Nejvíce citovaný článek - PubMed ID 25637625
Expression of clock genes period and timeless in the central nervous system of the Mediterranean flour moth, Ephestia kuehniella
Drosophila melanogaster has served as an excellent genetic model to decipher the molecular basis of the circadian clock. Two key proteins, PERIOD (PER) and TIMELESS (TIM), are particularly well explored and a number of various arrhythmic, slow, and fast clock mutants have been identified in classical genetic screens. Interestingly, the free running period (tau, τ) is influenced by temperature in some of these mutants, whereas τ is temperature-independent in other mutant lines as in wild-type flies. This, so-called "temperature compensation" ability is compromised in the mutant timeless allele "ritsu" (tim rit ), and, as we show here, also in the tim blind allele, mapping to the same region of TIM. To test if this region of TIM is indeed important for temperature compensation, we generated a collection of new mutants and mapped functional protein domains involved in the regulation of τ and in general clock function. We developed a protocol for targeted mutagenesis of specific gene regions utilizing the CRISPR/Cas9 technology, followed by behavioral screening. In this pilot study, we identified 20 new timeless mutant alleles with various impairments of temperature compensation. Molecular characterization revealed that the mutations included short in-frame insertions, deletions, or substitutions of a few amino acids resulting from the non-homologous end joining repair process. Our protocol is a fast and cost-efficient systematic approach for functional analysis of protein-coding genes and promoter analysis in vivo. Interestingly, several mutations with a strong temperature compensation defect map to one specific region of TIM. Although the exact mechanism of how these mutations affect TIM function is as yet unknown, our in silico analysis suggests they affect a putative nuclear export signal (NES) and phosphorylation sites of TIM. Immunostaining for PER was performed on two TIM mutants that display longer τ at 25°C and complete arrhythmicity at 28°C. Consistently with the behavioral phenotype, PER immunoreactivity was reduced in circadian clock neurons of flies exposed to elevated temperatures.
- Klíčová slova
- CRISPR-CAS9, Drosophila melanogaster, candidate genes, circadian clock, reverse genetics, screening, temperature compensation,
- Publikační typ
- časopisecké články MeSH
Circadian clocks orchestrate daily activity patterns and free running periods of locomotor activity under constant conditions. While the first often depends on temperature, the latter is temperature-compensated over a physiologically relevant range. Here, we explored the locomotor activity of the temperate housefly Musca domestica Under low temperatures, activity was centered round a major and broad afternoon peak, while high temperatures resulted in activity throughout the photophase with a mild midday depression, which was especially pronounced in males exposed to long photoperiods. While period (per) mRNA peaked earlier under low temperatures, no temperature-dependent splicing of the last per 3' end intron was identified. The expression of timeless, vrille, and Par domain protein 1 was also influenced by temperature, each in a different manner. Our data indicated that comparable behavioral trends in daily activity distribution have evolved in Drosophila melanogaster and M. domestica, yet the behaviors of these two species are orchestrated by different molecular mechanisms.
- Klíčová slova
- circadian clock genes, locomotor activity, mRNA splicing, temperature compensation of circadian rhythms, transcription,
- MeSH
- 3' nepřekládaná oblast genetika MeSH
- časové faktory MeSH
- cirkadiánní rytmus genetika MeSH
- Drosophila melanogaster genetika MeSH
- exony genetika MeSH
- fotoperioda MeSH
- fylogeneze MeSH
- hmyzí geny * MeSH
- introny genetika MeSH
- kondiční příprava zvířat MeSH
- kryptochromy genetika MeSH
- messenger RNA genetika metabolismus MeSH
- moucha domácí MeSH
- pohybová aktivita MeSH
- promotorové oblasti (genetika) genetika MeSH
- regulace genové exprese MeSH
- sestřih RNA genetika MeSH
- teplota * MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 3' nepřekládaná oblast MeSH
- kryptochromy MeSH
- messenger RNA MeSH