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基因荒漠型乳腺癌易感位点 Mcs1a 调控 Nr2f1 从而改变乳腺上皮细胞的分化和增殖。

The gene desert mammary carcinoma susceptibility locus Mcs1a regulates Nr2f1 modifying mammary epithelial cell differentiation and proliferation.

机构信息

McArdle Laboratory for Cancer Research, Department of Oncology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.

出版信息

PLoS Genet. 2013 Jun;9(6):e1003549. doi: 10.1371/journal.pgen.1003549. Epub 2013 Jun 13.

Abstract

Genome-wide association studies have revealed that many low-penetrance breast cancer susceptibility loci are located in non-protein coding genomic regions; however, few have been characterized. In a comparative genetics approach to model such loci in a rat breast cancer model, we previously identified the mammary carcinoma susceptibility locus Mcs1a. We now localize Mcs1a to a critical interval (277 Kb) within a gene desert. Mcs1a reduces mammary carcinoma multiplicity by 50% and acts in a mammary cell-autonomous manner. We developed a megadeletion mouse model, which lacks 535 Kb of sequence containing the Mcs1a ortholog. Global gene expression analysis by RNA-seq revealed that in the mouse mammary gland, the orphan nuclear receptor gene Nr2f1/Coup-tf1 is regulated by Mcs1a. In resistant Mcs1a congenic rats, as compared with susceptible congenic control rats, we found Nr2f1 transcript levels to be elevated in mammary gland, epithelial cells, and carcinoma samples. Chromatin looping over ∼820 Kb of sequence from the Nr2f1 promoter to a strongly conserved element within the Mcs1a critical interval was identified. This element contains a 14 bp indel polymorphism that affects a human-rat-mouse conserved COUP-TF binding motif and is a functional Mcs1a candidate. In both the rat and mouse models, higher Nr2f1 transcript levels are associated with higher abundance of luminal mammary epithelial cells. In both the mouse mammary gland and a human breast cancer global gene expression data set, we found Nr2f1 transcript levels to be strongly anti-correlated to a gene cluster enriched in cell cycle-related genes. We queried 12 large publicly available human breast cancer gene expression studies and found that the median NR2F1 transcript level is consistently lower in 'triple-negative' (ER-PR-HER2-) breast cancers as compared with 'receptor-positive' breast cancers. Our data suggest that the non-protein coding locus Mcs1a regulates Nr2f1, which is a candidate modifier of differentiation, proliferation, and mammary cancer risk.

摘要

全基因组关联研究表明,许多低外显率乳腺癌易感性基因座位于非蛋白编码基因组区域;然而,这些基因座中只有少数得到了表征。在一项利用大鼠乳腺癌模型来模拟此类基因座的比较遗传学方法中,我们先前确定了乳腺癌易感性基因座 Mcs1a。我们现在将 Mcs1a 定位到一个基因荒漠的关键区间(277 Kb)内。Mcs1a 将乳腺癌多发性降低 50%,并以乳腺细胞自主的方式发挥作用。我们开发了一种大片段缺失的小鼠模型,该模型缺失了包含 Mcs1a 直系同源物的 535 Kb 序列。通过 RNA-seq 进行的全基因表达分析表明,在小鼠乳腺中,孤儿核受体基因 Nr2f1/Coup-tf1 受 Mcs1a 调控。与易感同基因对照大鼠相比,在抵抗性 Mcs1a 同基因大鼠中,我们发现乳腺、上皮细胞和癌样本中的 Nr2f1 转录本水平升高。从 Nr2f1 启动子到 Mcs1a 关键区间内一个强烈保守元件的约 820 Kb 序列的染色质环被鉴定出来。该元件包含一个影响人-大鼠-小鼠保守 COUP-TF 结合基序的 14 bp 插入/缺失多态性,是一个功能性 Mcs1a 候选基因。在大鼠和小鼠模型中,更高的 Nr2f1 转录本水平与更多的腔上皮乳腺细胞丰度相关。在小鼠乳腺和人类乳腺癌全基因表达数据集,我们发现 Nr2f1 转录本水平与富含细胞周期相关基因的基因簇呈强烈负相关。我们查询了 12 个大型公开可用的人类乳腺癌基因表达研究,发现与“受体阳性”乳腺癌相比,“三阴性”(ER-PR-HER2-)乳腺癌的中位 NR2F1 转录本水平始终较低。我们的数据表明,非蛋白编码基因座 Mcs1a 调节 Nr2f1,后者是分化、增殖和乳腺癌风险的候选修饰因子。

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