TY - JOUR
T1 - Missense mutations that inactivate the Aspergillus nidulans nrtA gene encoding a high-affinity nitrate transporter
AU - Kinghorn, James Robertson
AU - Sloan, J
AU - Kana'n, GJM
AU - DaSilva, ER
AU - Rouch, DA
AU - Unkles, Sheila Eileen
PY - 2005/3
Y1 - 2005/3
N2 - The transport of nitrate into prokaryotic and eukaryotic cells, of considerable interest to agriculture, ecology, and human health, is carried out by members of a distinct cluster of proteins within the major facilitator superfamily. To obtain structure/function information on this important class of nitrate permeases, a collection of chemically induced mutations in the nrtA gene encoding a 12-transmembrane domain, high-affinity nitrate transporter from the eukaryote Aspergillus nidulans was isolated and characterized. This mutational analysis, coupled with protein alignments, demonstrates the utility of the approach to predicting peptide motifs and individual residues important for the movement of nitrate across the membrane. These include the highly conserved nitrate signature motif (residues 166-173) in Tm 5, the conserved charged residues Arg87 (Tm 2) and Arg368 (Tm 8), as well as the aromatic residue Phc47 (Tm 1), all within transmembrane helices. No mutations were observed in the large central loop (Lp 6/7) between Tm 6 and Tm 7. Finally, the study of a strain with a conversion of Trp481 (Tm 12) to a stop codon suggests that all 12 transmembrane domains and/or the C-terminal tail are required for membrane insertion and/or stability of NrtA.
AB - The transport of nitrate into prokaryotic and eukaryotic cells, of considerable interest to agriculture, ecology, and human health, is carried out by members of a distinct cluster of proteins within the major facilitator superfamily. To obtain structure/function information on this important class of nitrate permeases, a collection of chemically induced mutations in the nrtA gene encoding a 12-transmembrane domain, high-affinity nitrate transporter from the eukaryote Aspergillus nidulans was isolated and characterized. This mutational analysis, coupled with protein alignments, demonstrates the utility of the approach to predicting peptide motifs and individual residues important for the movement of nitrate across the membrane. These include the highly conserved nitrate signature motif (residues 166-173) in Tm 5, the conserved charged residues Arg87 (Tm 2) and Arg368 (Tm 8), as well as the aromatic residue Phc47 (Tm 1), all within transmembrane helices. No mutations were observed in the large central loop (Lp 6/7) between Tm 6 and Tm 7. Finally, the study of a strain with a conversion of Trp481 (Tm 12) to a stop codon suggests that all 12 transmembrane domains and/or the C-terminal tail are required for membrane insertion and/or stability of NrtA.
KW - MAJOR FACILITATOR SUPERFAMILY
KW - BACTERIAL OXALATE TRANSPORTER
KW - ESCHERICHIA-COLI
KW - LACTOSE PERMEASE
KW - CHLORATE TOXICITY
KW - MEMBRANE-PROTEINS
KW - CONSERVED MOTIF
KW - ASSIMILATION
KW - MECHANISM
KW - BIOSYNTHESIS
UR - http://www.scopus.com/inward/record.url?scp=17444412593&partnerID=8YFLogxK
UR - http://www.genetics.org/cgi/reprint/169/3/1369?maxtoshow=&HITS=10&hits=10&RESULTFORMAT=&author1=unkles&searchid=1&FIRSTINDEX=0&resourcetype=HWCIT
U2 - 10.1534/genetics.104.036590
DO - 10.1534/genetics.104.036590
M3 - Article
SN - 0016-6731
VL - 169
SP - 1369
EP - 1377
JO - Genetics
JF - Genetics
IS - 3
ER -