Abstract
Genetics is behind our circadian machinery. Some of our chronobiological characteristics could be influenced by genes. Different psychological traits such as depression, bipolar disorders, anxiety and seasonal variations of mood are intrinsically connected to chronobiology through different genetic variants. Moreover, sleep disorders or short sleep duration, are both associated to several polymorphisms connected to obesity. In this regards, one of the most outstanding SNPs is the CLOCK 3111TC SNP which is significantly associated to short sleep duration, eveningness, several psychological traits and obesity. This SNP has been also related to a reduction in weight loss effectiveness in patients submitted to a behavioral treatment of obesity. Ghrelin, eveningness, and a lack of compliance to the Mediterranean diet habits, could be behind these results. Apart from CLOCK SNPs, others genetic variants in several clock genes such as PERIOD or BMAL1 are also connected to obesity. The novel knowledge achieved in the circadian epigenome could give us new answers to the connections among genetics, circadian rhythmicity and obesity.
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- SNP:
-
Single nucleotide polymorphism
- CLOCK:
-
Circadian locomotor output cycles kaput
- PER:
-
Period homolog 2 (Drosophila)
- BMAL1 or ARNTL or MOP3:
-
Aryl hydrocarbon receptor nuclear translocator-like
- HGP:
-
Human genome project
- DNA:
-
Deoxyribonucleic acid
- RNA:
-
Ribonucleic acid
- mRNA:
-
Messenger ribonucleic acid
- GH:
-
Growth hormone
- SCN:
-
Suprachiasmatic nucleus
- MetS:
-
Metabolic syndrome
- MD:
-
Mood disorders
- OMIM:
-
Online Mendelian inheritance in man
- CRY:
-
Cryptochrome
- REV-ERBα:
-
Nuclear receptor Rev-ErbA-alpha
- SIRT:
-
Sirtuin
- RORA or NR1D1:
-
RAR-related orphan receptor A
- VIP:
-
Vasoactive intestinal polypeptide
- ROR1:
-
Receptor tyrosine kinase-like orphan receptor 1
- PLCB1:
-
Phospholipase C, beta 1
- OSAS:
-
Obstructive sleep apnea syndrome
- MTNR1A:
-
Melatonin receptor 1A
- MTNR1B:
-
Melatonin receptor 1B
- GWAS:
-
Genome-wide association studies
- NFATC2:
-
Nuclear factor of activated T cells 2
- SCP2:
-
Sterol carrier protein 2
- CACNA1C:
-
Calcium channel, voltage-dependent, L type, alpha 1C subunit
- TCRA:
-
T cell receptor alpha chain
- POLE:
-
Polymerase (DNA directed), epsilon
- FAM3D:
-
Family with sequence similarity 3, member D
- ABCC9:
-
ATP-binding cassette, sub-family C (CFTR/MRP), member 9
- SUR2:
-
Potential sterol desaturase similar to S. cerevisiae
- HLA:
-
Human leukocyte antigen
- DQB1:
-
Major histocompatibility complex, class II, DQ beta 1
- PSD:
-
Partial sleep deprivation
- NPAS2:
-
Neuronal PAS domain protein 2
- APSS:
-
Associated Professional Sleep Societies LLC
- FTO:
-
Fat mass and obesity associated
- HOMA-IR:
-
Homeostasis model assessment- insulin resistance
- TMEM18:
-
Transmembrane protein 18
- NRXN3:
-
Neurexin 3
- BMI:
-
Body mass index
- GOLDN:
-
Genetics of Lipids Lowering Drugs and Diet Network
- FAs:
-
Fatty acids
- MUFA:
-
Monounsaturated fatty acid
- SFA:
-
Saturated fatty acid
- MCP1:
-
Monocyte chemoattractant protein 1
- IL-6:
-
Interleukin 6
- PTMs:
-
Post translational modifications
- HAT:
-
Histone acetile transferase
- BMI:
-
Body mass index
- SAT:
-
Saturated fatty acids
- MUFA:
-
Monounsaturated fatty acids
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Garaulet, M., Ordovás, J.M. (2013). Genetics in Chronobiology and Obesity. In: Garaulet, M., Ordovás, J. (eds) Chronobiology and Obesity. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-5082-5_8
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