2基因紧密连锁。Dlk1和Gtl2共同表达,并且对DNA甲基化缺失以相反的方式做出反应。这些基因可能代表了连锁基因协同印记的一个新例子。