Evidence map›Paper›PMID 41240316›Full record

ReviewSub-cellular biochemistry2026

Cisternal Maturation of the Golgi Apparatus in Budding Yeast.

Takuro Tojima, Akihiko Nakano

Abstract readReview
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In one paragraph

Review in Sub-cellular biochemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Takuro TojimaRIKEN Center for Advanced Photonics, Wako, Saitama, Japan. takuro.tojima@riken.jp.
Akihiko NakanoRIKEN Center for Advanced Photonics, Wako, Saitama, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Golgi ApparatusSaccharomycetalesMicroscopy, ElectronProtein TransportCisternal maturationER-Golgi intermediate compartment (ERGIC)Golgi apparatusLive cell imagingSaccharomyces cerevisiaetrans-Golgi network (TGN)

Identifiers

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.