Abstract

Late 19th-century cytologists observed tiny oil drops in shoot parenchyma and seeds, but it was discovered only in 1972 that they were bound by a half unit-membrane. Later, it was found that lipid bodies (LBs) arise from the endoplasmic reticulum. Seeds are known to be packed with static LBs, coated with the LB-specific protein OLEOSIN. As shown here, apices of Populus tremula x P. tremuloides also express OLEOSIN genes and produce potentially mobile LBs. In developing buds, PtOLEOSIN (PtOLE) genes were upregulated, especially PtOLE6, concomitant with LB accumulation. To investigate LB mobility and destinations, we transformed Arabidopsis with PtOLE6-eGFP. We found that PtOLE6-eGFP fusion protein co-localized with Nile Red-stained LBs in all cell types. Moreover, PtOLE6-eGFP-tagged LBs targeted plasmodesmata, identified by the callose marker aniline blue. Pharmacological experiments with brefeldin, cytochalasin D, and oryzalin showed that LB-trafficking requires F-actin, implying involvement of myosin motors. In a triple myosin-XI knockout (xi-k/1/2), transformed with PtOLE6-eGFP, trafficking of PtOLE6-eGFP-tagged LBs was severely impaired, confirming that they move on F-actin, motorized by myosin XIs. The data reveal that LBs and OLEOSINs both function in proliferating apices and buds, and that directional trafficking of LBs to plasmodesmata requires the actomyosin system.

Highlights

  • The presence of cytosolic lipid inclusions was first noticed in the late 19th century in parenchyma cells of roots and shoot-axils, and seeds of Ricinus [1]. It is well-established that cytosolic “oil drops,” as described by the early plant cytologists, are of universal occurrence [2,3,4]. Their origin, structure, and precise composition remained elusive for many decades, which is reflected in the plethora of descriptive names that sprang up, including lipid droplets, fat droplets, oil droplets, oil globules, oleosomes, spherosomes, oil bodies, and lipid bodies [2,5]

  • The shoot apex produces nascent axillary buds (AXBs) in the axils of emerging leaves, which gradually develop toward completion (Figure 1b)

  • The shoot apical meristem (SAM) produces a terminal bud (TB; Figure 1c) that adopts the developmental program of AXBs [68] and establishes a dormant state [52,69]

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Summary

Introduction

The presence of cytosolic lipid inclusions was first noticed in the late 19th century in parenchyma cells of roots and shoot-axils, and seeds of Ricinus [1]. It is well-established that cytosolic “oil drops,” as described by the early plant cytologists, are of universal occurrence [2,3,4]. It was suggested that spherosomes may result from the local deposition of oil between the leaflets of unit-membranes, a hypothesis that was supported by the presence of structural membrane proteins with extreme insolubility [6] Later investigations corroborated these inferences and showed that the site of their formation is the endoplasmic reticulum (ER) [2,7,8,9]

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