PMID: 16098482

Noguchi T, Ren XQ, Aoki S, Igarashi Y, Che XF, Nakajima Y, Takahashi H, Mitsuo R, Tsujikawa K, Sumizawa T, Haraguchi M, Kobayashi M, Goto S, Kanehisa M, Aikou T, Akiyama S, Furukawa T
MRP1 mutated in the L0 region transports SN-38 but not leukotriene C4 or estradiol-17 (beta-D-glucuronate).
Biochem Pharmacol. 2005 Oct 1;70(7):1056-65., 2005-10-01 [PubMed]
Sentences
No. Mutations Sentence Comment
4 ABCC1 p.Trp222Leu
X
ABCC1 p.Trp222Leu 16098482:4:47
status: NEW
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ABCC1 p.Trp223Leu
X
ABCC1 p.Trp223Leu 16098482:4:54
status: NEW
view ABCC1 p.Trp223Leu details
ABCC1 p.Arg230Ala
X
ABCC1 p.Arg230Ala 16098482:4:64
status: NEW
view ABCC1 p.Arg230Ala details
In this paper, we further tested the effect of W222L, W223L and R230A mutations in MRP1, designated dmL0MRP1, on MRP1 transport activity. Login to comment
60 ABCC1 p.Trp261Ala
X
ABCC1 p.Trp261Ala 16098482:60:140
status: NEW
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ABCC1 p.Lys267Met
X
ABCC1 p.Lys267Met 16098482:60:150
status: NEW
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In order to completely disrupt LTC4 transport activity, we created additional mutations in the L0 region of MRP1 that already expressed the W261A and K267M mutations. Login to comment
61 ABCC1 p.Trp222Leu
X
ABCC1 p.Trp222Leu 16098482:61:29
status: NEW
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ABCC1 p.Trp223Leu
X
ABCC1 p.Trp223Leu 16098482:61:36
status: NEW
view ABCC1 p.Trp223Leu details
ABCC1 p.Arg230Ala
X
ABCC1 p.Arg230Ala 16098482:61:46
status: NEW
view ABCC1 p.Arg230Ala details
The extra mutations created, W222L, W223L and R230A, were located within WxxxxxK sequences in the L0 region that have been reported to an interacting site of glutathione-S-transferase with GSH. Login to comment
63 ABCC1 p.Trp261Ala
X
ABCC1 p.Trp261Ala 16098482:63:17
status: NEW
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ABCC1 p.Lys267Met
X
ABCC1 p.Lys267Met 16098482:63:27
status: NEW
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Practically, the W261A and K267M mutations were first introduced into wt MRP1 by PCR using primers described in a previous paper [15]. Login to comment
64 ABCC1 p.Trp222Leu
X
ABCC1 p.Trp222Leu 16098482:64:0
status: NEW
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ABCC1 p.Trp223Leu
X
ABCC1 p.Trp223Leu 16098482:64:7
status: NEW
view ABCC1 p.Trp223Leu details
ABCC1 p.Arg230Ala
X
ABCC1 p.Arg230Ala 16098482:64:17
status: NEW
view ABCC1 p.Arg230Ala details
W222L, W223L and R230A mutations were then introduced into this construct by PCR using the forward primers, 50 -GGGTTGATTGTCGCGGGCTACCGCC-30 , and reverse primer 50 -TGTGATCAACAAGAAGGTGATCC- TC-30 (bold denotes mismatched bases encoding the mutation). Login to comment
136 ABCC1 p.Trp261Ala
X
ABCC1 p.Trp261Ala 16098482:136:168
status: NEW
view ABCC1 p.Trp261Ala details
ABCC1 p.Lys267Met
X
ABCC1 p.Lys267Met 16098482:136:178
status: NEW
view ABCC1 p.Lys267Met details
ABCC1 p.Trp222Leu
X
ABCC1 p.Trp222Leu 16098482:136:107
status: NEW
view ABCC1 p.Trp222Leu details
ABCC1 p.Trp223Leu
X
ABCC1 p.Trp223Leu 16098482:136:114
status: NEW
view ABCC1 p.Trp223Leu details
ABCC1 p.Arg230Ala
X
ABCC1 p.Arg230Ala 16098482:136:124
status: NEW
view ABCC1 p.Arg230Ala details
As described in Section 2, the new mutant MRP1, named dmL0MRP1, was designed to carry the extra mutations, W222L, W223L and R230A, in addition to the previous mutants, W261A and K267M, in L0 region, and the original TMD0 region, in order to avoid the influence of deletion of the TMD0 region (Fig. 1). Login to comment