Pregled bibliografske jedinice broj: 1074025
Quantitative structural organization of bulk apical membrane traffic in pollen tubes
Quantitative structural organization of bulk apical membrane traffic in pollen tubes // Plant physiology, 183 (2020), 4; 1559-1585 doi:10.1104/pp.20.00380 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1074025 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Quantitative structural organization of bulk
apical membrane traffic in pollen tubes
Autori
Grebnev, Gleb ; Cvitković, Mislav ; Fritz, Carolin ; Cai, Giampiero ; Smith, Ana-Sunčana ; Kost, Benedikt
Izvornik
Plant physiology (0032-0889) 183
(2020), 4;
1559-1585
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
structural organization ; membrane traffic ; polen tubes
Sažetak
Pollen tube tip growth depends on balancing secretion of cell wall material with endocytic recycling of excess material incorporated into the plasma membrane (PM). The classical model of tip growth, which predicts bulk secretion occurs apically and is compensated by subapical endocytosis, has been challenged in recent years. Many signaling proteins and lipids with important functions in the regulation of membrane traffic underlying tip growth associate with distinct regions of the pollen tube PM, and understanding the mechanisms responsible for the targeting of these regulatory factors to specific PM domains requires quantitative information concerning the sites of bulk secretion and endocytosis. Here, we quantitatively characterized the spatial organization of membrane traffic during tip growth by analyzing steady-state distributions and dynamics of FM4-64-labeled lipids and YFP-tagged transmembrane (TM) proteins in tobacco (Nicotiana tabacum) pollen tubes growing normally or treated with Brefeldin A to block secretion. We established that 1) secretion delivers TM proteins and recycled membrane lipids to the same apical PM domain, and 2) FM4-64-labeled lipids, but not the analyzed TM proteins, undergo endocytic recycling within a clearly defined subapical region. We mathematically modelled the steady- state PM distributions of all analyzed markers to better understand differences between them and to support the experimental data. Finally, we mapped subapical F-actin fringe and trans- Golgi network positioning relative to sites of bulk secretion and endocytosis to further characterize functions of these structures in apical membrane traffic. Our results support and further define the classical model of apical membrane traffic at the tip of elongating pollen tubes.
Izvorni jezik
Engleski
Znanstvena područja
Fizika
Napomena
FUNDING
Deutsche Forschungsgemeinschaft (DFG)
RTG 1962 P7
Gleb Grebnev, Benedikt Kost
Deutsche Forschungsgemeinschaft (DFG)
RTG 1962 P10
Mislav Cvitkovic, Ana-Suncana Smith
EC | European Research Council (ERC)
2013-33728
Mislav Cvitkovic, Ana-Suncana Smith
Deutsche Forschungsgemeinschaft (DFG)
INST90/1074-1FUGG
Benedikt Kost
Deutsche Forschungsgemeinschaft (DFG)
INST90/1025-1FUGG
Benedikt Kost
Poveznice na cjeloviti tekst rada:
Pristup cjelovitom tekstu rada doi www.plantphysiol.org fulir.irb.hrCitiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE