24
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Identification of Genes Expressed in Hyperpigmented Skin using Meta-Analysis of Microarray Datasets

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      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

          More than 375 genes have been identified that are involved in regulating skin pigmentation, and those act during development, survival, differentiation and/or responses of melanocytes to the environment. Many of those genes have been cloned and disruptions of their functions are associated with various pigmentary diseases, however many remain to be identified. We have performed a series of microarray analyses of hyperpigmented compared to less pigmented skin to identify genes responsible for those differences. The rationale and goal for this study was to perform a meta-analysis on those microarray databases to identify genes that may be significantly involved in regulating skin phenotype either directly or indirectly that might not have been identified due to subtle differences by any of those individual studies alone. The meta-analysis demonstrates that 1,271 probes representing 921 genes are differentially expressed at significant levels in the 5 microarray datasets compared, which provides new insights into the variety of genes involved in determining skin phenotype. Immunohistochemistry was used to validate 2 of those markers at the protein level (TRIM63 and QPCT) and we discuss the possible functions of those genes in regulating skin physiology.

          Related collections

          Most cited references20

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

          Physiological factors that regulate skin pigmentation.

          More than 150 genes have been identified that affect skin color either directly or indirectly, and we review current understanding of physiological factors that regulate skin pigmentation. We focus on melanosome biogenesis, transport and transfer, melanogenic regulators in melanocytes, and factors derived from keratinocytes, fibroblasts, endothelial cells, hormones, inflammatory cells, and nerves. Enzymatic components of melanosomes include tyrosinase, tyrosinase-related protein 1, and dopachrome tautomerase, which depend on the functions of OA1, P, MATP, ATP7A, and BLOC-1 to synthesize eumelanins and pheomelanins. The main structural component of melanosomes is Pmel17/gp100/Silv, whose sorting involves adaptor protein 1A (AP1A), AP1B, AP2, and spectrin, as well as a chaperone-like component, MART-1. During their maturation, melanosomes move from the perinuclear area toward the plasma membrane. Microtubules, dynein, kinesin, actin filaments, Rab27a, melanophilin, myosin Va, and Slp2-a are involved in melanosome transport. Foxn1 and p53 up-regulate skin pigmentation via bFGF and POMC derivatives including alpha-MSH and ACTH, respectively. Other critical factors that affect skin pigmentation include MC1R, CREB, ASP, MITF, PAX3, SOX9/10, LEF-1/TCF, PAR-2, DKK1, SCF, HGF, GM-CSF, endothelin-1, prostaglandins, leukotrienes, thromboxanes, neurotrophins, and neuropeptides. UV radiation up-regulates most factors that increase melanogenesis. Further studies will elucidate the currently unknown functions of many other pigment genes/proteins. (c) 2009 International Union of Biochemistry and Molecular Biology, Inc.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: found
            Is Open Access

            Human pigmentation genes under environmental selection

            Genome-wide association studies and comparative genomics have established major loci and specific polymorphisms affecting human skin, hair and eye color. Environmental changes have had an impact on selected pigmentation genes as populations have expanded into different regions of the globe.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              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.
                Bookmark

                Author and article information

                Journal
                0426720
                4839
                J Invest Dermatol
                J. Invest. Dermatol.
                The Journal of investigative dermatology
                0022-202X
                1523-1747
                8 May 2015
                07 June 2015
                October 2015
                01 April 2016
                : 135
                : 10
                : 2455-2463
                Affiliations
                [1 ]Laboratory of Cell Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892 USA
                [2 ]R&D Skin Research, Beiersdorf AG, Hamburg 20245 Germany
                [3 ]Center for Devices and Radiological Health, Food and Drug Administration, Silver Spring, MD 20993, USA
                Author notes
                Correspondence to: Dr. Ludger Kolbe, R&D Skin Research, Beiersdorf AG, Hamburg 20245 Germany, Ludger.Kolbe@ 123456Beiersdorf.com
                Article
                NIHMS687603
                10.1038/jid.2015.179
                4567955
                25950827
                67f5e1d3-2902-4a7b-b386-b3b210380ac3

                Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms

                History
                Categories
                Article

                Dermatology
                Dermatology

                Comments

                Comment on this article