Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
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Drug
Enzyme
Compound
Query: EC:1.10.3.1 (
tyrosinase
)
9,065
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
HPS4
biogenesis of lysosome-related organelles complex 3 subunit 2
(
HPS4
) is one of the genes whose mutations have been associated with Hermansky-Pudlak syndrome (HPS), characterized by ocular albinism and susceptibility to bleeding because of defects in the biogenesis of lysosome-related organelles such as melanosomes.
HPS4
protein forms a BLOC-3 complex with HPS1, another
HPS
gene product, and the complex has been proposed to function as a guanine nucleotide exchange factor (GEF) for RAB32, a member of the Rab small GTPase family (Rab32), and Rab38 (Rab32/38-GEF) and also as a Rab9 effector. Although both Rab32/38 and Rab9 have been shown previously to be involved in melanogenesis in mammalian epidermal melanocytes, the functional relationships of these small GTPases with BLOC-3 remain unknown. In this study, we used site-directed mutagenesis to generate
HPS4
mutants that specifically lack either Rab32/38-GEF activity or Rab9-binding activity and investigated their involvement in melanogenesis of melan-le cells (an
HPS4
-deficient melanocyte cell line derived from
light ear
mice). Melan-le cells exhibit a clear hypopigmentation phenotype,
i.e.
reduced expression and abnormal distribution of
tyrosinase
and reduced melanin content. Although re-expression of WT
HPS4
completely rescued this phenotype, the Rab32/38-GEF activity-deficient
HPS4
mutant failed to restore melanin content and
tyrosinase
trafficking in these cells. Unexpectedly, as WT
HPS4
, the Rab9 binding-deficient
HPS4
mutant completely rescued the phenotype. These results indicate that activation of Rab32/38 by
HPS4
(or BLOC-3) is essential for melanogenesis of cultured melanocytes and that Rab9 likely regulates melanogenesis independently of
HPS4
.
...
PMID:The BLOC-3 subunit HPS4 is required for activation of Rab32/38 GTPases in melanogenesis, but its Rab9 activity is dispensable for melanogenesis. 3083 68