Bolduc Francois V, Valente Dan, Nguyen Antoinette T, Mitra Partha P, Tully Tim
Watson School of Biological Sciences, Cold Spring Harbor, NY, USA.
Fly (Austin). 2010 Jul-Sep;4(3):216-25. doi: 10.4161/fly.4.3.12280. Epub 2010 Jul 1.
We developed a novel assay to examine social interactions in Drosophila and, as a first attempt, apply it here at examining the behavior of Drosophila Fragile X Mental Retardation gene (dfmr1) mutants. Fragile X syndrome is the most common cause of single gene intellectual disability (ID) and is frequently associated with autism. Our results suggest that dfmr1 mutants are less active than wild-type flies and interact with each other less often. In addition, mutants for one allele of dfmr1, dfmr1(B55), are more likely to come in close contact with a wild-type fly than another dfmr1(B55) mutant. Our results raise the possibility of defective social expression with preserved receptive abilities. We further suggest that the assay may be applied in a general strategy of examining endophenoypes of complex human neurological disorders in Drosophila, and specifically in order to understand the genetic basis of social interaction defects linked with ID.
我们开发了一种新的检测方法来研究果蝇的社交互动,并首次尝试将其用于检测果蝇脆性X智力低下基因(dfmr1)突变体的行为。脆性X综合征是单基因智力残疾(ID)最常见的病因,且常与自闭症相关。我们的结果表明,dfmr1突变体的活跃度低于野生型果蝇,且彼此之间的互动频率更低。此外,dfmr1的一个等位基因dfmr1(B55)的突变体比另一个dfmr1(B55)突变体更有可能与野生型果蝇密切接触。我们的结果提出了一种可能性,即社交表达存在缺陷但接受能力保留。我们进一步表明,该检测方法可应用于研究果蝇中复杂人类神经疾病内表型的一般策略,特别是为了了解与ID相关的社交互动缺陷的遗传基础。