A DNA Element Regulates Drug Tolerance and Withdrawal in Drosophila
Author(s) -
Xiaolei Li,
Alfredo Ghezzi,
Jascha B. Pohl,
Arun Y. Bohm,
Nigel S. Atkinson
Publication year - 2013
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0075549
Subject(s) - drug , biology , drug tolerance , gene , phenotype , drug withdrawal , drug action , pharmacogenetics , pharmacology , genetics , genotype
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.
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