McClintick Jeanette N, Crabb David W, Tian Huijun, Pinaire Jane, Smith Jennifer R, Jerome Ronald E, Edenberg Howard J
Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202-5251, USA.
J Nutr Biochem. 2006 May;17(5):345-55. doi: 10.1016/j.jnutbio.2005.08.006. Epub 2005 Sep 19.
Vitamin A (retinol) metabolites are ligands for transcription factors that regulate many genes. The liver is the main storage depot for retinol and plays a role in vitamin A homeostasis. To better understand the effects of vitamin A deficiency on liver gene expression, we produced retinol deficiency in male rats by feeding a diet low in retinol for 53 days after weaning and examined the effects on gene expression in liver using Affymetrix oligonucleotide microarrays. We detected expression of 41% of the 8799 probe sets represented on the RGU-34A GeneChips. Vitamin A deficiency resulted in major changes in liver gene expression: 805 genes (22% of all genes detected) differed at P<or=.05 (false discovery rate <0.143). Genes involved in fatty acid metabolism, peroxisomal function, glycolysis, glutamate metabolism and the urea cycle were altered. The expression of many sexually dimorphic genes was altered toward a feminized or senescent pattern of gene expression in the liver. Retinol deficiency also produces a shift toward increased protein and fat catabolism and decreased fatty acid synthesis.
维生素A(视黄醇)代谢产物是调控许多基因的转录因子的配体。肝脏是视黄醇的主要储存库,在维生素A稳态中发挥作用。为了更好地理解维生素A缺乏对肝脏基因表达的影响,我们在雄性大鼠断奶后用低视黄醇饮食喂养53天,使其产生视黄醇缺乏,并使用Affymetrix寡核苷酸微阵列检测对肝脏基因表达的影响。我们检测到RGU - 34A基因芯片上8799个探针组中41%的表达。维生素A缺乏导致肝脏基因表达发生重大变化:805个基因(占所有检测基因的22%)在P≤0.05(错误发现率<0.143)时有差异。参与脂肪酸代谢、过氧化物酶体功能、糖酵解、谷氨酸代谢和尿素循环的基因发生了改变。许多性二态性基因的表达朝着肝脏中女性化或衰老的基因表达模式改变。视黄醇缺乏还导致蛋白质和脂肪分解代谢增加以及脂肪酸合成减少的转变。