ABCD3 p.Leu23Gln

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PMID: 17761678 [PubMed] Kashiwayama Y et al: "Hydrophobic regions adjacent to transmembrane domains 1 and 5 are important for the targeting of the 70-kDa peroxisomal membrane protein."
No. Sentence Comment
88 The lysate was cen- TABLE 2 Oligonucleotide primer sequences used for the generation of mutant PMP70 constructs Conctruct name Forward primer (5؅ 3 3؅) K28A/R29A GCTCTGCCTGCTCCACGCGGCGCGCCGCGCCCTCG R30A/R31A CCTGCTCCACGCGGCGGCCGCCGCCCTCGGCCTGCACG K38A/K39A CCTCGGCCTGCACGGTGCGGCAAGTGGAAAACCACCATTAC P76A/R77A CAGATTCTGAAAATCATGGTCGCTGCAACATTTTGTAAAGAGACAGG K72A GGCTCATACAGATTCTGGCAATCATGGTCGCTGCAAC R66A GGACAAGGTGTTTTTCTCAGCGCTCATACAGATTCTGGC K61A CGAGCTGTGGTGGACGCGGTGTTTTTCTCAGC K53A/K54A/R56A CAATGAGAAAGAGGGGGCAGCAGAGGCAGCTGTGGTGGACGCGG K123A/R124A GGTCGTAGCAGGAAAGATTTCGCGGCATACTTACTCAACTTCATCG R119A/K120A GGTATCATTGGTCGTAGCGCGGCAGATTTCGCGGCATACTTACTC R117A GTGGTATCATTGGTGCTAGCGCGGCAGATTTCGCG L21A/L22A/L23A GTGCCGCGTTCGCTGCTGCTTGCCTGCTCCAC L21Q/L22Q/L23Q GCTGGTGCCGCGTTCCAGCAGCAGTGCCTGCTCCACAAGC I70A/L71A CTCAAGGCTCATACAGGCTGCGAAAATCATGGTCCCTAGAAC I70N/L71Q CTCAAGGCTCATACAGAATCAGAAAATCATGGTCCCTAGAAC I307N/L308Q GGTGGAACACCTACATAATTTCAATCAGTTTCGGTTTTCAATGGGC Peroxisome Targeting Signal of PMP70 NOVEMBER 16, 2007•VOLUME 282•NUMBER 46 JOURNAL OF BIOLOGICAL CHEMISTRY 33833 trifuged at 20,000 ϫ g for 30 min and the His-Pex19p in the supernatant was immediately applied to 10 ml of TALON Metal affinity resin (Clontech) equilibrated with the lysis buffer.
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ABCD3 p.Leu23Gln 17761678:88:772
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129 Under the same condition, PMP70(AA.1-144 L21Q/L22Q/L23Q)- GFP and PMP70(AA.1-144 I70N/L71Q)-GFP were not localized to peroxisomes as negative controls (see Fig. 4).
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ABCD3 p.Leu23Gln 17761678:129:51
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135 To examine whether these hydrophobic motifs are important for the targeting of PMP70, we disrupted these hydrophobic properties by the mutation of L21Q/L22Q/L23Q or I70N/L71Q and examined the subcellular localization.
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ABCD3 p.Leu23Gln 17761678:135:157
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136 When these amino acid residues were substituted for alanines considered to retain the minimum hydrophobic property of these sequences in PMP70(AA.1-144)-GFP, PMP70(AA.1-144 L21A/L22A/L23A)- GFPandPMP70(AA.1-144I70A/L71A)-GFPwerebothlocalized to peroxisomes (Fig. 4A).
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ABCD3 p.Leu23Gln 17761678:136:157
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137 On the other hand, we could not detect the fluorescence of PMP70(AA.1-144 L21Q/L22Q/L23Q)- GFP or PMP70(AA.1-144 I70N/L71Q)-GFP.
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ABCD3 p.Leu23Gln 17761678:137:84
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138 In addition, PMP70(AA.1-144 L21Q/L22Q/L23Q)-GFP and PMP70(AA.1-144 I70N/L71Q)-GFP were not detected by immunoblot analysis under the conditions in which PMP70(AA.1-144)-GFP was detected (Fig. 4B, left).
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ABCD3 p.Leu23Gln 17761678:138:38
status: NEW
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ABCD3 p.Leu23Gln 17761678:138:84
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139 However, in the presence of MG132, a proteasome inhibitor, degradations of these mutant proteins were inhibited, and both PMP70(AA.1-144 L21Q/L22Q/L23Q)-GFP and PMP70(AA.1-144 I70N/L71Q)-GFP exhibited almost the sameexpressionlevelsasthatofPMP70(AA.1-144)-GFP(Fig.4B, right).
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ABCD3 p.Leu23Gln 17761678:139:38
status: NEW
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ABCD3 p.Leu23Gln 17761678:139:147
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140 In this condition, PMP70(AA.1-144)-GFP was still localized to peroxisomes, but PMP70(AA.1-144 L21Q/L22Q/L23Q)- GFP and PMP70(AA.1-144 I70N/L71Q)-GFP did not show any peroxisomal localization (Fig. 4C).
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ABCD3 p.Leu23Gln 17761678:140:104
status: NEW
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ABCD3 p.Leu23Gln 17761678:140:147
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141 Furthermore, full-length PMP70 with the same mutations (PMP70(AA.1-659 L21Q/ Peroxisome Targeting Signal of PMP70 NOVEMBER 16, 2007•VOLUME 282•NUMBER 46 JOURNAL OF BIOLOGICAL CHEMISTRY 33835 PMP70(AA.1-124/TMD4)-GFP PMP70(AA.1-124/TMD6)-GFP PMP70(TMD2)-GFP PMP70(TMD4)-GFP PMP70(TMD6)-GFP PMP70(AA.1-124)-GFP PMP70(AA.1-144)-GFP (B) Peroxisomes GFP Superimposition Peroxisomal localization + - - - - + + 2 113 144 PMP70(TMD2)-GFP 259 4 224 PMP70(TMD4)-GFP 6 314 347 PMP70(TMD6)-GFP 1 259 4 224124 1 1 PMP70(AA.1-124/TMD4)-GFP 124 1 1 6 314 347 PMP70(AA.1-124/TMD6)-GFP 124 1 1 PMP70(AA.1-124)-GFP 1441 1 2PMP70(AA.1-144)-GFP (A) FIGURE 2.
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ABCD3 p.Leu23Gln 17761678:141:104
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145 Peroxisome Targeting Signal of PMP70 33836 L22Q/L23Q)-GFPandPMP70(AA.1-659I70N/L71Q)-GFP)was not localized to peroxisomes either.
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ABCD3 p.Leu23Gln 17761678:145:49
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152 On the other hand, PMP70(AA.1-659 L21Q/L22Q/L23Q) was not well retained in a soluble form, and only 25% of PMP70(AA.1-659 L21Q/ L22Q/L23Q) was recovered in the soluble fraction even in the presence of His-Pex19p.
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ABCD3 p.Leu23Gln 17761678:152:44
status: NEW
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ABCD3 p.Leu23Gln 17761678:152:133
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176 Furthermore, only 15% of the fluorescence of PMP70(AA.224-375)- GFP coincided with that of peroxisomes, which was comparable PMP70(AA.1-144 L21Q/L22Q/L23Q)-GFP PMP70(AA.1-144 I70N/L71Q)-GFP Not detected Not detected PMP70(AA.1-144 I70A/L71A)-GFP PMP70(AA.1-144 L21A/L22A/L23A)-GFP (A) 45.0 31.0 kDa 45.0 31.0 kDa 01enoN µM MG132 (B) PMP70(AA.1-144 L21Q/L22Q/L23Q)-GFP PMP70(AA.1-144 I70N/L71Q)-GFP PMP70(AA.1-659 L21Q/L22Q/L23Q)-GFP PMP70(AA.1-659 I70N/L71Q)-GFP (C) control PMP70(AA.1-144I70N/L71Q)-GFP PMP70(AA.1-144L21Q/L22Q/L23Q)-GFP PMP70(AA.1-144)-GFP control GFP PMP70(AA.1-144I70A/L71A)-GFP PMP70(AA.1-144I70N/L71Q)-GFP PMP70(AA.1-144L21Q/L22Q/L23Q)-GFP PMP70(AA.1-144)-GFP FIGURE 4.
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ABCD3 p.Leu23Gln 17761678:176:150
status: NEW
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ABCD3 p.Leu23Gln 17761678:176:363
status: NEW
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ABCD3 p.Leu23Gln 17761678:176:428
status: NEW
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ABCD3 p.Leu23Gln 17761678:176:533
status: NEW
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ABCD3 p.Leu23Gln 17761678:176:657
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178 A, PMP70(AA.1-144 L21A/L22A/L23A)-GFP, PMP70(AA.1-144 I70A/L71A)-GFP, PMP70(AA.1-144 L21Q/L22Q/L23Q)-GFP, and PMP70(AA.1-144 I70N/L71Q)-GFP were expressed in CHO cells. The subcellular distribution of the fusion proteins was compared with the localization of the endogenous PMP70 detected by immunofluorescence staining with anti-PMP70 COOH-terminal antibody. The peroxisomal staining pattern is shown on the left, EGFP fluorescence in the center, and a superimposition of both stains on the right.
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ABCD3 p.Leu23Gln 17761678:178:95
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181 C, PMP70(AA.1-144 L21Q/L22Q/L23Q)-GFP, PMP70(AA.1-144 I70N/L71Q)-GFP, PMP70(AA.1-659 L21Q/L22Q/L23Q)-GFP, and PMP70(AA.1-659 I70N/L71Q)-GFP were expressed in CHO cells.
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ABCD3 p.Leu23Gln 17761678:181:28
status: NEW
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ABCD3 p.Leu23Gln 17761678:181:95
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182 After incubation with 10 ␮M MG132 for 10 h, the subcellular distribution of PMP70(AA.1-144 L21Q/L22Q/L23Q)-GFP and PMP70(AA.1-144 I70N/L71Q)-GFP wascomparedwiththelocalizationoftheendogenousPMP70detectedbyimmunofluorescencestainingwith anti-PMP70 COOH-terminal antibody, and the subcellular distribution of PMP70(AA.1-659 L21Q/L22Q/L23Q)- GFP and PMP70(AA.1-659 I70N/L71Q)-GFP was compared with the localization of catalase.
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ABCD3 p.Leu23Gln 17761678:182:28
status: NEW
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ABCD3 p.Leu23Gln 17761678:182:95
status: NEW
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ABCD3 p.Leu23Gln 17761678:182:108
status: NEW
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ABCD3 p.Leu23Gln 17761678:182:339
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194 The mutation also affected the targeting of full-length PMP70, so PMP70(AA.1-659 I307N/L308Q)-GFP was not localized to peroxisomes as PMP70(AA.1-659 L21Q/L22Q/L23Q)-GFP and PMP70(AA.1-659 I70N/L71Q)-GFP were not (see Fig. 4C).
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ABCD3 p.Leu23Gln 17761678:194:159
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201 However, PMP70(AA.176-276)-GFP as well as GFP-PMP70(AA.176-276), which corresponded to TMD3-TMD4, did not show any peroxisomal localization, excluding the possibility that only two TMDs and a T S P T S P PMP70 I70N/L71Q - + kDa PMP70 L21Q/L22Q/L23QPMP70 66.2 T S P T S P T S P T S P His-Pex19p - + - + (A) PMP70 L21Q/L22Q/L23Q PMP70 I70N/L71QPMP70 0 20 40 60 soluble% (B) kDa PMP70 L21Q/L22Q/L23Q PMP70 I70N/L71Q 10% input ppt PMP70 10% input ppt 10% input ppt 66.2 (C) 0 20 40 60 80 100 120 relativebound% PMP70 L21Q/L22Q/L23Q PMP70 I70N/L71Q PMP70 (D) FIGURE 5.
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ABCD3 p.Leu23Gln 17761678:201:322
status: NEW
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ABCD3 p.Leu23Gln 17761678:201:392
status: NEW
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ABCD3 p.Leu23Gln 17761678:201:523
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237 On the other hand, both PMP70(AA.1-144 L21Q/L22Q/L23Q)-GFP and PMP70(AA.1-144 I70N/L71Q)- GFP were degraded by proteasomes and did not show any peroxisomal localization even in the presence of proteasome inhibitor (Fig. 4).
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ABCD3 p.Leu23Gln 17761678:237:49
status: NEW
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89 The lysate was cen- TABLE 2 Oligonucleotide primer sequences used for the generation of mutant PMP70 constructs Conctruct name Forward primer (5d15; 3 3d15;) K28A/R29A GCTCTGCCTGCTCCACGCGGCGCGCCGCGCCCTCG R30A/R31A CCTGCTCCACGCGGCGGCCGCCGCCCTCGGCCTGCACG K38A/K39A CCTCGGCCTGCACGGTGCGGCAAGTGGAAAACCACCATTAC P76A/R77A CAGATTCTGAAAATCATGGTCGCTGCAACATTTTGTAAAGAGACAGG K72A GGCTCATACAGATTCTGGCAATCATGGTCGCTGCAAC R66A GGACAAGGTGTTTTTCTCAGCGCTCATACAGATTCTGGC K61A CGAGCTGTGGTGGACGCGGTGTTTTTCTCAGC K53A/K54A/R56A CAATGAGAAAGAGGGGGCAGCAGAGGCAGCTGTGGTGGACGCGG K123A/R124A GGTCGTAGCAGGAAAGATTTCGCGGCATACTTACTCAACTTCATCG R119A/K120A GGTATCATTGGTCGTAGCGCGGCAGATTTCGCGGCATACTTACTC R117A GTGGTATCATTGGTGCTAGCGCGGCAGATTTCGCG L21A/L22A/L23A GTGCCGCGTTCGCTGCTGCTTGCCTGCTCCAC L21Q/L22Q/L23Q GCTGGTGCCGCGTTCCAGCAGCAGTGCCTGCTCCACAAGC I70A/L71A CTCAAGGCTCATACAGGCTGCGAAAATCATGGTCCCTAGAAC I70N/L71Q CTCAAGGCTCATACAGAATCAGAAAATCATGGTCCCTAGAAC I307N/L308Q GGTGGAACACCTACATAATTTCAATCAGTTTCGGTTTTCAATGGGC Peroxisome Targeting Signal of PMP70 NOVEMBER 16, 2007ߦVOLUME 282ߦNUMBER 46 JOURNAL OF BIOLOGICAL CHEMISTRY 33833 trifuged at 20,000 afb; g for 30 min and the His-Pex19p in the supernatant was immediately applied to 10 ml of TALON Metal affinity resin (Clontech) equilibrated with the lysis buffer.
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ABCD3 p.Leu23Gln 17761678:89:772
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130 Under the same condition, PMP70(AA.1-144 L21Q/L22Q/L23Q)- GFP and PMP70(AA.1-144 I70N/L71Q)-GFP were not localized to peroxisomes as negative controls (see Fig. 4).
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ABCD3 p.Leu23Gln 17761678:130:51
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146 Peroxisome Targeting Signal of PMP70 33836 JOURNAL OF BIOLOGICAL CHEMISTRY VOLUME 282ߦNUMBER 46ߦNOVEMBER 16, 2007 at SEMMELWEIS UNIV OF MEDICINE on December 4, L22Q/L23Q)-GFPandPMP70(AA.1-659I70N/L71Q)-GFP)was not localized to peroxisomes either.
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ABCD3 p.Leu23Gln 17761678:146:178
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153 On the other hand, PMP70(AA.1-659 L21Q/L22Q/L23Q) was not well retained in a soluble form, and only 25% of PMP70(AA.1-659 L21Q/ L22Q/L23Q) was recovered in the soluble fraction even in the presence of His-Pex19p.
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ABCD3 p.Leu23Gln 17761678:153:44
status: NEW
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ABCD3 p.Leu23Gln 17761678:153:133
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177 Furthermore, only 15% of the fluorescence of PMP70(AA.224-375)- GFP coincided with that of peroxisomes, which was comparable PMP70(AA.1-144 L21Q/L22Q/L23Q)-GFP PMP70(AA.1-144 I70N/L71Q)-GFP Not detected Not detected PMP70(AA.1-144 I70A/L71A)-GFP PMP70(AA.1-144 L21A/L22A/L23A)-GFP (A) 45.0 31.0 kDa 45.0 31.0 kDa 0 1 e n o N &#b5;M MG132 (B) PMP70(AA.1-144 L21Q/L22Q/L23Q)-GFP PMP70(AA.1-144 I70N/L71Q)-GFP PMP70(AA.1-659 L21Q/L22Q/L23Q)-GFP PMP70(AA.1-659 I70N/L71Q)-GFP (C) control PMP70(AA.1-144 I70N/L71Q)-GFP PMP70(AA.1-144 L21Q/L22Q/L23Q)-GFP PMP70(AA.1-144)-GFP control GFP PMP70(AA.1-144 I70A/L71A)-GFP PMP70(AA.1-144 I70N/L71Q)-GFP PMP70(AA.1-144 L21Q/L22Q/L23Q)-GFP PMP70(AA.1-144)-GFP FIGURE 4.
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ABCD3 p.Leu23Gln 17761678:177:150
status: NEW
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ABCD3 p.Leu23Gln 17761678:177:367
status: NEW
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ABCD3 p.Leu23Gln 17761678:177:432
status: NEW
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ABCD3 p.Leu23Gln 17761678:177:539
status: NEW
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ABCD3 p.Leu23Gln 17761678:177:666
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179 A, PMP70(AA.1-144 L21A/L22A/L23A)-GFP, PMP70(AA.1-144 I70A/L71A)-GFP, PMP70(AA.1-144 L21Q/L22Q/L23Q)-GFP, and PMP70(AA.1-144 I70N/L71Q)-GFP were expressed in CHO cells. The subcellular distribution of the fusion proteins was compared with the localization of the endogenous PMP70 detected by immunofluorescence staining with anti-PMP70 COOH-terminal antibody. The peroxisomal staining pattern is shown on the left, EGFP fluorescence in the center, and a superimposition of both stains on the right.
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ABCD3 p.Leu23Gln 17761678:179:95
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183 After incubation with 10 òe;M MG132 for 10 h, the subcellular distribution of PMP70(AA.1-144 L21Q/L22Q/L23Q)-GFP and PMP70(AA.1-144 I70N/L71Q)-GFP wascomparedwiththelocalizationoftheendogenousPMP70detectedbyimmunofluorescencestainingwith anti-PMP70 COOH-terminal antibody, and the subcellular distribution of PMP70(AA.1-659 L21Q/L22Q/L23Q)- GFP and PMP70(AA.1-659 I70N/L71Q)-GFP was compared with the localization of catalase.
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ABCD3 p.Leu23Gln 17761678:183:107
status: NEW
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ABCD3 p.Leu23Gln 17761678:183:338
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195 The mutation also affected the targeting of full-length PMP70, so PMP70(AA.1-659 I307N/L308Q)-GFP was not localized to peroxisomes as PMP70(AA.1-659 L21Q/L22Q/L23Q)-GFP and PMP70(AA.1-659 I70N/L71Q)-GFP were not (see Fig. 4C).
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ABCD3 p.Leu23Gln 17761678:195:159
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202 However, PMP70(AA.176-276)-GFP as well as GFP-PMP70(AA.176-276), which corresponded to TMD3-TMD4, did not show any peroxisomal localization, excluding the possibility that only two TMDs and a T S P T S P PMP70 I70N/L71Q - + kDa PMP70 L21Q/L22Q/L23Q PMP70 66.2 T S P T S P T S P T S P His-Pex19p - + - + (A) PMP70 L21Q/L22Q/L23Q PMP70 I70N/L71Q PMP70 0 20 40 60 soluble % (B) kDa PMP70 L21Q/L22Q/L23Q PMP70 I70N/L71Q 10% input ppt PMP70 10% input ppt 10% input ppt 66.2 (C) 0 20 40 60 80 100 120 relative bound % PMP70 L21Q/L22Q/L23Q PMP70 I70N/L71Q PMP70 (D) FIGURE 5.
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ABCD3 p.Leu23Gln 17761678:202:244
status: NEW
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ABCD3 p.Leu23Gln 17761678:202:323
status: NEW
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ABCD3 p.Leu23Gln 17761678:202:395
status: NEW
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ABCD3 p.Leu23Gln 17761678:202:528
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238 On the other hand, both PMP70(AA.1-144 L21Q/L22Q/L23Q)-GFP and PMP70(AA.1-144 I70N/L71Q)- GFP were degraded by proteasomes and did not show any peroxisomal localization even in the presence of proteasome inhibitor (Fig. 4).
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ABCD3 p.Leu23Gln 17761678:238:49
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