The color loci of mice--a genetic century.

Color loci in mammals are those genetic loci in which mutations can affect pigmentation of the hair, skin, and/or eyes. In the mouse, over 800 phenotypic alleles are now known, at 127 identified color loci. As the number of color loci passed 100 only recently, we celebrate this 'century' with an overview of these loci, especially the 59 that have been cloned and sequenced. These fall into a number of functional groups representing melanocyte development and differentiation, melanosomal components, organelle biogenesis, organelle transport, control of pigment-type switching, and some systemic effects. A human ortholog has been identified in all cases, and the majority of these human genes are found to be loci for human disorders, often affecting other body systems as well as pigmentation. We expect that a significant number of color loci remain to be identified. Nonetheless, the large number known already provide a treasury of resources for reconstruction of the mechanisms, at the subcellular, cellular and tissue levels, that produce a functional pigmentary system and contribute to the normal development and functioning of many other organ systems. The mutant mice also provide valuable models for the study of human disease.

[1]  J. Garcia-conde,et al.  Nonmyeloablative transplantation with or without alemtuzumab: comparison between 2 prospective studies in patients with lymphoproliferative disorders. , 2002, Blood.

[2]  V. Hearing Biochemical control of melanogenesis and melanosomal organization. , 1999, The journal of investigative dermatology. Symposium proceedings.

[3]  I. Jackson,et al.  Identification of the albino mutation of mouse tyrosinase by analysis of an in vitro revertant. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[4]  W. Silvers The Coat Colors of Mice , 1979, Springer New York.

[5]  K. R. Fitch,et al.  Genetics of dark skin in mice. , 2003, Genes & development.

[6]  Kathleen J. Millen,et al.  The mouse Dreher gene Lmx1a controls formation of the roof plate in the vertebrate CNS , 2000, Nature.

[7]  David C. Lee,et al.  An essential role for ectodomain shedding in mammalian development. , 1998, Science.

[8]  N. Copeland,et al.  Interallelic complementation at the mouse Mitf locus. , 2003, Genetics.

[9]  J. McPherson,et al.  A defect in a novel ADAMTS family member is the cause of the belted white-spotting mutation , 2003, Development.

[10]  D. Provance,et al.  Melanophilin, the Product of the Leaden Locus, is Required for Targeting of Myosin‐Va to Melanosomes , 2002, Traffic.

[11]  K. Makino,et al.  Cloning and sequencing of mouse tyrosinase cDNA. , 1987 .

[12]  A. van Daal,et al.  Agouti: from mouse to man, from skin to fat. , 2002, Pigment cell research.

[13]  W. Pavan,et al.  Piebald lethal (sl) acts early to disrupt the development of neural crest-derived melanocytes. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[14]  P. Wangemann,et al.  KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential. , 2002, American journal of physiology. Cell physiology.

[15]  C. Petit,et al.  The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene , 1997, Nature Genetics.

[16]  V. McKusick Mendelian inheritance in man , 1971 .

[17]  J. Nordlund The pigmentary system : physiology and pathophysiology , 1998 .

[18]  D. Bennett,et al.  Effects of the developmental colour mutations silver and recessive spotting on proliferation of diploid and immortal mouse melanocytes in culture. , 1992, Development.

[19]  G. Raposo,et al.  Pmel17 initiates premelanosome morphogenesis within multivesicular bodies. , 2001, Molecular biology of the cell.

[20]  R. Spritz,et al.  Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[21]  G. Courtois,et al.  NEMO/IKK gamma-deficient mice model incontinentia pigmenti. , 2000, Molecular cell.

[22]  D. Bennett,et al.  The mouse silver locus encodes a single transcript truncated by the silver mutation , 1999, Mammalian Genome.

[23]  R. Boissy,et al.  Tyrp1 and oculocutaneous albinism type 3. , 2001, Pigment cell research.

[24]  Sridhar Ramaswamy,et al.  Bcl2 Regulation by the Melanocyte Master Regulator Mitf Modulates Lineage Survival and Melanoma Cell Viability , 2002, Cell.

[25]  L. Hou,et al.  Signaling and transcriptional regulation in the neural crest-derived melanocyte lineage: interactions between KIT and MITF. , 2000, Development.

[26]  J. Vacher,et al.  Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human , 2003, Nature Medicine.

[27]  T. Vogt,et al.  Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler (Va) mice , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[28]  G. Imokawa,et al.  Tyrosinase related protein 1 (TRP1) functions as a DHICA oxidase in melanin biosynthesis. , 1994, The EMBO journal.

[29]  J. Sellers,et al.  Rab27a is an essential component of melanosome receptor for myosin Va. , 2002, Molecular biology of the cell.

[30]  L. Collinson,et al.  The leaden Gene Product Is Required with Rab27a to Recruit Myosin Va to Melanosomes in Melanocytes , 2002, Traffic.

[31]  J. Bonifacino,et al.  Cappuccino, a mouse model of Hermansky-Pudlak syndrome, encodes a novel protein that is part of the pallidin-muted complex (BLOC-1). , 2003, Blood.

[32]  B. Kwon,et al.  Polymerization of 5,6-dihydroxyindole-2-carboxylic acid to melanin by the pmel 17/silver locus protein. , 1996, European journal of biochemistry.

[33]  C. Abbott,et al.  Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice , 2000, Nature Genetics.

[34]  B. Roe,et al.  The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 gene. , 2001, Genomics.

[35]  S. Orlow,et al.  Pink-eyed dilution protein modulates arsenic sensitivity and intracellular glutathione metabolism. , 2002, Molecular biology of the cell.

[36]  A. Órfão,et al.  Zinc-finger transcription factor Slug contributes to the function of the stem cell factor c-kit signaling pathway. , 2002, Blood.

[37]  G. Barsh From Agouti to Pomc—100 years of fat blonde mice , 1999, Nature Network Boston.

[38]  Stephen L. Johnson,et al.  How the zebrafish gets its stripes. , 2001, Developmental biology.

[39]  R. Spritz,et al.  Human and mouse disorders of pigmentation. , 2003, Current opinion in genetics & development.

[40]  K. von Figura,et al.  A di‐leucine‐based motif in the cytoplasmic tail of LIMP‐II and tyrosinase mediates selective binding of AP‐3 , 1998, The EMBO journal.

[41]  Janey L. Wiggs,et al.  Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice , 2002, Nature Genetics.

[42]  S. Klauck,et al.  Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium. , 2000, Nature.

[43]  A. Read,et al.  SLUG (SNAI2) deletions in patients with Waardenburg disease. , 2002, Human molecular genetics.

[44]  J. Kaplan,et al.  Chediak-Higashi Syndrome: a rare disorder of lysosomes and lysosome related organelles. , 2002, Pigment cell research.

[45]  S. Shibahara,et al.  Cloning and expression of cDNA encoding mouse tyrosinase. , 1986, Nucleic acids research.

[46]  H. Kerl,et al.  bcl‐2 Protein Expression in Cutaneous Malignant Melanoma and Benign Melanocytic Nevi , 1995, The American Journal of dermatopathology.

[47]  R. Nazarian,et al.  The molecular machinery for the biogenesis of lysosome-related organelles: lessons from Hermansky-Pudlak syndrome. , 2002, Seminars in cell & developmental biology.

[48]  M. L. Lamoreux Strain-specific white-spotting patterns in laboratory mice. , 1999, Pigment cell research.

[49]  J. Rashbass Online Mendelian Inheritance in Man. , 1995, Trends in genetics : TIG.

[50]  R. Spritz,et al.  A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinism. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[51]  C. Goding,et al.  Mitf from neural crest to melanoma: signal transduction and transcription in the melanocyte lineage. , 2000, Genes & development.

[52]  L. Yaswen,et al.  Obesity in the mouse model of pro-opiomelanocortin deficiency responds to peripheral melanocortin , 1999, Nature Medicine.

[53]  A. Takeda,et al.  Human oculocutaneous albinism caused by single base insertion in the tyrosinase gene. , 1989, Biochemical and biophysical research communications.

[54]  M. Marks,et al.  The melanosome: membrane dynamics in black and white , 2001, Nature Reviews Molecular Cell Biology.

[55]  B. Kwon,et al.  Isolation and sequence of a cDNA clone for human tyrosinase that maps at the mouse c-albino locus. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[56]  K. Sakaguchi,et al.  Identification of a human melanoma antigen recognized by tumor-infiltrating lymphocytes associated with in vivo tumor rejection. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[57]  M. Bittner,et al.  Mutation of melanosome protein RAB38 in chocolate mice , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[58]  Wei Li,et al.  Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene , 2002, Nature Genetics.

[59]  B. Kitchell,et al.  The biology of melanocytes. , 2003, Veterinary dermatology.

[60]  E. Price,et al.  MAP kinase links the transcription factor Microphthalmia to c-Kit signalling in melanocytes , 1998, Nature.

[61]  B. Roe,et al.  Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6 , 2003, Nature Genetics.

[62]  N. Andrews,et al.  A mutation in a mitochondrial transmembrane protein is responsible for the pleiotropic hematological and skeletal phenotype of flexed-tail (f/f) mice. , 2001, Genes & development.

[63]  R. Spritz,et al.  The Hermansky-Pudlak Syndrome 1 (HPS1) and HPS4 Proteins Are Components of Two Complexes, BLOC-3 and BLOC-4, Involved in the Biogenesis of Lysosome-related Organelles* , 2003, Journal of Biological Chemistry.

[64]  S. Orlow,et al.  Ocular albinism type 1: more than meets the eye. , 2001, Pigment cell research.

[65]  W. Gahl,et al.  Hermansky-Pudlak syndrome: vesicle formation from yeast to man. , 2002, Pigment cell research.

[66]  D. Bennett,et al.  The murine misty mutation: phenotypic effects on melanocytes, platelets and brown fat. , 1998, Genetics.

[67]  G. Barsh,et al.  Spongiform Degeneration in mahoganoid Mutant Mice , 2003, Science.

[68]  D. Bennett Genetics, development, and malignancy of melanocytes. , 1993, International review of cytology.