Genetic Differences in Human Circadian Clock Genes among Worldwide Populations

Author:

Ciarleglio Christopher M.1,Ryckman Kelli K.2,Servick Stein V.3,Hida Akiko3,Robbins Sam4,Wells Nancy4,Hicks Jennifer4,Larson Sydney A.3,Wiedermann Joshua P.3,Carver Krista4,Hamilton Nalo4,Kidd Kenneth K.5,Kidd Judith R.5,Smith Jeffrey R.2,Friedlaender Jonathan6,McMahon Douglas G.3,Williams Scott M.2,Summar Marshall L.7,Johnson Carl Hirschie8

Affiliation:

1. Department of Biological Sciences, Neuroscience Graduate Program, Vanderbilt University, Nashville, TN, USA

2. Department of Medicine and Center for Human Genetics Research, Vanderbilt University Medical Center, Nashville, TN, USA

3. Department of Biological Sciences, Vanderbilt University, Nashville, TN, USA

4. Vanderbilt University School of Nursing, Nashville, TN, USA

5. Department of Genetics, Yale University School of Medicine, New Haven, CT, USA

6. Department of Biological Anthropology (emeritus), Temple University, Philadelphia, PA, USA

7. Department of Pediatrics and Genetics, Vanderbilt University Medical Center, Nashville, TN, USA

8. Department of Biological Sciences, Vanderbilt University, Nashville, TN, USA,

Abstract

The daily biological clock regulates the timing of sleep and physiological processes that are of fundamental importance to human health, performance, and well-being. Environmental parameters of relevance to biological clocks include (1) daily fluctuations in light intensity and temperature, and (2) seasonal changes in photoperiod (day length) and temperature; these parameters vary dramatically as a function of latitude and locale. In wide-ranging species other than humans, natural selection has genetically optimized adaptiveness along latitudinal clines. Is there evidence for selection of clock gene alleles along latitudinal/photoperiod clines in humans? A number of polymorphisms in the human clock genes Per2, Per3, Clock, and AANAT have been reported as alleles that could be subject to selection. In addition, this investigation discovered several novel polymorphisms in the human Arntl and Arntl2 genes that may have functional impact upon the expression of these clock transcriptional factors. The frequency distribution of these clock gene polymorphisms is reported for diverse populations of African Americans, European Americans, Ghanaians, Han Chinese, and Papua New Guineans (including 5 subpopulations within Papua New Guinea). There are significant differences in the frequency distribution of clock gene alleles among these populations. Population genetic analyses indicate that these differences are likely to arise from genetic drift rather than from natural selection.

Publisher

SAGE Publications

Subject

Physiology (medical),Physiology

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