The Waggoner Center for Alcohol and Addiction Research, Section of Neurobiology, the University of Texas at Austin, Austin, Texas, United States of America.
PLoS One. 2013 Sep 23;8(9):e75549. doi: 10.1371/journal.pone.0075549. eCollection 2013.
Drug tolerance and withdrawal are insidious responses to drugs of abuse; the first increases drug consumption while the second punishes abstention. Drosophila generate functional tolerance to benzyl alcohol sedation by increasing neural expression of the slo BK-type Ca(2+) activated K(+) channel gene. After drug clearance this change produces a withdrawal phenotype-increased seizure susceptibility. The drug-induced histone modification profile identified the 6b element (60 nt) as a drug responsive element. Genomic deletion of 6b produces the allele, slo (Δ6b), that reacts more strongly to the drug with increased induction, a massive increase in the duration of tolerance, and an increase in the withdrawal phenotype yet does not alter other slo-dependent behaviors. The 6b element is a homeostatic regulator of BK channel gene expression and is the first cis-acting DNA element shown to specifically affect the duration of a drug action.
药物耐受和戒断是对滥用药物的隐袭性反应;前者增加药物的消耗,而后者惩罚戒断。果蝇通过增加 slo BK 型 Ca(2+)激活的 K(+)通道基因的神经表达来产生对苯乙醇镇静的功能耐受。药物清除后,这种变化产生了一种戒断表型——癫痫易感性增加。药物诱导的组蛋白修饰谱确定了 6b 元件(60 个核苷酸)为药物反应元件。6b 元件的基因组缺失产生 slo (Δ6b)等位基因,该基因对药物的反应更强烈,诱导增加,耐受持续时间大大延长,戒断表型增加,但不改变其他 slo 依赖的行为。6b 元件是 BK 通道基因表达的一种体内平衡调节剂,是第一个被证明可特异性影响药物作用持续时间的顺式作用 DNA 元件。