Literature DB >> 1924386

A melanocyte-specific gene, Pmel 17, maps near the silver coat color locus on mouse chromosome 10 and is in a syntenic region on human chromosome 12.

B S Kwon1, C Chintamaneni, C A Kozak, N G Copeland, D J Gilbert, N Jenkins, D Barton, U Francke, Y Kobayashi, K K Kim.   

Abstract

Melanocytes preferentially express an mRNA species, Pmel 17, whose protein product cross-reacts with anti-tyrosinase antibodies and whose expression correlates with the melanin content. We have now analyzed the deduced protein structure and mapped its chromosomal location in mouse and human. The amino acid sequence deduced from the nucleotide sequence of the Pmel 17 cDNA showed that the protein is composed of 645 amino acids with a molecular weight of 68,600. The Pmel 17 protein contains a putative leader sequence and a potential membrane anchor segment, which indicates that this may be a membrane-associated protein in melanocytes. The deduced protein contains five potential N-glycosylation sites and relatively high levels of serine and threonine. Three repeats of a 26-amino acid motif appear in the middle of the molecule. The human Pmel 17 gene, designated D12S53E, maps to chromosome 12, region 12pter-q21; and the mouse homologue, designated D12S53Eh, maps to the distal region of mouse chromosome 10, a region also known to carry the coat color locus si (silver).

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Year:  1991        PMID: 1924386      PMCID: PMC52687          DOI: 10.1073/pnas.88.20.9228

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  33 in total

Review 1.  Maps of linkage and synteny homologies between mouse and man.

Authors:  J H Nadeau
Journal:  Trends Genet       Date:  1989-03       Impact factor: 11.639

2.  Short related sequences in the cytoplasmic domains of CD4 and CD8 mediate binding to the amino-terminal domain of the p56lck tyrosine protein kinase.

Authors:  A S Shaw; J Chalupny; J A Whitney; C Hammond; K E Amrein; P Kavathas; B M Sefton; J K Rose
Journal:  Mol Cell Biol       Date:  1990-05       Impact factor: 4.272

3.  Detection of mutations in the tyrosinase gene in a patient with type IA oculocutaneous albinism.

Authors:  R A Spritz; K M Strunk; L B Giebel; R A King
Journal:  N Engl J Med       Date:  1990-06-14       Impact factor: 91.245

4.  In situ hybridization localizes the human putative oncogene GLI to chromosome subbands 12q13.3-14.1.

Authors:  K Arheden; M Rønne; N Mandahl; S Heim; K W Kinzler; B Vogelstein; F Mitelman
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

5.  Human oculocutaneous albinism caused by single base insertion in the tyrosinase gene.

Authors:  Y Tomita; A Takeda; S Okinaga; H Tagami; S Shibahara
Journal:  Biochem Biophys Res Commun       Date:  1989-11-15       Impact factor: 3.575

6.  undulated, a mutation affecting the development of the mouse skeleton, has a point mutation in the paired box of Pax 1.

Authors:  R Balling; U Deutsch; P Gruss
Journal:  Cell       Date:  1988-11-04       Impact factor: 41.582

7.  Localization of Evi-2 to chromosome 11: linkage to other proto-oncogene and growth factor loci using interspecific backcross mice.

Authors:  A M Buchberg; H G Bedigian; B A Taylor; E Brownell; J N Ihle; S Nagata; N A Jenkins; N G Copeland
Journal:  Oncogene Res       Date:  1988

8.  The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene.

Authors:  E N Geissler; M A Ryan; D E Housman
Journal:  Cell       Date:  1988-10-07       Impact factor: 41.582

9.  Fine mapping of a putative rd cDNA and its co-segregation with rd expression.

Authors:  M Danciger; C Bowes; C A Kozak; M M LaVail; D B Farber
Journal:  Invest Ophthalmol Vis Sci       Date:  1990-08       Impact factor: 4.799

10.  The melanoma antigen gp75 is the human homologue of the mouse b (brown) locus gene product.

Authors:  S Vijayasaradhi; B Bouchard; A N Houghton
Journal:  J Exp Med       Date:  1990-04-01       Impact factor: 14.307

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  47 in total

1.  Molecular mapping of epitopes on melanocyte-specific protein Pmel17 which are recognized by autoantibodies in patients with vitiligo.

Authors:  E H Kemp; E A Waterman; D J Gawkrodger; P F Watson; A P Weetman
Journal:  Clin Exp Immunol       Date:  2001-06       Impact factor: 4.330

2.  Pmel17 initiates premelanosome morphogenesis within multivesicular bodies.

Authors:  J F Berson; D C Harper; D Tenza; G Raposo; M S Marks
Journal:  Mol Biol Cell       Date:  2001-11       Impact factor: 4.138

3.  A novel splice variant of Pmel17 expressed by human melanocytes and melanoma cells lacking some of the internal repeats.

Authors:  Sarah E Nichols; Dawn C Harper; Joanne F Berson; Michael S Marks
Journal:  J Invest Dermatol       Date:  2003-10       Impact factor: 8.551

Review 4.  Sequences associated with human iris pigmentation.

Authors:  Tony Frudakis; Matthew Thomas; Zach Gaskin; K Venkateswarlu; K Suresh Chandra; Siva Ginjupalli; Sitaram Gunturi; Sivamani Natrajan; Viswanathan K Ponnuswamy; K N Ponnuswamy
Journal:  Genetics       Date:  2003-12       Impact factor: 4.562

Review 5.  Mouse chromosome 10.

Authors:  B A Taylor; W N Frankel; R H Reeves
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

6.  Repeat domains of melanosome matrix protein Pmel17 orthologs form amyloid fibrils at the acidic melanosomal pH.

Authors:  Ryan P McGlinchey; Frank Shewmaker; Kan-Nian Hu; Peter McPhie; Robert Tycko; Reed B Wickner
Journal:  J Biol Chem       Date:  2010-12-10       Impact factor: 5.157

7.  Effects of pH on aggregation kinetics of the repeat domain of a functional amyloid, Pmel17.

Authors:  Candace M Pfefferkorn; Ryan P McGlinchey; Jennifer C Lee
Journal:  Proc Natl Acad Sci U S A       Date:  2010-11-24       Impact factor: 11.205

Review 8.  Why Study Functional Amyloids? Lessons from the Repeat Domain of Pmel17.

Authors:  Ryan P McGlinchey; Jennifer C Lee
Journal:  J Mol Biol       Date:  2018-06-07       Impact factor: 5.469

Review 9.  Cytolytic T lymphocyte responses of cancer patients to tumor-associated antigens.

Authors:  P Romero
Journal:  Springer Semin Immunopathol       Date:  1996

10.  Mouse silver mutation is caused by a single base insertion in the putative cytoplasmic domain of Pmel 17.

Authors:  B S Kwon; R Halaban; S Ponnazhagan; K Kim; C Chintamaneni; D Bennett; R T Pickard
Journal:  Nucleic Acids Res       Date:  1995-01-11       Impact factor: 16.971

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