Integrated RNA-seq Analysis Indicates Asynchrony in Clock Genes between Tissues under Spaceflight.
Shin-Ichiro FujitaLindsay RutterQuang OngMasafumi MurataniPublished in: Life (Basel, Switzerland) (2020)
Rodent models have been widely used as analogs for estimating spaceflight-relevant molecular mechanisms in human tissues. NASA GeneLab provides access to numerous spaceflight omics datasets that can potentially generate novel insights and hypotheses about fundamental space biology when analyzed in new and integrated fashions. Here, we performed a pilot study to elucidate space biological mechanisms across tissues by reanalyzing mouse RNA-sequencing spaceflight data archived on NASA GeneLab. Our results showed that clock gene expressions in spaceflight mice were altered compared with those in ground control mice. Furthermore, the results suggested that spaceflight promotes asynchrony of clock gene expressions between peripheral tissues. Abnormal circadian rhythms are associated not only with jet lag and sleep disorders but also with cancer, lifestyle-related diseases, and mental disorders. Overall, our findings highlight the importance of elucidating the causes of circadian rhythm disruptions using the unique approach of space biology research to one day potentially develop countermeasures that benefit humans on Earth and in space.
Keyphrases
- rna seq
- single cell
- gene expression
- genome wide
- genome wide identification
- endothelial cells
- copy number
- metabolic syndrome
- cardiovascular disease
- high fat diet induced
- heart rate
- squamous cell carcinoma
- dna methylation
- genome wide analysis
- type diabetes
- depressive symptoms
- wild type
- data analysis
- induced pluripotent stem cells
- artificial intelligence