Gaur Pankaj, Prasad S
Biochemistry and Molecular Biology Lab, CAS in Zoology, Banaras Hindu, University, Varanasi, 221005, UP, India.
Mol Biol Rep. 2014 Oct;41(10):6855-63. doi: 10.1007/s11033-014-3571-1. Epub 2014 Jul 12.
Fragile X mental retardation protein (FMRP) has been implicated in learning, memory and cognition, therefore, information on alterations in FMRP expression during maturation and aging may provide a clue towards understanding mechanisms of age-dependent cognitive changes in the brain. In the present paper, we have studied Fmr-1 gene expression and its correlation with interaction of a tans-acting factor Sp1with Fmr-1 promoter in the cerebral cortex of female mice at post natal period during maturation and aging. Our data reveal that level of Fmr-1 transcript in the cerebral cortex is significantly up regulated at day 7 after birth compared to day 0 (the day of birth) and is gradually down regulated from day 15 onward to old age. The pattern of Fmr-1 transcript levels corresponds with the level of FMRP, however, its level is significantly up regulated in old age compared to adult mice. Our EMSA data revealed the formation of a single complex as a result of binding of Sp1with Fmr-1 promoter sequence. Its intensity gradually decreased from the day 0 (day of birth) till day 15, remained unaltered in young, significantly decreased in adult and significantly increased in old age. Our data suggests that age-dependent alteration in the Fmr-1 gene expression is associated with Sp1 interaction with Fmr-1 promoter which in turn might be related with cognitive development during brain maturation and aging.
脆性X智力低下蛋白(FMRP)与学习、记忆和认知有关,因此,关于FMRP表达在成熟和衰老过程中变化的信息可能为理解大脑中与年龄相关的认知变化机制提供线索。在本文中,我们研究了出生后成熟和衰老阶段雌性小鼠大脑皮质中Fmr-1基因的表达及其与反式作用因子Sp1与Fmr-1启动子相互作用的相关性。我们的数据显示,与出生当天(第0天)相比,出生后第7天大脑皮质中Fmr-1转录本水平显著上调,从第15天开始直至老年逐渐下调。Fmr-1转录本水平的模式与FMRP水平相对应,然而,与成年小鼠相比,其水平在老年时显著上调。我们的电泳迁移率变动分析(EMSA)数据显示,由于Sp1与Fmr-1启动子序列结合,形成了一个单一复合物。其强度从出生当天(第0天)到第15天逐渐降低,在幼年时保持不变,在成年时显著降低,在老年时显著增加。我们的数据表明,Fmr-1基因表达的年龄依赖性改变与Sp1与Fmr-1启动子的相互作用有关,这反过来可能与大脑成熟和衰老过程中的认知发展有关。