Evidence map›Paper›PMID 24795147›Full record

ArticleBiology open2014

GRASP65 controls the cis Golgi integrity in vivo.

Tineke Veenendaal, Tim Jarvela, Adam G Grieve, Johan H van Es, Adam D Linstedt, Catherine Rabouille

Abstract read
In one paragraph

Article in Biology open, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

  1. Article
  2. A biallelic variant inLife science alliance · 2025
    Article
  3. Article
  4. Article
  5. Golgi defect as a major contributor to lysosomal dysfunction.Frontiers in cell and developmental biology · 2024
    Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. GRASPing for consensus about the Golgi apparatus.The Journal of cell biology · 2021
    Article
  11. Article
  12. Review
  13. Article
  14. Grasp55Nature communications · 2020
    Article
  15. Unlocking Golgi: Why Does Morphology Matter?Biochemistry. Biokhimiia · 2019
    Review
  16. Article
  17. Article
  18. New Insights Into the Golgi Stacking Proteins.Frontiers in cell and developmental biology · 2019
    Review
  19. A New Look at the Functional Organization of the Golgi Ribbon.Frontiers in cell and developmental biology · 2019
    Article
  20. Review
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

6 authors.

Tineke VeenendaalHubrecht Institute-KNAW and University Medical Center Utrecht, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.
Tim JarvelaDepartment of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Adam G GrieveHubrecht Institute-KNAW and University Medical Center Utrecht, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands Present address: Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, UK.
Johan H van EsHubrecht Institute-KNAW and University Medical Center Utrecht, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands.
Adam D LinstedtDepartment of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Catherine RabouilleHubrecht Institute-KNAW and University Medical Center Utrecht, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands Department of Cell Biology, University Medical Center Utrecht, Heidelberglaan 100, 3584 CX Utrecht, The Netherlands c.rabouille@hubrecht.eu.

Funding

STRUCTURAL BASIS OF ORGANELLE TETHERINGR01GM095549 · NIGMS · CARNEGIE-MELLON UNIVERSITY · PI LINSTEDT, ADAM D · 2011 to 2014
$1.2M
NIGMS NIH HHS R01 GM095549
6 · The paper itself

Abstract

GRASP65 and GRASP55 are peripheral Golgi proteins localized to cis and medial/trans cisternae, respectively. They are implicated in diverse aspects of protein transport and structure related to the Golgi complex, including the stacking of the Golgi stack and/or the linking of mammalian Golgi stacks into the Golgi ribbon. Using a mouse model, we interfered with GRASP65 by homologous recombination and confirmed its absence of expression. Surprisingly, the mice were healthy and fertile with no apparent defects in tissue, cellular or subcellular organization. Immortalized MEFs derived from the mice did not show any growth or morphological defects. However, despite the normal appearance of the Golgi ribbon, a fluorescence recovery after photobleaching assay revealed functional discontinuities specific to the cis cisternal membrane network. This leads to a strong change in the plasma membrane GSII lectin staining that was also observed in certain mutant tissues. These findings substantiate the role of GRASP65 in continuity of the cis Golgi network required for proper glycosylation, while showing that neither this continuity nor GRASP65 itself are essential for the viability of a complex organism.

Indexed as

Expression patternFRAPGlycosylationGolgiGolgi ribbon linkingGORASPGRASP55GRASP65Knock-in mouse

Identifiers

PMID24795147
PMCPMC4058077

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.