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Microarray Analysis of Differentially Expressed Genes in the Brains of Tubby Mice

机译:绒毛小鼠脑中差异表达基因的微阵列分析

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摘要

The tubby mouse is characterized by progressive retinal and cochlear degeneration and late-onset obesity. These phenotypes are caused by a loss-of-function mutation in the tub gene and are shared with several human syndromes, suggesting the importance of tubby protein in central nervous system (CNS) functioning. Although evidence suggests that tubby may act as a transcription factor mediating G-protein coupled receptor (GPCR) signaling, any downstream gene regulated by tubby has yet to be identified. To explore potential target genes of tubby with region-specific transcription patterns in the brain, we performed a microarray analysis using the cerebral cortex and hypothalamus of tubby mice. We also validated the changes of gene expression level observed with the microarray analysis using real-time RT-PCR. We found that expression of erythroid differentiation factor 1 (Erdr1) and caspase 1 (Casp1) increased, while p21-activated kinase 1 (Pak1) and cholecystokinin 2 receptor (Cck2r) expression decreased in the cerebral cortex of tubby mice. In the hypothalamic region, Casp 1 was up-regulated and µ-crystallin (CRYM) was down-regulated. Based on the reported functions of the differentially expressed genes, these individual or grouped genes may account for the phenotype of tubby mice. We discussed how altered expression of genes in tubby mice might be understood as the underlying mechanism behind tubby phenotypes.
机译:矮胖小鼠的特征是进行性视网膜和耳蜗变性以及迟发性肥胖。这些表型是由tub基因的功能丧失突变引起的,并与几种人类综合征共有,这表明tubby蛋白在中枢神经系统(CNS)功能中的重要性。尽管有证据表明,tubby可能充当介导G蛋白偶联受体(GPCR)信号的转录因子,但尚未确定由tubby调控的任何下游基因。为了探索在大脑中具有特定区域转录模式的海豚的潜在靶基因,我们使用海豚小鼠的大脑皮层和下丘脑进行了微阵列分析。我们还验证了使用实时RT-PCR通过微阵列分析观察到的基因表达水平的变化。我们发现,红细胞分化因子1(Erdr1)和胱天蛋白酶1(Casp1)的表达增加,而p21激活的激酶1(Pak1)和胆囊收缩素2受体(Cck2r)的表达在tubby小鼠的大脑皮层中减少。在下丘脑区域,Casp 1上调,而μ-crystallin(CRYM)下调。基于差异表达基因的报道功能,这些单个或分组的基因可能解释了矮胖小鼠的表型。我们讨论了如何在tubby小鼠中改变基因的表达,将其理解为tubby表型背后的潜在机制。

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