2007
DOI: 10.1073/pnas.0703247104
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Aryl hydrocarbon receptor nuclear translocator-like (BMAL1) is associated with susceptibility to hypertension and type 2 diabetes

Abstract: Many aspects of physiology and behavior follow a circadian rhythm. Brain and muscle Arnt-like protein-1 (BMAL1) is a key component of the mammalian molecular clock, which controls circadian oscillations. In the rat, the gene encoding Bmal1 is located within hypertension susceptibility loci. We analyzed the SNP distribution pattern in a congenic interval associated with hypertension in the spontaneously hypertensive rat (SHR), and we show that Bmal1 maps close to a region genetically divergent between SHR and i… Show more

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Cited by 350 publications
(261 citation statements)
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References 53 publications
(63 reference statements)
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“…That the mutation and genotypes of core clock genes are associated with metabolic diseases [15,[17][18][19] leads us to speculate that the circadian clock contributes to the development of diabetes. Oishi et al [29] demonstrated that clock function is preserved to a great extent in the livers, hearts and kidneys of mice with streptozotocininduced insulinopenic diabetes.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…That the mutation and genotypes of core clock genes are associated with metabolic diseases [15,[17][18][19] leads us to speculate that the circadian clock contributes to the development of diabetes. Oishi et al [29] demonstrated that clock function is preserved to a great extent in the livers, hearts and kidneys of mice with streptozotocininduced insulinopenic diabetes.…”
Section: Discussionmentioning
confidence: 99%
“…In addition, we showed that the rhythmic expression of clock genes is blunted in the liver and visceral adipose tissues of KK-A y mice, a genetic model of type 2 diabetes [16]. In humans, genetic variations in the BMAL1 gene (also known as ARNTL) are reported to be associated with susceptibility to type 2 diabetes and hypertension [17]. Furthermore, CLOCK haplotypes are associated with metabolic syndrome [18] and non-alcoholic fatty liver disease [19].…”
Section: Introductionmentioning
confidence: 94%
“…Genetic variations in human circadian clock genes have been associated with metabolic phenotypes. Haplotype analyses revealed that `il`h=gene polymorphisms are correlated with the development of metabolic syndrome, while certain _j^iN alleles are linked to type II diabetes and hypertension (Scott et al, 2007;Woon et al, 2007). These data propose that the transcription factors of the positive limb of the circadian clock may serve a protective role in the incidence of metabolic diseases.…”
Section: Circadian Control Of Metabolismmentioning
confidence: 93%
“…Rodents with clock gene mutations have dysfunctional glucose homeostasis, insulin secretion and sensitivity and fat and cholesterol metabolism (Rudic et al, 2004;Turek et al, 2005). Similarly, single nucleotide polymorphisms in Clock and Bmal1 genes in humans are associated with abnormal hepatic fat and glucose metabolism (Sookoian et al, 2007;Woon et al, 2007). …”
mentioning
confidence: 99%