ABCD3 p.Leu308Gln
[switch to full view]Comments [show]
None has been submitted yet.
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.
X
ABCD3 p.Leu308Gln 17761678:88:930
status: NEW191 GFP-PMP70(AA.263-375 I307N/L308Q) was detected only in the presence of MG132.
X
ABCD3 p.Leu308Gln 17761678:191:27
status: NEW193 However, under the same conditions, GFP-PMP70(AA.263-375 I307N/L308Q) did not show any peroxisomal localization (Fig. 8).
X
ABCD3 p.Leu308Gln 17761678:193:63
status: NEW194 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).
X
ABCD3 p.Leu308Gln 17761678:194:63
status: NEWX
ABCD3 p.Leu308Gln 17761678:194:87
status: NEW196 To characterize the hydrophobic motif in the targeting process of PMP70 more precisely, we examined the interaction between PMP70(AA.1-659 I307N/L308Q) and Pex19p.
X
ABCD3 p.Leu308Gln 17761678:196:145
status: NEW197 As shown in Fig. 9, PMP70(AA.1-659 I307N/L308Q) translated in the wheat germ in vitro translation system was almost recovered as a soluble protein in the presence of purified His-Pex19p, and PMP70(AA.1-659 I307N/L308Q) interacted with Pex19p at almost the same efficiency as PMP70(AA.1-659).
X
ABCD3 p.Leu308Gln 17761678:197:41
status: NEWX
ABCD3 p.Leu308Gln 17761678:197:145
status: NEWX
ABCD3 p.Leu308Gln 17761678:197:212
status: NEW243 Peroxisome Targeting Signal of PMP70 NOVEMBER 16, 2007•VOLUME 282•NUMBER 46 JOURNAL OF BIOLOGICAL CHEMISTRY 33841 acid pair existing just adjacent to TMD5 was important for the targeting to peroxisomes; GFP-PMP70(AA.263-375 I307A/L308A) was directed to peroxisomes, but GFP-PMP70(AA.263-375 I307N/L308Q) was not (Fig. 8).
X
ABCD3 p.Leu308Gln 17761678:243:312
status: NEW257 GFP-PMP70(AA.263-375 I307N/L308Q) PMP70(AA.1-659 I307N/L308Q)-GFP GFP-PMP70(AA.263-375) FIGURE 8.
X
ABCD3 p.Leu308Gln 17761678:257:27
status: NEWX
ABCD3 p.Leu308Gln 17761678:257:55
status: NEW259 GFP-PMP70(AA.264-375 I307N/L308Q) and PMP70(AA.1-659 I307N/L308Q)-GFP, which are disrupted in the hydrophobic property adjacent to the NH2-terminal side of TMD5, were expressed in CHO cells.
X
ABCD3 p.Leu308Gln 17761678:259:27
status: NEWX
ABCD3 p.Leu308Gln 17761678:259:59
status: NEW260 After incubation with 10 ␮M MG132 for 10 h, the subcellular distribution of GFP-PMP70(AA.264-375 I307N/L308Q) was compared with the localization of the endogenous PMP70 detected by immunofluorescence staining with anti-PMP70 COOH-terminal antibody,andthesubcellulardistributionofPMP70(AA.1-659I307N/L308Q)- GFP was compared with the localization of catalase.
X
ABCD3 p.Leu308Gln 17761678:260:27
status: NEWX
ABCD3 p.Leu308Gln 17761678:260:59
status: NEWX
ABCD3 p.Leu308Gln 17761678:260:110
status: NEWX
ABCD3 p.Leu308Gln 17761678:260:306
status: NEW262 (B) (A) 0 20 40 60 80 100 120 relativebound% PMP70 I307N/L308Q PMP70 kDa PMP70 I307N/L308Q 10% input ppt PMP70 10% input ppt 66.2 FIGURE 9.
X
ABCD3 p.Leu308Gln 17761678:262:57
status: NEWX
ABCD3 p.Leu308Gln 17761678:262:85
status: NEW264 A, PMP70 and PMP70(I307N/L308Q) were translated and labeled with [35 S]methionine invitrointhepresenceofHis-Pex19p.Aftercentrifugationat17,000ϫgfor20 min at 4 °C, soluble proteins were subjected to immunoprecipitation using anti-His G antibody. Co-purified proteins were analyzed by SDS-PAGE followed by autoradiography. The arrowhead indicates the position of PMP70 and the mutant.
X
ABCD3 p.Leu308Gln 17761678:264:25
status: NEW278 However, we also found that PMP70(AA.1-659 I70N/L71Q) and PMP70(AA.1-659 I307N/L308Q) lost the targeting activity, although these mutant proteins still interacted with Pex19p and were solubilized by Pex19p, suggesting that the targeting element and Pex19p-binding site of PMP70 are functionally separated.
X
ABCD3 p.Leu308Gln 17761678:278:79
status: NEW89 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.
X
ABCD3 p.Leu308Gln 17761678:89:930
status: NEW192 GFP-PMP70(AA.263-375 I307N/L308Q) was detected only in the presence of MG132.
X
ABCD3 p.Leu308Gln 17761678:192:27
status: NEW195 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).
X
ABCD3 p.Leu308Gln 17761678:195:87
status: NEW198 As shown in Fig. 9, PMP70(AA.1-659 I307N/L308Q) translated in the wheat germ in vitro translation system was almost recovered as a soluble protein in the presence of purified His-Pex19p, and PMP70(AA.1-659 I307N/L308Q) interacted with Pex19p at almost the same efficiency as PMP70(AA.1-659).
X
ABCD3 p.Leu308Gln 17761678:198:41
status: NEWX
ABCD3 p.Leu308Gln 17761678:198:212
status: NEW244 Peroxisome Targeting Signal of PMP70 NOVEMBER 16, 2007ߦVOLUME 282ߦNUMBER 46 JOURNAL OF BIOLOGICAL CHEMISTRY 33841 acid pair existing just adjacent to TMD5 was important for the targeting to peroxisomes; GFP-PMP70(AA.263-375 I307A/L308A) was directed to peroxisomes, but GFP-PMP70(AA.263-375 I307N/L308Q) was not (Fig. 8).
X
ABCD3 p.Leu308Gln 17761678:244:310
status: NEW258 GFP-PMP70(AA.263-375 I307N/L308Q) PMP70(AA.1-659 I307N/L308Q)-GFP GFP-PMP70(AA.263-375) FIGURE 8.
X
ABCD3 p.Leu308Gln 17761678:258:27
status: NEWX
ABCD3 p.Leu308Gln 17761678:258:55
status: NEW261 After incubation with 10 òe;M MG132 for 10 h, the subcellular distribution of GFP-PMP70(AA.264-375 I307N/L308Q) was compared with the localization of the endogenous PMP70 detected by immunofluorescence staining with anti-PMP70 COOH-terminal antibody,andthesubcellulardistributionofPMP70(AA.1-659I307N/L308Q)- GFP was compared with the localization of catalase.
X
ABCD3 p.Leu308Gln 17761678:261:109
status: NEWX
ABCD3 p.Leu308Gln 17761678:261:305
status: NEW263 (B) (A) 0 20 40 60 80 100 120 relative bound % PMP70 I307N/L308Q PMP70 kDa PMP70 I307N/L308Q 10% input ppt PMP70 10% input ppt 66.2 FIGURE 9.
X
ABCD3 p.Leu308Gln 17761678:263:59
status: NEWX
ABCD3 p.Leu308Gln 17761678:263:87
status: NEW265 A, PMP70 and PMP70(I307N/L308Q) were translated and labeled with [35 S]methionine invitrointhepresenceofHis-Pex19p.Aftercentrifugationat17,000afb;gfor20 min at 4 &#b0;C, soluble proteins were subjected to immunoprecipitation using anti-His G antibody. Co-purified proteins were analyzed by SDS-PAGE followed by autoradiography. The arrowhead indicates the position of PMP70 and the mutant.
X
ABCD3 p.Leu308Gln 17761678:265:25
status: NEW279 However, we also found that PMP70(AA.1-659 I70N/L71Q) and PMP70(AA.1-659 I307N/L308Q) lost the targeting activity, although these mutant proteins still interacted with Pex19p and were solubilized by Pex19p, suggesting that the targeting element and Pex19p-binding site of PMP70 are functionally separated.
X
ABCD3 p.Leu308Gln 17761678:279:79
status: NEW