TY - JOUR
T1 - Long-term effect of systemic RNA interference on circadian clock genes in hemimetabolous insects
AU - Uryu, Outa
AU - Kamae, Yuichi
AU - Tomioka, Kenji
AU - Yoshii, Taishi
N1 - Funding Information:
We thank Christa Kistenpfennig for helpful comments on the manuscript. We also thank Moe Miyamoto for the graphical abstract. This work was partly supported by research grants from Grants-in-Aid for Scientific Research (KAKENHI 23870021 to T.Y. and KAKENHI 23657056 to K.T.). O.U. and Y.K. are supported by Grants-in-Aid for JSPS Fellows.
PY - 2013/4
Y1 - 2013/4
N2 - RNA interference (RNAi) strategy, which enables gene-specific knock-down of transcripts, has been spread across a wide area of insect studies for investigating gene function without regard to model and non-model insects. This technique is of particular benefit to promote molecular studies on non-model insects. However, the optimal conditions for RNAi are still not well understood because of its variable efficiency depending on the species, target genes, and experimental conditions. To apply RNAi technique to long-running experiments such as chronobiological studies, the effects of RNAi have to persist throughout the experiment. In this study, we attempted to determine the optimal concentration of double-stranded RNA (dsRNA) for systemic RNAi and its effective period in two different insect species, the cricket Gryllus bimaculatus and the firebrat Thermobia domestica. In both species, higher concentrations of dsRNA principally yielded a more efficient knock-down of mRNA levels of tested clock genes, although the effect depended on the gene and the species. Surprisingly, the effect of the RNAi reached its maximum effect 1-2. weeks and 1. month after the injection of dsRNA in the crickets and the firebrats, respectively, suggesting a slow but long-term effect of RNAi. Our study provides fundamental information for utilizing RNAi technique in any long-running experiment.
AB - RNA interference (RNAi) strategy, which enables gene-specific knock-down of transcripts, has been spread across a wide area of insect studies for investigating gene function without regard to model and non-model insects. This technique is of particular benefit to promote molecular studies on non-model insects. However, the optimal conditions for RNAi are still not well understood because of its variable efficiency depending on the species, target genes, and experimental conditions. To apply RNAi technique to long-running experiments such as chronobiological studies, the effects of RNAi have to persist throughout the experiment. In this study, we attempted to determine the optimal concentration of double-stranded RNA (dsRNA) for systemic RNAi and its effective period in two different insect species, the cricket Gryllus bimaculatus and the firebrat Thermobia domestica. In both species, higher concentrations of dsRNA principally yielded a more efficient knock-down of mRNA levels of tested clock genes, although the effect depended on the gene and the species. Surprisingly, the effect of the RNAi reached its maximum effect 1-2. weeks and 1. month after the injection of dsRNA in the crickets and the firebrats, respectively, suggesting a slow but long-term effect of RNAi. Our study provides fundamental information for utilizing RNAi technique in any long-running experiment.
KW - Clock gene
KW - Cricket
KW - Double-stranded RNA
KW - Firebrat
KW - Gene knock-down
KW - RNA interference
UR - http://www.scopus.com/inward/record.url?scp=84875518176&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84875518176&partnerID=8YFLogxK
U2 - 10.1016/j.jinsphys.2013.02.009
DO - 10.1016/j.jinsphys.2013.02.009
M3 - Article
C2 - 23458340
AN - SCOPUS:84875518176
SN - 0022-1910
VL - 59
SP - 494
EP - 499
JO - Journal of Insect Physiology
JF - Journal of Insect Physiology
IS - 4
ER -