Literature DB >> 16199032

Heterologous expression of tyrosinase recapitulates the misprocessing and mistrafficking in oculocutaneous albinism type 2: effects of altering intracellular pH and pink-eyed dilution gene expression.

Li Ni-Komatsu1, Seth J Orlow.   

Abstract

The processing and trafficking of tyrosinase, a melanosomal protein essential for pigmentation, was investigated in a human epithelial 293 cell line that stably expresses the protein. The effects of the pink-eyed dilution (p) gene product, in which mutations result in oculocutaneous albinism type 2 (OCA2), on the processing and trafficking of tyrosinase in this cell line were studied. The majority of tyrosinase was retained in the endoplasmic reticulum-Golgi intermediate compartment and the early Golgi compartment in the 293 cells expressing the protein. Coexpression of p could partially correct the mistrafficking of tyrosinase in 293 cells. Tyrosinase was targeted to the late endosomal and lysosomal compartments after treatment of the cells with compounds that correct the tyrosinase mistrafficking in albino melanocytes, most likely through altering intracellular pH, while the substrate tyrosine had no effect on the processing of tyrosinase. Remarkably, this heterologous expression system recapitulates the defective processing and mistrafficking of tyrosinase observed in OCA2 albino melanocytes and certain amelanotic melanoma cells. Coexpression of other melanosomal proteins in this heterologous system may further aid our understanding of the details of normal and pathologic processing of melanosomal proteins.

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Year:  2005        PMID: 16199032     DOI: 10.1016/j.exer.2005.08.013

Source DB:  PubMed          Journal:  Exp Eye Res        ISSN: 0014-4835            Impact factor:   3.467


  12 in total

Review 1.  Oculocutaneous albinism: epidemiology, genetics, skin manifestation, and psychosocial issues.

Authors:  Emily Z Ma; Albert E Zhou; Karl M Hoegler; Amor Khachemoune
Journal:  Arch Dermatol Res       Date:  2022-02-25       Impact factor: 3.017

2.  A community-science approach identifies genetic variants associated with three color morphs in ball pythons (Python regius).

Authors:  Autumn R Brown; Kaylee Comai; Dominic Mannino; Haily McCullough; Yamini Donekal; Hunter C Meyers; Chiron W Graves; Hannah S Seidel
Journal:  PLoS One       Date:  2022-10-19       Impact factor: 3.752

3.  Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus).

Authors:  Rebecca R Bellone; Samantha A Brooks; Lynne Sandmeyer; Barbara A Murphy; George Forsyth; Sheila Archer; Ernest Bailey; Bruce Grahn
Journal:  Genetics       Date:  2008-07-27       Impact factor: 4.562

4.  Pigmentation in Black-boned sheep (Ovis aries): association with polymorphism of the MC1R gene.

Authors:  W D Deng; W Shu; S L Yang; X W Shi; H M Mao
Journal:  Mol Biol Rep       Date:  2007-12-13       Impact factor: 2.316

5.  Pigmented-MDCK (P-MDCK) cell line with tunable melanin expression: an in vitro model for the outer blood-retinal barrier.

Authors:  Rajendra S Kadam; Robert I Scheinman; Uday B Kompella
Journal:  Mol Pharm       Date:  2012-10-15       Impact factor: 4.939

Review 6.  Ion transport in pigmentation.

Authors:  Nicholas W Bellono; Elena V Oancea
Journal:  Arch Biochem Biophys       Date:  2014-07-14       Impact factor: 4.013

Review 7.  [Phenotype of the visual system in oculocutaneous and ocular albinism].

Authors:  B Käsmann-Kellner; B Seitz
Journal:  Ophthalmologe       Date:  2007-08       Impact factor: 1.059

Review 8.  [Oculocutaneous and ocular albinism].

Authors:  A S Kubasch; M Meurer
Journal:  Hautarzt       Date:  2017-11       Impact factor: 0.751

9.  An intracellular anion channel critical for pigmentation.

Authors:  Nicholas W Bellono; Iliana E Escobar; Ariel J Lefkovith; Michael S Marks; Elena Oancea
Journal:  Elife       Date:  2014-12-16       Impact factor: 8.140

Review 10.  Oculocutaneous albinism.

Authors:  Karen Grønskov; Jakob Ek; Karen Brondum-Nielsen
Journal:  Orphanet J Rare Dis       Date:  2007-11-02       Impact factor: 4.123

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