Migraine Genetics – A Review: Part I

Significant progress in molecular genetics has advanced our understanding of the genetic basis of migraine. The fundamentals of molecular genetics, and the recent advances in the field, are important for clinicians to understand, as they provide a foundation for critical appraisal of the literature, unprecedented insights into the pathogenesis of the disorder, and reveal promising treatment targets for future drug development. This paper provides a primer of molecular genetics and will be followed by a companion paper on the genetic advances in migraine, the methodology of genome wide association studies, and the potential clinical implications.

[1]  N. Fedoroff Transposable Elements, Epigenetics, and Genome Evolution , 2012 .

[2]  Rappold,et al.  Human Molecular Genetics , 1996, Nature Medicine.

[3]  Michael J Ackerman,et al.  Primer on medical genomics. Part VI: Genomics and molecular genetics in clinical practice. , 2003, Mayo Clinic proceedings.

[4]  L. Janusek,et al.  Epigenetics and psychoneuroimmunology: Mechanisms and models , 2011, Brain, Behavior, and Immunity.

[5]  Bronwen L. Aken,et al.  GENCODE: The reference human genome annotation for The ENCODE Project , 2012, Genome research.

[6]  T. Kouzarides Chromatin Modifications and Their Function , 2007, Cell.

[7]  Shane J. Neph,et al.  Systematic Localization of Common Disease-Associated Variation in Regulatory DNA , 2012, Science.

[8]  E. Pennisi Genomics. ENCODE project writes eulogy for junk DNA. , 2012, Science.

[9]  Fumiaki Sato,et al.  MicroRNAs and epigenetics , 2011, The FEBS journal.

[10]  E. Wieben,et al.  Primer on medical genomics part II: Background principles and methods in molecular genetics. , 2002, Mayo Clinic proceedings.

[11]  Teri A Manolio,et al.  Genomewide association studies and assessment of the risk of disease. , 2010, The New England journal of medicine.

[12]  D. S. Gross,et al.  Nuclease hypersensitive sites in chromatin. , 1988, Annual review of biochemistry.

[13]  M. Mehler,et al.  Emerging roles of non-coding RNAs in brain evolution, development, plasticity and disease , 2012, Nature Reviews Neuroscience.

[14]  Yi Dai,et al.  Up-regulation of platelet-activating factor synthases and its receptor in spinal cord contribute to development of neuropathic pain following peripheral nerve injury , 2012, Molecular pain.

[15]  N. Fedoroff Presidential address. Transposable elements, epigenetics, and genome evolution. , 2012, Science.

[16]  R. Fillingim,et al.  Chronic pain, perceived stress, and cellular aging: an exploratory study , 2012, Molecular pain.

[17]  Howard Y. Chang,et al.  Molecular mechanisms of long noncoding RNAs. , 2011, Molecular cell.

[18]  Jeannie T. Lee,et al.  X-Inactivation, Imprinting, and Long Noncoding RNAs in Health and Disease , 2013, Cell.

[19]  G. Dewald,et al.  Primer on medical genomics. Part XI: Visualizing human chromosomes. , 2004, Mayo Clinic proceedings.

[20]  E. Blackburn,et al.  Telomeres and telomerase. , 2002, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[21]  Francis S. Collins,et al.  Genomic medicine--a primer. , 2002, The New England journal of medicine.

[22]  P. Montagna The primary headaches: genetics, epigenetics and a behavioural genetic model , 2008, The Journal of Headache and Pain.

[23]  P. Zamore,et al.  Argonaute proteins , 2011, Current Biology.

[24]  P. Zamore,et al.  Small silencing RNAs: an expanding universe , 2009, Nature Reviews Genetics.

[25]  Leland H. Hartwell,et al.  Genetics: From Genes to Genomes , 1999 .

[26]  Elizabeth Pennisi,et al.  The Biology of Genomes. Disease risk links to gene regulation. , 2011, Science.

[27]  Hiroyuki Miyoshi,et al.  Self-formation of functional adenohypophysis in three-dimensional culture , 2011, Nature.

[28]  D. Tester,et al.  Primer on medical genomics. Part VIII: Essentials of medical genetics for the practicing physician. , 2003, Mayo Clinic proceedings.