학술논문

Effects of individual amino acid mutations of zinc transporter ZIP8 on manganese- and cadmium-transporting activity.
Document Type
Article
Source
Biochemical & Biophysical Research Communications. Aug2022, Vol. 616, p26-32. 7p.
Subject
*ZINC transporters
*AMINO acid residues
*AMINO acids
*GENOME-wide association studies
*GENETIC mutation
*CADMIUM
Language
ISSN
0006-291X
Abstract
Zinc (Zn) transporter ZIP8, encoded by SLC39A8 , is a unique transporter that can transport divalent manganese (Mn) and cadmium (Cd) in addition to Zn. Recently, associations between various human diseases and variant forms of ZIP8 have been reported. Four amino acid residues, V33, G38, S335, and I340, of human ZIP8 (hZIP8) are mutated in patients with congenital disorders of glycosylation (CDG), whose blood Mn levels are extremely low. Many genome-wide association studies have reported that the A391T mutation of hZIP8 caused by rs13107325 is associated with a wide range of diseases. However, the roles of individual mutations of hZIP8 on metal-transporting activity remain elusive. We established DT40 cells respectively expressing the four mutant hZIP8s and compared the Mn- and Cd-transporting activity between the mutants and wild-type hZIP8. Among the four mutations observed in the ZIP8-mutated CDG patients, the S335T and I340 N mutations in the predicted transmembrane domain 5 (TMD5) completely abolished Mn- and Cd-transporting activity, while V33 M or G35R mutations at the N-terminus did not. We also examined the A391T mutation, which slightly reduced metal transporting activity. Finally, we examined the effects of artificial mutations in the metal-binding motif EEXXH in the TMD5. Replacing EEXXH with HEXXH, which exists in most ZIP transporters, abolished the Mn- and Cd-transporting activity of hZIP8, indicating that glutamic acid in this motif plays a critical role in the unique affinity of ZIP8 for Mn and Cd. Thus, the utilization of DT40 cells enabled us to clarify the different functions of each residue of hZIP8 on metal transport. [Display omitted] • Multiple mutations of Zn transporter ZIP8 are involved in Mn metabolism disorders. • We established DT40 cells stably expressing wild-type or mutant human ZIP8. • Mutations of residues in TMD5 resulted in the loss of Mn/Cd-transporting activity. • Mutations of residues in the N-terminus did not affect metal permeation capacity. • Replacing EEXXH motif in TMD5 with HEXXH abolished Mn/Cd transport capacity of ZIP8. [ABSTRACT FROM AUTHOR]