Cited by 139Polysaccharides and Plant Cell WallsGlycosylation and Glycoproteins ResearchCellular transport and secretion

The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.

The cellulose‐deficient Arabidopsis mutant rsw3 is defective in a gene encoding a putative glucosidase II, an enzyme processing N‐glycans during ER quality control

Open access

Abstract

Summary: rsw3 is a temperature‐sensitive mutant of Arabidopsis thaliana showing radially swollen roots and a deficiency in cellulose. The rsw3 gene was identified by a map‐based strategy, and shows high similarity to the catalytic α‐subunits of glucosidase II from mouse, yeast and potato. These enzymes process N‐linked glycans in the ER, so that they bind and then release chaperones as part of the quality control pathway, ensuring correct protein folding. Putative β‐subunits for the glucosidase II holoenzyme identified in the Arabidopsis and rice genomes share characteristic motifs (including an HDEL ER‐retention signal) with β‐subunits in mammals and yeast. The genes encoding the putative α‐ and β‐subunits are single copy and, like the rsw3 phenotype, widely expressed. rsw3 reduces cell number more strongly than cell size in stamen filaments and probably stems. Most features of the rsw3 phenotype are shared with other cellulose‐deficient mutants, but some – notably, production of multiple rosettes and a lack of secreted seed mucilage – are not and may reflect glucosidase II affecting processes other than cellulose synthesis. The rsw3 root phenotype develops more slowly than the rsw1 and rsw2 phenotypes when seedlings are transferred to the restrictive temperature. This is consistent with rsw3 reducing glycoprotein delivery from the ER to the plasma membrane whereas rsw1 and rsw2 act more rapidly by affecting the properties of already delivered enzymes.

Overview

Integrity signals

Registry

Crossref · 10.1046/j.1365-313x.2002.01483.x

Cites

4 of 4 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Verification

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Citations

Cites

Show all 4 references

Research works printed but not linked: 49

  1. 10.1093/glycob/10.5.487 · DOI
  2. 10.1126/science.279.5351.717 · DOI
  3. 10.1071/PP9920427 · DOI
  4. 10.1104/pp.116.4.1515 · DOI
  5. 10.1073/pnas.92.18.8259 · DOI
  6. 10.1093/emboj/20.5.1010 · DOI
  7. 10.1111/j.1432-1033.1984.tb08169.x · DOI · Paper page
  8. 10.1104/pp.010931 · DOI
  9. 10.1046/j.1365-313x.1998.00343.x · DOI
  10. 10.1074/jbc.274.36.25899 · DOI
  11. 10.1104/pp.010822 · DOI
  12. 10.1105/tpc.12.12.2409 · DOI
  13. 10.1023/A:1005925819741 · DOI
  14. 10.1104/pp.110.3.933 · DOI
  15. 10.1104/pp.114.1.295 · DOI
  16. 10.1083/jcb.200111093 · DOI
  17. 10.1126/science.291.5512.2364 · DOI · Paper page
  18. 10.1042/bj2800309 · DOI
  19. 10.1021/bi00324a040 · DOI
  20. Kaushal G.P., 1990, Purification to homogeneity and properties of glucosidase II from mung bean seedlings and suspension cultured soybean cells, J. Biol. Chem., 265, 16271, 10.1016/S0021-9258(17)46218-1 · DOI
  21. 10.1105/tpc.11.11.2075 · DOI
  22. 10.1104/pp.126.1.278 · DOI
  23. 10.1073/pnas.051625798 · DOI
  24. 10.1126/science.252.5009.1162 · DOI · Paper page
  25. 10.1104/pp.010269 · DOI
  26. 10.1104/pp.119.2.385 · DOI
  27. 10.1111/j.1399-3054.1962.tb08052.x · DOI
  28. 10.1093/emboj/17.19.5563 · DOI
  29. 10.1105/tpc.6.11.1567 · DOI
  30. 10.1105/tpc.11.12.2263 · DOI
  31. 10.1007/s004250000301 · DOI
  32. 10.1126/science.1064281 · DOI
  33. 10.1016/S0092-8674(00)81192-7 · DOI
  34. 10.1093/pcp/pce045 · DOI
  35. 10.1073/pnas.191361598 · DOI
  36. 10.1104/pp.90.2.708 · DOI
  37. 10.1007/BF01280312 · DOI
  38. 10.1105/tpc.12.12.2529 · DOI
  39. 10.1046/j.1365-313x.2000.00873.x · DOI
  40. 10.1105/tpc.11.5.769 · DOI
  41. 10.1093/glycob/10.5.493 · DOI · Paper page
  42. 10.1021/bi010629u · DOI
  43. 10.1074/jbc.271.44.27509 · DOI · Paper page
  44. Vitale A., 2001, Uncovering secretory secrets: inhibition of endoplasmic reticulum (ER) glucosidases suggests a critical role of ER quality control in plant growth and development, Plant Cell, 13, 1260
  45. 10.1104/pp.010410 · DOI
  46. 10.1104/pp.122.2.345 · DOI
  47. 10.1007/BF01280308 · DOI
  48. 10.1007/PL00000790 · DOI
  49. 10.1105/tpc.12.7.1137 · DOI

Cited by

Sorted by citations

See all 139

Metadata

Authors
Burn, J. E., Hurley, U. A., Birch, R. J., Arioli, T., Cork, A., & Williamson, R. E.
Affiliations
Australian National University (AU)
Corresponding author
Williamson, Richard E.
Venue
The Plant Journal
Publisher
Wiley
Published
2002-12
Volume
32
Issue
6
Pages
949-960
ISSN
  • 0960-7412 (ISSN-L)
  • 1365-313X
OpenAlex
W2046407819
Cited by
139
References
4
Citations by year
2026: 3 · 2025: 2 · 2024: 2 · 2023: 1 · 2022: 6 · 2021: 4 · 2020: 3 · 2019: 1 · 2018: 8 · 2017: 2 · 2016: 6 · 2015: 8 · 2014: 10 · 2013: 5 · 2012: 6
FWCI
5.89
Type
journal article
Language
en
Open access
Locations
  • The Plant Journal (publishedVersion)
  • PubMed (publishedVersion)
  • ANU Open Research (Australian National University) (submittedVersion)
Funders
Cotton Research and Development Corporation
Topics
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Polysaccharides and Plant Cell Walls
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Glycosylation and Glycoproteins Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
Keywords
glucosidase II, N-glycan processing, ER quality control, temperature-sensitive mutants, Arabidopsis thaliana, beta subunit, protein folding, seed mucilage, root development, stamen filaments
MeSH terms
alpha-Glucosidases, Amino Acid Sequence, Cell Division, Cellulose, Endoplasmic Reticulum, Fertility, Glucans, Glucosyltransferases, Microscopy, Electron, Scanning, Molecular Sequence Data, Mutation, Phenotype, Protein Conformation, Oryza, Temperature, Conserved Sequence, Arabidopsis, Sequence Homology, Amino Acid, Plant Roots, Arabidopsis Proteins, Flowers

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: The cellulose‐deficient Arabidopsis mutant rsw3 is defective in a gene encoding a putative glucosidase II, an enzyme processing N‐glycans during ER quality control. https://app.cochat.ai/papers/10.1046/j.1365-313x.2002.01483.x
The paper
Burn, J. E., Hurley, U. A., Birch, R. J., Arioli, T., Cork, A., & Williamson, R. E. (2002). The cellulose‐deficient Arabidopsis mutant rsw3 is defective in a gene encoding a putative glucosidase II, an enzyme processing N‐glycans during ER quality control. The Plant Journal. https://doi.org/10.1046/j.1365-313x.2002.01483.x