{"title":"Cisternal Maturation of the Golgi Apparatus in Budding Yeast.","authors":"Takuro Tojima, Akihiko Nakano","doi":"10.1007/978-3-032-06936-8_12","DOIUrl":null,"url":null,"abstract":"<p><p>The Golgi apparatus in the budding yeast Saccharomyces cerevisiae, unlike those in mammalian and plant cells, does not form stacks but exists as multiple separate cisternae scattered throughout the cytoplasm. This unique morphological feature has allowed us to observe the spatiotemporal dynamics of individual Golgi cisternae by live cell imaging. Nearly two decades ago, we developed super-resolution confocal live imaging microscopy (SCLIM) and visualized that the yeast Golgi truly matures, i.e., a single cisterna gradually changes its nature from cis to trans cisternae over time. Since then to date, many researchers have observed a wide variety of proteins residing in and around the Golgi, as well as cargoes, in live yeast cells, unveiling the detailed step-by-step processes of Golgi cisternal maturation. Notably, our recent studies identified the ER-Golgi intermediate compartment (ERGIC) in budding yeast, which matures into the cis Golgi. After cis-to-trans maturation, the trans Golgi further matures into the trans-Golgi network (TGN), which can be divided into at least two sub-stages, the early and late TGN. Altogether, accumulating evidence revealed that the Golgi apparatus is not a static, but rather a highly dynamic organelle that appears transiently with a short lifetime along with cargo traffic.</p>","PeriodicalId":21991,"journal":{"name":"Sub-cellular biochemistry","volume":"110 ","pages":"287-311"},"PeriodicalIF":0.0000,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sub-cellular biochemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/978-3-032-06936-8_12","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0
Abstract
The Golgi apparatus in the budding yeast Saccharomyces cerevisiae, unlike those in mammalian and plant cells, does not form stacks but exists as multiple separate cisternae scattered throughout the cytoplasm. This unique morphological feature has allowed us to observe the spatiotemporal dynamics of individual Golgi cisternae by live cell imaging. Nearly two decades ago, we developed super-resolution confocal live imaging microscopy (SCLIM) and visualized that the yeast Golgi truly matures, i.e., a single cisterna gradually changes its nature from cis to trans cisternae over time. Since then to date, many researchers have observed a wide variety of proteins residing in and around the Golgi, as well as cargoes, in live yeast cells, unveiling the detailed step-by-step processes of Golgi cisternal maturation. Notably, our recent studies identified the ER-Golgi intermediate compartment (ERGIC) in budding yeast, which matures into the cis Golgi. After cis-to-trans maturation, the trans Golgi further matures into the trans-Golgi network (TGN), which can be divided into at least two sub-stages, the early and late TGN. Altogether, accumulating evidence revealed that the Golgi apparatus is not a static, but rather a highly dynamic organelle that appears transiently with a short lifetime along with cargo traffic.
期刊介绍:
The book series SUBCELLULAR BIOCHEMISTRY is a renowned and well recognized forum for disseminating advances of emerging topics in Cell Biology and related subjects. All volumes are edited by established scientists and the individual chapters are written by experts on the relevant topic. The individual chapters of each volume are fully citable and indexed in Medline/Pubmed to ensure maximum visibility of the work.