24
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      ARNTL ( BMAL1) and NPAS2 Gene Variants Contribute to Fertility and Seasonality

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background

          Circadian clocks guide the metabolic, cell-division, sleep-wake, circadian and seasonal cycles. Abnormalities in these clocks may be a health hazard. Circadian clock gene polymorphisms have been linked to sleep, mood and metabolic disorders. Our study aimed to examine polymorphisms in four key circadian clock genes in relation to seasonal variation, reproduction and well-being in a sample that was representative of the general population, aged 30 and over, living in Finland.

          Methodology/Principal Findings

          Single-nucleotide polymorphisms in the ARNTL, ARNTL2, CLOCK and NPAS2 genes were genotyped in 511 individuals. 19 variants were analyzed in relation to 31 phenotypes that were assessed in a health interview and examination study. With respect to reproduction, women with ARNTL rs2278749 TT genotype had more miscarriages and pregnancies, while NPAS2 rs11673746 T carriers had fewer miscarriages. NPAS2 rs2305160 A allele carriers had lower Global Seasonality Scores, a sum score of six items i.e. seasonal variation of sleep length, social activity, mood, weight, appetite and energy level. Furthermore, carriers of A allele at NPAS2 rs6725296 had greater loadings on the metabolic factor (weight and appetite) of the global seasonality score, whereas individuals with ARNTL rs6290035 TT genotype experienced less seasonal variation of energy level.

          Conclusions/Significance

          ARNTL and NPAS2 gene variants were associated with reproduction and with seasonal variation. Earlier findings have linked ARNTL to infertility in mice, but this is the first time when any polymorphism of these genes is linked to fertility in humans.

          Related collections

          Most cited references51

          • Record: found
          • Abstract: found
          • Article: not found

          The genetics of mammalian circadian order and disorder: implications for physiology and disease.

          Circadian cycles affect a variety of physiological processes, and disruptions of normal circadian biology therefore have the potential to influence a range of disease-related pathways. The genetic basis of circadian rhythms is well studied in model organisms and, more recently, studies of the genetic basis of circadian disorders has confirmed the conservation of key players in circadian biology from invertebrates to humans. In addition, important advances have been made in understanding how these molecules influence physiological functions in tissues throughout the body. Together, these studies set the scene for applying our knowledge of circadian biology to the understanding and treatment of a range of human diseases, including cancer and metabolic and behavioural disorders.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Molecular components of the mammalian circadian clock.

            Circadian rhythms are approximately 24-h oscillations in behavior and physiology, which are internally generated and function to anticipate the environmental changes associated with the solar day. A conserved transcriptional-translational autoregulatory loop generates molecular oscillations of 'clock genes' at the cellular level. In mammals, the circadian system is organized in a hierarchical manner, in which a master pacemaker in the suprachiasmatic nucleus (SCN) regulates downstream oscillators in peripheral tissues. Recent findings have revealed that the clock is cell-autonomous and self-sustained not only in a central pacemaker, the SCN, but also in peripheral tissues and in dissociated cultured cells. It is becoming evident that specific contribution of each clock component and interactions among the components vary in a tissue-specific manner. Here, we review the general mechanisms of the circadian clockwork, describe recent findings that elucidate tissue-specific expression patterns of the clock genes and address the importance of circadian regulation in peripheral tissues for an organism's overall well-being.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Early aging and age-related pathologies in mice deficient in BMAL1, the core componentof the circadian clock.

              Mice deficient in the circadian transcription factor BMAL1 (brain and muscle ARNT-like protein) have impaired circadian behavior and demonstrate loss of rhythmicity in the expression of target genes. Here we report that Bmal1(-/-) mice have reduced lifespans and display various symptoms of premature aging including sarcopenia, cataracts, less subcutaneous fat, organ shrinkage, and others. The early aging phenotype correlates with increased levels of reactive oxygen species in some tissues of the Bmal1(-/- )animals. These findings, together with data on CLOCK/BMAL1-dependent control of stress responses, may provide a mechanistic explanation for the early onset of age-related pathologies in the absence of BMAL1.
                Bookmark

                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2010
                2 April 2010
                : 5
                : 4
                : e10007
                Affiliations
                [1 ]Department of Mental Health and Substance Abuse Services, National Institute for Health and Welfare, Helsinki, Finland
                [2 ]Department of Alcohol, Drugs and Addiction, National Institute for Health and Welfare, Helsinki, Finland
                [3 ]Division of Welfare and Health Policies, National Institute for Health and Welfare, Helsinki, Finland
                [4 ]Department of Psychiatry, University of Helsinki, Helsinki, Finland
                Leiden University Medical Center, Netherlands
                Author notes

                Conceived and designed the experiments: STS AA JL TP. Performed the experiments: LK. Analyzed the data: LK. Contributed reagents/materials/analysis tools: STS AA JL TP. Wrote the paper: LK STS AA JL TP.

                Article
                09-PONE-RA-14919R1
                10.1371/journal.pone.0010007
                2848852
                20368993
                5d1958a0-cdd3-4a90-8ddb-0a30e340e551
                Kovanen et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 15 December 2009
                : 10 March 2010
                Page count
                Pages: 6
                Categories
                Research Article
                Mental Health
                Genetics and Genomics/Complex Traits
                Public Health and Epidemiology/Social and Behavioral Determinants of Health

                Uncategorized
                Uncategorized

                Comments

                Comment on this article