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Main Authors: Jiang, Kunyin, Yu, Hong, Kong, Lingfeng, Liu, Shikai, Du, Shaojun, Li, Qi
Format: Artículo científico
Language:en
Published: Marine biotechnology (New York, N.Y.) 2025
Subjects:
Online Access:https://pubmed.ncbi.nlm.nih.gov/40035897/
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author Jiang, Kunyin
Yu, Hong
Kong, Lingfeng
Liu, Shikai
Du, Shaojun
Li, Qi
author_facet Jiang, Kunyin
Yu, Hong
Kong, Lingfeng
Liu, Shikai
Du, Shaojun
Li, Qi
Jiang, Kunyin
Yu, Hong
Kong, Lingfeng
Liu, Shikai
Du, Shaojun
Li, Qi
collection PubMed - marine biology
contents DOPA Decarboxylase (DDC) in Pacific Oysters: Characterization and Role in Tyrosine Metabolism and Melanogenesis. Jiang, Kunyin Yu, Hong Kong, Lingfeng Liu, Shikai Du, Shaojun Li, Qi Animals Dopa Decarboxylase Melanins Crassostrea Tyrosine Levodopa Dopamine Cyclic AMP Phylogeny Amino Acid Sequence Melanogenesis DOPA decarboxylase (DDC) plays a crucial role in the physiological functions of animals by participating in the dopaminergic system. However, the functions of DDC in shellfish remain poorly understood. The Pacific oyster (Crassostrea gigas) is an extensively cultivated shellfish. In this study, we characterized a DDC gene, designated CgDDC, from C. gigas. The CgDDC gene encodes a protein that contains a Pyridoxal_deC domain, which features specific binding sites for pyridoxal-5'-phosphate (PLP) and L-DOPA. CgDDC exhibits a significantly higher expression level in the black shell oyster strain than the white strain. In vitro enzymatic reaction assays demonstrated that CgDDC catalyzes the conversion of L-DOPA to dopamine. In vivo experiments revealed that inhibiting CgDDC activity reduced the expression of genes associated with tyrosine metabolism. Furthermore, the knockdown of CgDDC caused a decline in cAMP level and reduced transcription of genes involved in the cAMP-mediated melanogenesis. Additionally, treatment with L-α-DOPA inhibited CgDDC enzyme activity and cAMP-mediated melanogenesis; however, dopamine supplementation countered this inhibition, maintaining gene expression and melanin content at baseline levels. Collectively, our findings suggest that CgDDC is intricately involved in regulating tyrosine metabolism and melanogenesis in C. gigas.
format Artículo científico
id pubmed_40035897
institution PubMed
language en
publishDate 2025
publisher Marine biotechnology (New York, N.Y.)
record_format pubmed
spellingShingle DOPA Decarboxylase (DDC) in Pacific Oysters: Characterization and Role in Tyrosine Metabolism and Melanogenesis.
Jiang, Kunyin
Yu, Hong
Kong, Lingfeng
Liu, Shikai
Du, Shaojun
Li, Qi
Animals
Dopa Decarboxylase
Melanins
Crassostrea
Tyrosine
Levodopa
Dopamine
Cyclic AMP
Phylogeny
Amino Acid Sequence
Melanogenesis
DOPA Decarboxylase (DDC) in Pacific Oysters: Characterization and Role in Tyrosine Metabolism and Melanogenesis. Jiang, Kunyin Yu, Hong Kong, Lingfeng Liu, Shikai Du, Shaojun Li, Qi Animals Dopa Decarboxylase Melanins Crassostrea Tyrosine Levodopa Dopamine Cyclic AMP Phylogeny Amino Acid Sequence Melanogenesis DOPA decarboxylase (DDC) plays a crucial role in the physiological functions of animals by participating in the dopaminergic system. However, the functions of DDC in shellfish remain poorly understood. The Pacific oyster (Crassostrea gigas) is an extensively cultivated shellfish. In this study, we characterized a DDC gene, designated CgDDC, from C. gigas. The CgDDC gene encodes a protein that contains a Pyridoxal_deC domain, which features specific binding sites for pyridoxal-5'-phosphate (PLP) and L-DOPA. CgDDC exhibits a significantly higher expression level in the black shell oyster strain than the white strain. In vitro enzymatic reaction assays demonstrated that CgDDC catalyzes the conversion of L-DOPA to dopamine. In vivo experiments revealed that inhibiting CgDDC activity reduced the expression of genes associated with tyrosine metabolism. Furthermore, the knockdown of CgDDC caused a decline in cAMP level and reduced transcription of genes involved in the cAMP-mediated melanogenesis. Additionally, treatment with L-α-DOPA inhibited CgDDC enzyme activity and cAMP-mediated melanogenesis; however, dopamine supplementation countered this inhibition, maintaining gene expression and melanin content at baseline levels. Collectively, our findings suggest that CgDDC is intricately involved in regulating tyrosine metabolism and melanogenesis in C. gigas.
title DOPA Decarboxylase (DDC) in Pacific Oysters: Characterization and Role in Tyrosine Metabolism and Melanogenesis.
topic Animals
Dopa Decarboxylase
Melanins
Crassostrea
Tyrosine
Levodopa
Dopamine
Cyclic AMP
Phylogeny
Amino Acid Sequence
Melanogenesis
url https://pubmed.ncbi.nlm.nih.gov/40035897/