Abstract:Vacuoles of several types can be observed in pollen throughout its development. Their physiological significance reflects the complexity of the biological process leading to functional pollen grains. Vacuolisation always occurs during pollen development but when ripe pollen is shed the extensive translucent vacuoles present in the vegetative parts in previous stages are absent. Vacuole functions vary according to developmental stage but in ripe pollen they are mainly storage sites for reserves. Vacuoles cause … Show more
“…Until stage 10, the ap2m-1 mutant plants did not display any noticeable difference to the wild type (see Supplemental Figure 8 online). However, the most prominent difference was detected at stage 13 when the central vacuole (CV) undergoes degeneration (Yamamoto et al, 2003;Pacini et al, 2011). In wild-type pollen grains, the CV was fragmented into numerous small vacuoles <0.3 mm in diameter and uniformly distributed in the entire cellular space.…”
Section: Ap2m-1 Mutants Have Multiple Defects In Processes Involved Imentioning
“…Until stage 10, the ap2m-1 mutant plants did not display any noticeable difference to the wild type (see Supplemental Figure 8 online). However, the most prominent difference was detected at stage 13 when the central vacuole (CV) undergoes degeneration (Yamamoto et al, 2003;Pacini et al, 2011). In wild-type pollen grains, the CV was fragmented into numerous small vacuoles <0.3 mm in diameter and uniformly distributed in the entire cellular space.…”
Section: Ap2m-1 Mutants Have Multiple Defects In Processes Involved Imentioning
“…Plant vacuoles are versatile organelles critical for plant growth and responses to the environment (Pacini et al, 2011). The functionality of vacuoles is fulfilled through proteins localized at the vacuolar membrane (i.e.…”
ORCID IDs: 0000-0001-6345-6855 (J.-G.W.); 0000-0002-3501-5857 (Y.Z.).Plant vacuoles are versatile organelles critical for plant growth and responses to environment. Vacuolar proteins are transported from the endoplasmic reticulum via multiple routes in plants. Two classic routes bear great similarity to other phyla with major regulators known, such as COPII and Rab5 GTPases. By contrast, vacuolar trafficking mediated by adaptor protein-3 (AP-3) or that independent of the Golgi has few recognized cargos and none of the regulators. In search of novel regulators for vacuolar trafficking routes and by using a fluorescence-based forward genetic screen, we demonstrated that the multispan transmembrane protein, Arabidopsis (Arabidopsis thaliana) PROTEIN S-ACYL TRANSFERASE10 (PAT10), is an AP-3-mediated vacuolar cargo. We show that the tonoplast targeting of PAT10 is mediated by the AP-3 complex but independent of the Rab5-mediated post-Golgi trafficking route. We also report that AP-3-mediated vacuolar trafficking involves a subpopulation of COPII and requires the vacuolar tethering complex HOPS. In addition, we have identified two novel mutant alleles of AP-3d, whose point mutations interfered with the formation of the AP-3 complex as well as its membrane targeting. The results presented here shed new light on the vacuolar trafficking route mediated by AP-3 in plant cells.
“…In angiosperms, water and nutrient status regulation is relevant for pollen development, germination, and pollen tube growth (Samuel et al, 2009;Pacini et al, 2011;Firon et al, 2012). During its developmental program and functioning, pollen grains experience changes in water and nutrient content in relation to the surrounding environment (reviewed in Firon et al, 2012).…”
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