Investigation of ER to Golgi trafficking during mitosis

The secretory pathway facilitates movement of newly synthesized proteins (cargos) to the extracellular space to maintain cellular homeostasis. During interphase, secretory trafficking occurs for cellular function. In contrast, it has been long known that secretory trafficking is inhibited during mit...

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Main Author: Wong, Karuno Song Yao
Other Authors: Lu Lei
Format: Final Year Project
Language:English
Published: Nanyang Technological University 2023
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Online Access:https://hdl.handle.net/10356/172590
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spelling sg-ntu-dr.10356-1725902023-12-18T15:32:55Z Investigation of ER to Golgi trafficking during mitosis Wong, Karuno Song Yao Lu Lei School of Biological Sciences LULEI@ntu.edu.sg Science::Biological sciences::Molecular biology The secretory pathway facilitates movement of newly synthesized proteins (cargos) to the extracellular space to maintain cellular homeostasis. During interphase, secretory trafficking occurs for cellular function. In contrast, it has been long known that secretory trafficking is inhibited during mitosis. As the secretory transport pathway comprises multiple steps: endoplasmic reticulum (ER) to Golgi apparatus (hereafter Golgi), intra-Golgi, and post-Golgi trafficking, it is unclear which step is inhibited during mitosis. It is also unknown which stage of mitosis does ER-to-Golgi trafficking stops and resumes. In this study, we investigated if, and when ER-to-Golgi trafficking stops and resumes during mitosis. Through fluorescence imaging, we found colocalization of SBP-GFP-CD59 (RUSH - Retention Using Selective Hooks cargo) with mCherry-GM130 (cis-Golgi protein) during prophase and telophase but not from prometaphase-anaphase, indicating that ER-to-Golgi trafficking stops from prometaphase-anaphase and resumes in telophase. Furthermore, the morphology of Golgi in telophase cells was observed to resemble that of interphase cells. During prometaphase-anaphase, however, the Golgi appears as punctate structures, similar to mitotic Golgi clusters (MGCs). These results suggest that ER-to-Golgi trafficking occurs during telophase when the Golgi maintains a structure similar to the Golgi in interphase cells but is inhibited during prometaphase-anaphase when the Golgi appears as MGCs. Bachelor of Science in Biological Sciences 2023-12-15T01:44:47Z 2023-12-15T01:44:47Z 2023 Final Year Project (FYP) Wong, K. S. Y. (2023). Investigation of ER to Golgi trafficking during mitosis. Final Year Project (FYP), Nanyang Technological University, Singapore. https://hdl.handle.net/10356/172590 https://hdl.handle.net/10356/172590 en application/pdf Nanyang Technological University
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Biological sciences::Molecular biology
spellingShingle Science::Biological sciences::Molecular biology
Wong, Karuno Song Yao
Investigation of ER to Golgi trafficking during mitosis
description The secretory pathway facilitates movement of newly synthesized proteins (cargos) to the extracellular space to maintain cellular homeostasis. During interphase, secretory trafficking occurs for cellular function. In contrast, it has been long known that secretory trafficking is inhibited during mitosis. As the secretory transport pathway comprises multiple steps: endoplasmic reticulum (ER) to Golgi apparatus (hereafter Golgi), intra-Golgi, and post-Golgi trafficking, it is unclear which step is inhibited during mitosis. It is also unknown which stage of mitosis does ER-to-Golgi trafficking stops and resumes. In this study, we investigated if, and when ER-to-Golgi trafficking stops and resumes during mitosis. Through fluorescence imaging, we found colocalization of SBP-GFP-CD59 (RUSH - Retention Using Selective Hooks cargo) with mCherry-GM130 (cis-Golgi protein) during prophase and telophase but not from prometaphase-anaphase, indicating that ER-to-Golgi trafficking stops from prometaphase-anaphase and resumes in telophase. Furthermore, the morphology of Golgi in telophase cells was observed to resemble that of interphase cells. During prometaphase-anaphase, however, the Golgi appears as punctate structures, similar to mitotic Golgi clusters (MGCs). These results suggest that ER-to-Golgi trafficking occurs during telophase when the Golgi maintains a structure similar to the Golgi in interphase cells but is inhibited during prometaphase-anaphase when the Golgi appears as MGCs.
author2 Lu Lei
author_facet Lu Lei
Wong, Karuno Song Yao
format Final Year Project
author Wong, Karuno Song Yao
author_sort Wong, Karuno Song Yao
title Investigation of ER to Golgi trafficking during mitosis
title_short Investigation of ER to Golgi trafficking during mitosis
title_full Investigation of ER to Golgi trafficking during mitosis
title_fullStr Investigation of ER to Golgi trafficking during mitosis
title_full_unstemmed Investigation of ER to Golgi trafficking during mitosis
title_sort investigation of er to golgi trafficking during mitosis
publisher Nanyang Technological University
publishDate 2023
url https://hdl.handle.net/10356/172590
_version_ 1787136620804177920