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围产期大鼠小肠中CRBPII基因上组蛋白乙酰化的诱导。

Induction of histone acetylation on the CRBPII gene in perinatal rat small intestine.

作者信息

Ogura Yuko, Mochizuki Kazuki, Goda Toshinao

机构信息

Laboratory of Nutritional Physiology and COE Program in the 21st Century, University of Shizuoka School of Food and Nutritional Sciences, 52-1 Yada, Shizuoka 422-8526, Japan.

出版信息

Biochim Biophys Acta. 2007 Sep;1770(9):1289-96. doi: 10.1016/j.bbagen.2007.06.011. Epub 2007 Jul 4.

Abstract

The expression of genes associated with lipid and vitamin A metabolism is elevated when the small intestinal mucosa is maturing rapidly during the perinatal period. We have previously reported that cellular retinol-binding protein type II (CRBPII) mRNA levels rise abruptly in the rat small intestine during this period. In this study, we examined whether the acetylation of histones H3 and H4 is involved in the intestinal expression of CRBPII during the perinatal stage. The expression of cyclin D1 and cyclin B1 genes, which are markers of cell proliferation, decreased markedly during the perinatal period, whereas expression of CRBPII as well as villin, a marker of intestinal maturation, increased rapidly. Using a ChIP assay, we showed rapid induction of acetylation of the histones H3 and H4 which interacted with the promoter/enhancer region of the CRBPII gene at this time. The binding of CBP and p300, which have histone acetyltransferase activity, as well as binding of retinoid X receptor alpha (RXRalpha) increased on the CRBPII promoter/enhancer region during the perinatal period. These results suggest that CRBPII gene expression during the perinatal period is associated with abrupt acetylation of histones H3 and H4 followed by the binding of CBP/p300 and RXRalpha.

摘要

在围产期,当小肠黏膜快速成熟时,与脂质和维生素A代谢相关的基因表达会升高。我们之前报道过,在此期间大鼠小肠中细胞视黄醇结合蛋白II(CRBPII)的mRNA水平会突然升高。在本研究中,我们检测了组蛋白H3和H4的乙酰化是否参与围产期CRBPII在肠道中的表达。细胞增殖标志物细胞周期蛋白D1和细胞周期蛋白B1基因的表达在围产期显著下降,而CRBPII以及肠道成熟标志物绒毛蛋白的表达则迅速增加。通过染色质免疫沉淀(ChIP)分析,我们发现此时与CRBPII基因启动子/增强子区域相互作用的组蛋白H3和H4的乙酰化迅速诱导。在围产期,具有组蛋白乙酰转移酶活性的CBP和p300的结合以及视黄酸X受体α(RXRα)的结合在CRBPII启动子/增强子区域增加。这些结果表明,围产期CRBPII基因表达与组蛋白H3和H4的突然乙酰化相关,随后是CBP/p300和RXRα的结合。

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