bioimagesUnknownNaoki TamuraThe Journal of Cell Biologyhttps://www.ebi.ac.uk/biostudies/studies/S-JCBD-201302067JCB

PpAtg18-YFP-expressing strain was shifted from synthetic dextrose medium to H₂O.<br /><br />Red: Vacuole stained with FM 4-64, Green: PpAtg18-YFP, Blue: DIC. <br />

Wild-type PpAtg18-YFP-expressing strain was shifted from synthetic methanol medium to synthetic dextrose medium to induce micropexophagy.<br /> Red: Vacuole stained with FM 4-64, Green: PpAtg18-YFP, Blue: DIC. <br />

Wild-type PpAtg18-YFP-expressing strain was grown on synthetic methanol medium prior to induction of pexophagy. Red: Vacuole stained with FM 4-64, Green: PpAtg18-YFP, Blue: DIC. <br /><br />

PpAtg18-YFP-expressing strain was shifted from synthetic dextrose medium to synthetic dextrose medium.<br />Red: Vacuole stained with FM 4-64, Green: PpAtg18-YFP, Blue: DIC. <br />

YFP-tagged PpAtg18 DD mutant was expressed. Cells were shifted from synthetic methanol medium to synthetic dextrose medium to induce micropexophagy. <br />Red: Vacuole stained with FM 4-64, Green: PpAtg18 DD-YFP, Blue: DIC.<br />

PpAtg18-YFP-expressing strain was shifted from synthetic dextrose medium to synthetic dextrose + 0.9 M NaCl medium.<br />Red: Vacuole stained with FM 4-64, Green: PpAtg18-YFP, Blue: DIC. <br />

PpAtg18-YFP-expressing strain was shifted from synthetic dextrose medium to synthetic methanol (YNB + 0.8% methanol) medium.<br />Red: Vacuole stained with FM 4-64, Green: PpAtg18-YFP, Blue: DIC. <br />

PpAtg18-YFP-expressing strain was shifted from synthetic dextrose medium to YNB + 20% glucose medium.<br /><br />Red: Vacuole stained with FM 4-64, Green: PpAtg18-YFP, Blue: DIC.

Wild-type PpAtg18-YFP-expressing strain was shifted from synthetic methanol medium to synthetic ethanol (YNB + 0.8% ethanol) medium to induce macropexophagy.<br /> Red: Vacuole stained with FM 4-64, Green: PpAtg18-YFP, Blue: DIC.

PpAtg18-YFP-expressing fab1∆ strain was shifted from synthetic methanol medium to synthetic dextrose medium to induce micropexophagy.<br />fab1∆<br />

PpAtg18-YFP-expressing strain was shifted from synthetic dextrose (YNB + glucose) medium to YNB medium without glucose.<br />Red: Vacuole stained with FM 4-64, Green: PpAtg18-YFP, Blue: DIC. <br />

YFP-tagged PpAtg18 AA mutant was expressed. Cells were shifted from synthetic methanol medium to synthetic dextrose medium to induce micropexophagy. <br />Red: Vacuole stained with FM 4-64, Green: PpAtg18 AA-YFP, Blue: DIC.<br />

bioimagesImage 291985 (Figure 6 - C)Image 291982 (Figure 4 - B)Image 291987 (Figure 6 - E)Image 291980 (Figure 4 - B)Image 291983 (Figure 6 - C)Image 291978 (Figure 4 - B)Figure 4Figure 4 - BImage 291984 (Figure 6 - C)Figure 6Figure 6 - CImage 291981 (Figure 4 - B)Image 291986 (Figure 6 - C)Image 291988 (Figure 6 - E)Image 291977 (Figure 4 - B)Figure 6 - EImage 291979 (Figure 4 - B)Masahide OkuNaoki TamuraFuyuhiko InagakiYasuyoshi SakaiMoemi ItoNobuo N. NodafalseAtg18 phosphoregulation controls organellar dynamics by modulating its phosphoinositide-binding activity2013-08-12T11:24:45Z2018-11-29T11:24:45Z2018-11-29T11:24:45ZS-JCBD-20130206710.1083/jcb.201302067