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Chronic jetlag-induced alterations in pancreatic diurnal gene expression.
Schwartz, Patrick B; Walcheck, Morgan T; Berres, Mark; Nukaya, Manabu; Wu, Gang; Carrillo, Noah D; Matkowskyj, Kristina A; Ronnekleiv-Kelly, Sean M.
Affiliation
  • Schwartz PB; Division of Surgical Oncology, Department of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
  • Walcheck MT; Division of Surgical Oncology, Department of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
  • Berres M; Biotechnology Center, University of Wisconsin, Madison, Wisconsin.
  • Nukaya M; Division of Surgical Oncology, Department of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
  • Wu G; Division of Human Genetics and Immunobiology, Center for Chronobiology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Carrillo ND; Division of Surgical Oncology, Department of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
  • Matkowskyj KA; Department of Pathology and Laboratory Medicine, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
  • Ronnekleiv-Kelly SM; University of Wisconsin Carbone Cancer Center, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
Physiol Genomics ; 53(8): 319-335, 2021 08 01.
Article in En | MEDLINE | ID: mdl-34056925
ABSTRACT
Cell-autonomous circadian clocks exist in nearly every organ and function to maintain homeostasis through a complex series of transcriptional-translational feedback loops. The response of these peripheral clocks to external perturbations, such as chronic jetlag and shift work, has been extensively investigated. However, an evaluation of the effects of chronic jetlag on the mouse pancreatic transcriptome is still lacking. Herein, we report an evaluation of the diurnal variations encountered in the pancreatic transcriptome following exposure to an established chronic jetlag protocol. We found approximately 5.4% of the pancreatic transcriptome was rhythmic. Following chronic jetlag, we found the number of rhythmic transcripts decreased to approximately 3.6% of the transcriptome. Analysis of the core clock genes, which orchestrate circadian physiology, revealed that nearly all exhibited a shift in the timing of peak gene expression-known as a phase shift. Similarly, over 95% of the rhythmically expressed genes in the pancreatic transcriptome exhibited a phase shift, many of which were found to be important for metabolism. Evaluation of the genes involved in pancreatic exocrine secretion and insulin signaling revealed many pancreas-specific genes were also rhythmically expressed and several displayed a concomitant phase shift with chronic jetlag. Phase differences were found 9 days after normalization, indicating a persistent failure to reentrain to the new light-dark cycle. This study is the first to evaluate the endogenous pancreatic clock and rhythmic gene expression in whole pancreas over 48 h, and how the external perturbation of chronic jetlag affects the rhythmic expression of genes in the pancreatic transcriptome.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancreas / Gene Expression Regulation / Circadian Rhythm / Jet Lag Syndrome Limits: Animals Language: En Journal: Physiol Genomics Journal subject: BIOLOGIA MOLECULAR Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancreas / Gene Expression Regulation / Circadian Rhythm / Jet Lag Syndrome Limits: Animals Language: En Journal: Physiol Genomics Journal subject: BIOLOGIA MOLECULAR Year: 2021 Document type: Article