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NtGNL1 Plays an Essential Role in Pollen Tube Tip Growth and Orientation Likely via Regulation of Post-Golgi Trafficking

BACKGROUND: Tobacco GNOM LIKE 1 (NtGNL1), a new member of the Big/GBF family, is characterized by a sec 7 domain. Thus, we proposed that NtGNL1 may function in regulating pollen tube growth for vesicle trafficking. METHODOLOGY/PRINCIPAL FINDINGS: To test this hypothesis, we used an RNAi technique to...

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Detalles Bibliográficos
Autores principales: Liao, Fanglei, Wang, Lu, Yang, Li-Bo, Peng, Xiongbo, Sun, Mengxiang
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955533/
https://www.ncbi.nlm.nih.gov/pubmed/20976165
http://dx.doi.org/10.1371/journal.pone.0013401
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author Liao, Fanglei
Wang, Lu
Yang, Li-Bo
Peng, Xiongbo
Sun, Mengxiang
author_facet Liao, Fanglei
Wang, Lu
Yang, Li-Bo
Peng, Xiongbo
Sun, Mengxiang
author_sort Liao, Fanglei
collection PubMed
description BACKGROUND: Tobacco GNOM LIKE 1 (NtGNL1), a new member of the Big/GBF family, is characterized by a sec 7 domain. Thus, we proposed that NtGNL1 may function in regulating pollen tube growth for vesicle trafficking. METHODOLOGY/PRINCIPAL FINDINGS: To test this hypothesis, we used an RNAi technique to down-regulate NtGNL1 expression and found that pollen tube growth and orientation were clearly inhibited. Cytological observations revealed that both timing and behavior of endocytosis was disrupted, and endosome trafficking to prevacuolar compartments (PVC) or multivesicular bodies (MVB) was altered in pollen tube tips. Moreover, NtGNL1 seemed to partially overlap with Golgi bodies, but clearly colocalized with putative late endosome compartments. We also observed that in such pollen tubes, the Golgi apparatus disassembled and fused with the endoplasmic reticulum, indicating abnormal post-Golgi trafficking. During this process, actin organization was also remodeled. CONCLUSIONS/SIGNIFICANCE: Thus, we revealed that NtGNL1 is essential for pollen tube growth and orientation and it likely functions via stabilizing the structure of the Golgi apparatus and ensuring post-Golgi trafficking.
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spelling pubmed-29555332010-10-25 NtGNL1 Plays an Essential Role in Pollen Tube Tip Growth and Orientation Likely via Regulation of Post-Golgi Trafficking Liao, Fanglei Wang, Lu Yang, Li-Bo Peng, Xiongbo Sun, Mengxiang PLoS One Research Article BACKGROUND: Tobacco GNOM LIKE 1 (NtGNL1), a new member of the Big/GBF family, is characterized by a sec 7 domain. Thus, we proposed that NtGNL1 may function in regulating pollen tube growth for vesicle trafficking. METHODOLOGY/PRINCIPAL FINDINGS: To test this hypothesis, we used an RNAi technique to down-regulate NtGNL1 expression and found that pollen tube growth and orientation were clearly inhibited. Cytological observations revealed that both timing and behavior of endocytosis was disrupted, and endosome trafficking to prevacuolar compartments (PVC) or multivesicular bodies (MVB) was altered in pollen tube tips. Moreover, NtGNL1 seemed to partially overlap with Golgi bodies, but clearly colocalized with putative late endosome compartments. We also observed that in such pollen tubes, the Golgi apparatus disassembled and fused with the endoplasmic reticulum, indicating abnormal post-Golgi trafficking. During this process, actin organization was also remodeled. CONCLUSIONS/SIGNIFICANCE: Thus, we revealed that NtGNL1 is essential for pollen tube growth and orientation and it likely functions via stabilizing the structure of the Golgi apparatus and ensuring post-Golgi trafficking. Public Library of Science 2010-10-15 /pmc/articles/PMC2955533/ /pubmed/20976165 http://dx.doi.org/10.1371/journal.pone.0013401 Text en Liao et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Liao, Fanglei
Wang, Lu
Yang, Li-Bo
Peng, Xiongbo
Sun, Mengxiang
NtGNL1 Plays an Essential Role in Pollen Tube Tip Growth and Orientation Likely via Regulation of Post-Golgi Trafficking
title NtGNL1 Plays an Essential Role in Pollen Tube Tip Growth and Orientation Likely via Regulation of Post-Golgi Trafficking
title_full NtGNL1 Plays an Essential Role in Pollen Tube Tip Growth and Orientation Likely via Regulation of Post-Golgi Trafficking
title_fullStr NtGNL1 Plays an Essential Role in Pollen Tube Tip Growth and Orientation Likely via Regulation of Post-Golgi Trafficking
title_full_unstemmed NtGNL1 Plays an Essential Role in Pollen Tube Tip Growth and Orientation Likely via Regulation of Post-Golgi Trafficking
title_short NtGNL1 Plays an Essential Role in Pollen Tube Tip Growth and Orientation Likely via Regulation of Post-Golgi Trafficking
title_sort ntgnl1 plays an essential role in pollen tube tip growth and orientation likely via regulation of post-golgi trafficking
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955533/
https://www.ncbi.nlm.nih.gov/pubmed/20976165
http://dx.doi.org/10.1371/journal.pone.0013401
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