PT  - JOURNAL ARTICLE
AU  - Boil Kim
AU  - Jihoon Kim
AU  - Minjeong Chun
AU  - Inah Park
AU  - Mijung Choi
AU  - Kyungjin Kim
AU  - Han Kyoung Choe
TI  - Single adeno-associated virus-based multiplexed CRISPR-Cas9 system to nullify core components of the mammalian molecular clock
AID  - 10.1101/2020.07.02.184119
DP  - 2020 Jan 01
TA  - bioRxiv
PG  - 2020.07.02.184119
4099  - http://biorxiv.org/content/early/2020/07/03/2020.07.02.184119.short
4100  - http://biorxiv.org/content/early/2020/07/03/2020.07.02.184119.full
AB  - The mammalian molecular clock is based on a transcription-translation feedback loop (TTFL) containing Period1, 2 (Per1, 2), Cryptochrome1, 2 (Cry1, 2), and Brain and Muscle ARNT-Like 1 (Bmal1). TTFL robustness is endowed by genetic complementation between these components; therefore, multiple genes must be knocked out to physiologically investigate the molecular clock, which requires extensive research resources. To facilitate molecular clock disruption, we developed a CRISPR-Cas9-based single adeno-associated viral (AAV) system targeting the circadian clock (CSAC) for Pers, Crys, or Bmal1. First, we designed single guide RNAs (sgRNAs) targeting individual clock genes using an in silico approach and validated their efficiency in Neuro2a cells. To target multiple genes, multiplex sgRNA plasmids were constructed using Golden Gate assembly and expressed in viral vectors. CSAC efficiency was demonstrated by decreased protein expression in vitro and ablated molecular oscillation ex vivo. We also measured locomotor activity and body temperature in Cas9-expressing mice injected with CSAC at the suprachiasmatic nucleus. Circadian rhythm disruption was observed under free-running conditions, indicating that CSAC can efficiently and robustly disrupt molecular circadian clock. Thus, CSAC is a simple and powerful tool for investigating the physiological role of the molecular clock in vivo.Competing Interest StatementThe authors have declared no competing interest.