TY - JOUR
T1 - Direct comparison of manganese detoxification/efflux proteins and molecular characterization of ZnT10 protein as a manganese transporter
AU - Nishito, Yukina
AU - Tsuji, Natsuko
AU - Fujishiro, Hitomi
AU - Takeda, Taka Aki
AU - Yamazaki, Tomohiro
AU - Teranishi, Fumie
AU - Okazaki, Fumiko
AU - Matsunaga, Ayu
AU - Tuschl, Karin
AU - Rao, Rajini
AU - Kono, Satoshi
AU - Miyajima, Hiroaki
AU - Narita, Hiroshi
AU - Himeno, Seiichiro
AU - Kambe, Taiho
N1 - Publisher Copyright:
© 2016 by The American Society for Biochemistry and Molecular Biology, Inc.
PY - 2016/7/8
Y1 - 2016/7/8
N2 - Manganese homeostasis involves coordinated regulation of specific proteins involved in manganese influx and efflux. However, the proteins that are involved in detoxification/efflux have not been completely resolved nor has the basis by which they select their metal substrate. Here, we compared six proteins, which were reported to be involved in manganese detoxification/ efflux, by evaluating their ability to reduce manganese toxicity in chicken DT40 cells, finding that human ZnT10 (hZnT10) was the most significant contributor.Adomain swapping and substitution analysis between hZnT10 and the zincspecific transporter hZnT1 showed that residue Asn43, which corresponds to the His residue constituting the potential intramembranous zinc coordination site in other ZnT transporters, is necessary to impart hZnT10's unique manganese mobilization activity; residues Cys52 and Leu242 in transmembrane domains II and V play a subtler role in controlling the metal specificity of hZnT10. Interestingly, the His3Asn reversion mutant in hZnT1 conferred manganese transport activity and loss of zinc transport activity. These results provide important information about manganese detoxification/efflux mechanisms in vertebrate cells as well as the molecular characterization of hZnT10 as a manganese transporter.
AB - Manganese homeostasis involves coordinated regulation of specific proteins involved in manganese influx and efflux. However, the proteins that are involved in detoxification/efflux have not been completely resolved nor has the basis by which they select their metal substrate. Here, we compared six proteins, which were reported to be involved in manganese detoxification/ efflux, by evaluating their ability to reduce manganese toxicity in chicken DT40 cells, finding that human ZnT10 (hZnT10) was the most significant contributor.Adomain swapping and substitution analysis between hZnT10 and the zincspecific transporter hZnT1 showed that residue Asn43, which corresponds to the His residue constituting the potential intramembranous zinc coordination site in other ZnT transporters, is necessary to impart hZnT10's unique manganese mobilization activity; residues Cys52 and Leu242 in transmembrane domains II and V play a subtler role in controlling the metal specificity of hZnT10. Interestingly, the His3Asn reversion mutant in hZnT1 conferred manganese transport activity and loss of zinc transport activity. These results provide important information about manganese detoxification/efflux mechanisms in vertebrate cells as well as the molecular characterization of hZnT10 as a manganese transporter.
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U2 - 10.1074/jbc.M116.728014
DO - 10.1074/jbc.M116.728014
M3 - Article
C2 - 27226609
AN - SCOPUS:84978971402
SN - 0021-9258
VL - 291
SP - 14773
EP - 14787
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 28
ER -