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Hic1肿瘤抑制基因的两个修饰小鼠等位基因的产生。

Generation of two modified mouse alleles of the Hic1 tumor suppressor gene.

作者信息

Pospichalova Vendula, Tureckova Jolana, Fafilek Bohumil, Vojtechova Martina, Krausova Michaela, Lukas Jan, Sloncova Eva, Takacova Sylvia, Divoky Vladimir, Leprince Dominique, Plachy Jiri, Korinek Vladimir

机构信息

Department of Cell and Developmental Biology, Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, 142 20 Prague 4, Czech Republic.

出版信息

Genesis. 2011 Mar;49(3):142-51. doi: 10.1002/dvg.20719.

Abstract

HIC1 (hypermethylated in cancer 1) is a tumor suppressor gene located on chromosome 17p13.3, a region frequently hypermethylated or deleted in human neoplasias. In mouse, Hic1 is essential for embryonic development and exerts an antitumor role in adult animals. Since Hic1-deficient mice die perinatally, we generated a conditional Hic1 null allele by flanking the Hic1-coding region by loxP sites. When crossed to animals expressing Cre recombinase in a cell-specific manner, the Hic1 conditional mice will provide new insights into the function of Hic1 in developing and mature tissues. Additionally, we used gene targeting to replace sequence-encoding amino acids 186-893 of Hic1 by citrine fluorescent protein cDNA. We demonstrate that the distribution of Hic1-citrine fusion polypeptide corresponds to the expression pattern of wild-type Hic1. Consequently, Hic1-citrine "reporter" mice can be used to monitor the activity of the Hic1 locus using citrine fluorescence.

摘要

HIC1(癌症中高甲基化1)是一种肿瘤抑制基因,位于17号染色体p13.3区域,该区域在人类肿瘤中经常发生高甲基化或缺失。在小鼠中,Hic1对胚胎发育至关重要,并在成年动物中发挥抗肿瘤作用。由于Hic1基因缺陷的小鼠在围产期死亡,我们通过在Hic1编码区两侧侧翼loxP位点,构建了一个条件性Hic1无效等位基因。当与以细胞特异性方式表达Cre重组酶的动物杂交时,Hic1条件性小鼠将为Hic1在发育中和成熟组织中的功能提供新的见解。此外,我们使用基因打靶技术,用柠檬黄荧光蛋白cDNA替换Hic1编码氨基酸186 - 893的序列。我们证明,Hic1 - 柠檬黄融合多肽的分布与野生型Hic1的表达模式相对应。因此,Hic1 - 柠檬黄“报告基因”小鼠可用于利用柠檬黄荧光监测Hic1基因座的活性。

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