The search for circadian clock components in humans: new perspectives for association studies

被引:53
作者
Allebrandt, K. V. [1 ]
Roenneberg, T. [1 ]
机构
[1] Univ Munich, Inst Med Psychol, Ctr Chronobiol, D-80336 Munich, Germany
关键词
human clock genes; chronotype; morningness/eveningness; association studies; latitudinal hypothesis;
D O I
10.1590/S0100-879X2008000800013
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Individual circadian clocks entrain differently to environmental cycles (zeitgebers, e. g., light and darkness), earlier or later within the day, leading to different chronotypes. In human populations, the distribution of chronotypes forms a bell-shaped curve, with the extreme early and late types - larks and owls, respectively - at its ends. Human chronotype, which can be assessed by the timing of an individual's sleep-wake cycle, is partly influenced by genetic factors - known from animal experimentation. Here, we review population genetic studies which have used a questionnaire probing individual daily timing preference for associations with polymorphisms in clock genes. We discuss their inherent limitations and suggest an alternative approach combining a short questionnaire (Munich ChronoType Questionnaire, MCTQ), which assesses chronotype in a quantitative manner, with a genome-wide analysis (GWA). The advantages of these methods in comparison to assessing time-of-day preferences and single nucleotide polymorphism genotyping are discussed. In the future, global studies of chronotype using the MCTQ and GWA may also contribute to understanding the influence of seasons, latitude ( e. g., different photoperiods), and climate on allele frequencies and chronotype distribution in different populations.
引用
收藏
页码:716 / 721
页数:6
相关论文
共 55 条
[1]   Variability of the paraoxonase gene (PON1) in Euro- and Afro-Brazilians [J].
Allebrandt, KV ;
Souza, RLR ;
Chautard-Freire-Maia, EA .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2002, 180 (03) :151-156
[2]   A length polymorphism in the circadian clock gene Per3 is linked to delayed sleep phase syndrome and extreme diurnal preference [J].
Archer, SN ;
Robilliard, DL ;
Skene, DJ ;
Smits, M ;
Williams, A ;
Arendt, J ;
von Schantz, M .
SLEEP, 2003, 26 (04) :413-415
[3]  
ASCHOFF J, 1981, HDB BEHAVIORAL NEURO, P475
[4]   Differential functions of mPer1, mPer2, and mPer3 in the SCN circadian clock [J].
Bae, K ;
Jin, XW ;
Maywood, ES ;
Hastings, MH ;
Reppert, SM ;
Weaver, DR .
NEURON, 2001, 30 (02) :525-536
[5]   The period length of fibroblast circadian gene expression varies widely among human individuals [J].
Brown, SA ;
Fleury-Olela, F ;
Nagoshi, E ;
Hauser, C ;
Juge, C ;
Meier, CA ;
Chicheportiche, R ;
Dayer, JM ;
Albrecht, U ;
Schibler, U .
PLOS BIOLOGY, 2005, 3 (10) :1813-1818
[6]   Mop3 is an essential component of the master circadian pacemaker in mammals [J].
Bunger, MK ;
Wilsbacher, LD ;
Moran, SM ;
Clendenin, C ;
Radcliffe, LA ;
Hogenesch, JB ;
Simon, MC ;
Takahashi, JS ;
Bradfield, CA .
CELL, 2000, 103 (07) :1009-1017
[7]   A silent polymorphism in the PER1 gene associates with extreme diurnal preference in humans [J].
Carpen, Jayshan D. ;
von Schantz, Malcolm ;
Smits, Marcel ;
Skene, Debra J. ;
Archer, Simon N. .
JOURNAL OF HUMAN GENETICS, 2006, 51 (12) :1122-1125
[8]   A single-nucleotide polymorphism in the 5′-untranslated region of the hPER2 gene is associated with diurnal preference [J].
Carpen, JD ;
Archer, SN ;
Skene, DJ ;
Smits, M ;
von Schantz, M .
JOURNAL OF SLEEP RESEARCH, 2005, 14 (03) :293-297
[9]   A LATITUDINAL CLINE IN A DROSOPHILA CLOCK GENE [J].
COSTA, R ;
PEIXOTO, AA ;
BARBUJANI, G ;
KYRIACOU, CP .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1992, 250 (1327) :43-49
[10]   LIGHT-INDUCED RESETTING OF A CIRCADIAN CLOCK IS MEDIATED BY A RAPID INCREASE IN FREQUENCY TRANSCRIPT [J].
CROSTHWAITE, SK ;
LOROS, JJ ;
DUNLAP, JC .
CELL, 1995, 81 (07) :1003-1012