Literature DB >> 1898730

Tyrosinases from two different loci are expressed by normal and by transformed melanocytes.

M Jiménez1, K Tsukamoto, V J Hearing.   

Abstract

Two pigmentation related genes have recently been cloned which map to the brown (b) and albino (c) loci of mice; these loci influence the quality and quantity, respectively, of melanin produced by melanocytes. Both these gene products are biochemically similar and have extensive amino acid sequence similarity to each other and to lower forms of tyrosinase (EC 1.14.18.1), a copper binding enzyme responsible for melanin production. In order to characterize the catalytic activities of these molecules, we have synthesized peptides and prepared antibodies to them which specifically recognize the gene products in question. By use of immune affinity purification protocols, we have isolated the proteins encoded by the brown and albino loci and have determined that both have the catalytic functions ascribed to tyrosinase, i.e. hydroxylation of tyrosine to 3,4-dihydroxyphenylalanine (DOPA) and the oxidation of DOPA to DOPAquinone. These are the critical reactions to melanogenesis since melanin pigment can be spontaneously produced from those products. The specific activity of the albino locus encoded product is considerably higher than that of the protein encoded by the brown locus, although the latter protein is present in higher quantity in melanocytes than is the protein encoded by the albino locus. These results are surprising since it was anticipated that tyrosinase was the product of single gene locus, and suggest that regulation of melanogenesis in mammals is controlled at the enzymatic level by several different gene products.

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Year:  1991        PMID: 1898730

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  46 in total

1.  Pink-eyed dilution protein controls the processing of tyrosinase.

Authors:  Kun Chen; Prashiela Manga; Seth J Orlow
Journal:  Mol Biol Cell       Date:  2002-06       Impact factor: 4.138

2.  Essential role of the molecular chaperone gp96 in regulating melanogenesis.

Authors:  Yongliang Zhang; Kristi L Helke; Sergio G Coelho; Julio C Valencia; Vincent J Hearing; Shaoli Sun; Bei Liu; Zihai Li
Journal:  Pigment Cell Melanoma Res       Date:  2013-10-09       Impact factor: 4.693

3.  Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 gene.

Authors:  P Manga; J G Kromberg; N F Box; R A Sturm; T Jenkins; M Ramsay
Journal:  Am J Hum Genet       Date:  1997-11       Impact factor: 11.025

4.  Rab8 regulates the actin-based movement of melanosomes.

Authors:  Marion L Chabrillat; Claire Wilhelm; Christina Wasmeier; Elena V Sviderskaya; Daniel Louvard; Evelyne Coudrier
Journal:  Mol Biol Cell       Date:  2005-01-26       Impact factor: 4.138

5.  A single base insertion in the putative transmembrane domain of the tyrosinase gene as a cause for tyrosinase-negative oculocutaneous albinism.

Authors:  C D Chintamaneni; R Halaban; Y Kobayashi; C J Witkop; B S Kwon
Journal:  Proc Natl Acad Sci U S A       Date:  1991-06-15       Impact factor: 11.205

6.  Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: a new subtype of albinism classified as "OCA3".

Authors:  R E Boissy; H Zhao; W S Oetting; L M Austin; S C Wildenberg; Y L Boissy; Y Zhao; R A Sturm; V J Hearing; R A King; J J Nordlund
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

7.  Beta-catenin activity in the dermal papilla of the hair follicle regulates pigment-type switching.

Authors:  David Enshell-Seijffers; Catherine Lindon; Eleanor Wu; Makoto M Taketo; Bruce A Morgan
Journal:  Proc Natl Acad Sci U S A       Date:  2010-11-22       Impact factor: 11.205

8.  L-tyrosine induces tyrosinase expression via a posttranscriptional mechanism.

Authors:  A Slominski; R Costantino
Journal:  Experientia       Date:  1991-07-15

9.  Changes in expression of putative antigens encoded by pigment genes in mouse melanomas at different stages of malignant progression.

Authors:  S J Orlow; V J Hearing; C Sakai; K Urabe; B K Zhou; W K Silvers; B Mintz
Journal:  Proc Natl Acad Sci U S A       Date:  1995-10-24       Impact factor: 11.205

10.  Identification of morc (microrchidia), a mutation that results in arrest of spermatogenesis at an early meiotic stage in the mouse.

Authors:  M L Watson; A R Zinn; N Inoue; K D Hess; J Cobb; M A Handel; R Halaban; C C Duchene; G M Albright; R W Moreadith
Journal:  Proc Natl Acad Sci U S A       Date:  1998-11-24       Impact factor: 11.205

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