ER sensing of lipid metabolism drives PRA family-dependent regulation of COPII vesicle transport

Newly synthesized secretory proteins and many lipids are transported from the endoplasmic reticulum (ER) to the Golgi prior to their ultimate destinations. The ER-to-Golgi transport must be tightly regulated during adaptation to environmental stress. However, the sensing mechanism and regulatory pat...

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Main Authors Nakazato, Mitsuki, Nakamura, Hiroki, Kato, Mei, Ikema, Ryoko, Iguchi, Mizuki, Hanaoka, Kazuki, Eto, Katsuki, Karashima, Takefumi, Ikeda, Atsuko, Yabuki, Yukari, Schlarmann, Philipp, Manzano-Lopez, Javier, Aguilera-Romero, Auxiliadora, Sabido-Bozo, Susana, Perez-Linero, Ana Maria, Kana, Muneyoshi, Iefuji, Haruyuki, Riezman, Isabelle, Riezman, Howard, Muniz, Manuel, Funato, Kouichi
Format Paper
LanguageEnglish
Published Cold Spring Harbor Cold Spring Harbor Laboratory Press 11.11.2024
Cold Spring Harbor Laboratory
Edition1.1
Subjects
Cell Biology
Endoplasmic reticulum
Environmental stress
Golgi apparatus
Lipid composition
Lipid metabolism
Membrane trafficking
Phosphatidic acid
Protein transport
Yip3
COPII-mediated trafficking
Opi1
Membrane lipid
Ino2/Ino4 transcriptional activator
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Abstract Newly synthesized secretory proteins and many lipids are transported from the endoplasmic reticulum (ER) to the Golgi prior to their ultimate destinations. The ER-to-Golgi transport must be tightly regulated during adaptation to environmental stress. However, the sensing mechanism and regulatory pathways governing the consecutive formation, budding and transportation of COPII vesicles from the ER remain insufficiently explored. Here, we present evidence indicating that COPII-mediated vesicle transport is transcriptionally controlled through the phosphatidic acid-dependent Opi1-Ino2/Ino4 regulatory circuit. Our analysis indicates that YIP3, a target gene of Ino2/Ino4, exerts a negative regulatory impact on COPII-mediated vesicle transport. Furthermore, we demonstrated that Ino2/Ino4 but not Yip3 modulates Sar1 activation, the initial step in COPII vesicle formation, whereas Yip3 hinders Sec16 assembly on the ER membrane, thereby implying that Ino2/Ino4 governs COPII-mediated trafficking at multiple steps. Thus, this study provides the first evidence for an ER sensing system that transcriptionally fine-tunes multiple steps of anterograde vesicular transport in response to alterations in lipid composition of the ER membrane.
AbstractList Newly synthesized secretory proteins and many lipids are transported from the endoplasmic reticulum (ER) to the Golgi prior to their ultimate destinations. The ER-to-Golgi transport must be tightly regulated during adaptation to environmental stress. However, the sensing mechanism and regulatory pathways governing the consecutive formation, budding and transportation of COPII vesicles from the ER remain insufficiently explored. Here, we present evidence indicating that COPII-mediated vesicle transport is transcriptionally controlled through the phosphatidic acid-dependent Opi1-Ino2/Ino4 regulatory circuit. Our analysis indicates that YIP3, a target gene of Ino2/Ino4, exerts a negative regulatory impact on COPII-mediated vesicle transport. Furthermore, we demonstrated that Ino2/Ino4 but not Yip3 modulates Sar1 activation, the initial step in COPII vesicle formation, whereas Yip3 hinders Sec16 assembly on the ER membrane, thereby implying that Ino2/Ino4 governs COPII-mediated trafficking at multiple steps. Thus, this study provides the first evidence for an ER sensing system that transcriptionally fine-tunes multiple steps of anterograde vesicular transport in response to alterations in lipid composition of the ER membrane.
Author Iefuji, Haruyuki
Funato, Kouichi
Riezman, Howard
Riezman, Isabelle
Muniz, Manuel
Sabido-Bozo, Susana
Kana, Muneyoshi
Hanaoka, Kazuki
Perez-Linero, Ana Maria
Nakazato, Mitsuki
Schlarmann, Philipp
Ikema, Ryoko
Iguchi, Mizuki
Karashima, Takefumi
Ikeda, Atsuko
Manzano-Lopez, Javier
Kato, Mei
Aguilera-Romero, Auxiliadora
Nakamura, Hiroki
Yabuki, Yukari
Eto, Katsuki
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Keywords Yip3
COPII-mediated trafficking
Opi1
Membrane lipid
Ino2/Ino4 transcriptional activator
Language English
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Snippet Newly synthesized secretory proteins and many lipids are transported from the endoplasmic reticulum (ER) to the Golgi prior to their ultimate destinations. The...
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proquest
SourceType Open Access Repository
Aggregation Database
SubjectTerms Cell Biology
Endoplasmic reticulum
Environmental stress
Golgi apparatus
Lipid composition
Lipid metabolism
Membrane trafficking
Phosphatidic acid
Protein transport
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Title ER sensing of lipid metabolism drives PRA family-dependent regulation of COPII vesicle transport
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