Reynolds Julie A, Waight Emma M
Department of Evolution, Ecology, and Organismal Biolog, The Ohio State University, Columbus, OH 43210, United States.
Hablitz/Nedergaard Lab, Center for Translational Neuromedicine, University of Rochester Medical Center. Rochester, NY 14642, United States.
Curr Res Insect Sci. 2024 Sep 26;6:100099. doi: 10.1016/j.cris.2024.100099. eCollection 2024.
The maternal regulation of diapause is one type of phenotypic plasticity where the experience of the mother leads to changes in the phenotype of her offspring that impact how well-suited they will be to their future environment. females with a diapause history produce offspring that cannot enter diapause even if they are reared in a diapause inducing environment. Accumulating evidence suggests that microRNAs regulate diapause and, possibly, maternal regulation of diapause. We found significant differences in the abundances of several microRNAs (miR-125-5p, miR-124-3p, miR-31-5p, and miR-277-3p) in brains dissected from adult female that had experienced diapause compared to females with no diapause history. We also found moderate differences in the mRNA expression of the circadian-clock related genes, and . MiR-124-3p and miR-31-5p are part of a gene network that includes these circadian clock-related genes. Taken together our results suggest the maternal block of diapause in is regulated, at least in part, by a network that includes microRNAs and the circadian clock.
母体对滞育的调控是一种表型可塑性,即母体的经历会导致其后代的表型发生变化,从而影响后代对未来环境的适应程度。有滞育经历的雌性产生的后代即使在诱导滞育的环境中饲养也无法进入滞育状态。越来越多的证据表明,微小RNA调控滞育,并且可能调控母体对滞育的调控。我们发现,与没有滞育经历的雌性相比,从经历过滞育的成年雌性解剖出的大脑中,几种微小RNA(miR-125-5p、miR-124-3p、miR-31-5p和miR-277-3p)的丰度存在显著差异。我们还发现,生物钟相关基因和的mRNA表达存在适度差异。MiR-124-3p和miR-31-5p是一个基因网络的一部分,该基因网络包括这些生物钟相关基因。综合我们的结果表明,[具体物种名称]中母体对滞育的阻断至少部分受一个包括微小RNA和生物钟的网络调控。