Defects in peroxisomal 6-phosphogluconate dehydrogenase isoform PGD2 prevent gametophytic interaction in Arabidopsis thaliana [Defekte in der peroxisomalen 6-Phosphogluconat-Dehydrogenase Isoform PGD2 verhindern die gametophytische Interaktion in Arabidopsis thaliana]Open Access

Hölscher, C; Lutterbey, MC; Lansing, H; Meyer, T; Fischer, K; von Schaewen, A

Research article (journal) | Peer reviewed

Abstract

We studied localization of the 6-phosphogluconate dehydrogenase (PGD) isoforms of Arabidopsis thaliana. Similar polypeptide lengths of PGD1, PGD2, and PGD3 obscured which isoform may represent the cytosolic and/or plastidic enzyme, plus whether PGD2 with peroxisomal targeting motif (PTS1) might also target plastids. Reporter-fusion analyses in protoplasts revealed that with free N-terminus, PGD1 and PGD3 accumulate in the cytosol and chloroplasts, whereas PGD2 remains in the cytosol. Mutagenesis of a conserved second ATG enhanced plastidic localization of PGD1 and PGD3 but not PGD2. N-terminal deletions in PGD2 fusions with free C-termini resulted in peroxisomal import upon dimerization; plus PGD2 could be immuno-detected in purified peroxisomes. Repeated selfing of pgd2 T-DNA alleles yielded no homozygous mutants, although siliques and seeds of heterozygous plants developed normally. Detailed analyses of the C-terminally truncated PGD2-1 protein showed that peroxisomal import and catalytic activity are abolished. Reciprocal backcrosses of pgd2-1 suggested that missing 6PGDH activity in peroxisomes affects the male gametophyte. Tetrad analyses in the qrt1-2 background revealed that pgd2-1 pollen is vital and in-vitro germination normal, but pollen-tube growth inside stylar tissues apparently less directed. Mutual gametophytic sterility was overcome by complementation with a genomic construct, but not with a version lacking the first ATG. These analyses showed that peroxisomal PGD2 activity is required for guided growth of the male gametophytes and pollen tube-ovule interaction. Our report finally demonstrates an essential role for OPPP reactions in peroxisomes, possibly to maintain critical levels of nitric oxide and/or jasmonic acid, whose biosyntheses both depend on NADPH provision.

Details about the publication

JournalPlant Physiology (Plant Phys)
Volume171
Issue1
Page range192-205
StatusPublished
Release year2016 (03/03/2016)
Language in which the publication is writtenEnglish
KeywordsOxidative Pentose-Phosphate pathway; 6-Phosphogluconate dehydrogenase isoforms; Arabidopsis; peroxisome versus cytosol/plastid targeting

Authors from the University of Münster

Hölscher, Christian
Lansing, Hannes
Lutterbey, Marie Christin
Meyer, Tanja
von Schaewen, Antje

Doctorates the publication originates from

Die Rolle der dualen Zielsteuerung plastidär/peroxisomaler Enzyme des Oxidativen Penstosephosphatweges in Arabidopsis thaliana
Candidate: Hölscher, Christian | Supervisors: von Schaewen, Antje; Weis, Engelbert; Hippler Michael
Period of time: until 30/06/2014
Doctoral examination procedure finished at: Doctoral examination procedure at University of Münster