Abstract
Cellulose is synthesized at the plasma membrane by the cellulose synthase complex, a structure that contains three distinct isoforms of the catalytic subunit, cellulose synthase A (CESA). The division into three subunits appears early in land plant evolution and is highly conserved, particularly for the secondary cell wall. However, what if any unique roles each isoform plays in the complex remain unclear. Here, we assessed the contributions of specific isoforms to microfibril synthesis. First, we expressed CESA isoforms of the primary cell wall or the moss Physcomitrium patens in Arabidopsis thaliana backgrounds missing a secondary cell wall CESA. While the primary cell wall isoforms rescued the cesa knockout phenotype with partial isoform specificity, those from the moss rescued with fewer restrictions. Then, we recreated various CESA missense mutations in all three of the secondary cell wall isoforms; while results are consistent with isoform specificity, they are difficult to interpret further without molecular structures. Finally, we show that catalytically inactive CESA isoforms restore growth and cellulose content in the corresponding knockout in an isoform-specific manner; along with partial rescue of the growth and cellulose content of the inflorescence stem, the replacement lines have fiber cells with partially disorganized microfibrils and secondary cell wall cellulose with narrow crystal width. Generally, effects were more pronounced in lines where CESA8 was inactivated compared with inactivating CESA4 or 7, which tended to have similar phenotypes to each other. We account for these results with a model for cellulose synthase structure with the isoforms assigned specific localization within the cellulose synthase complex.
| Original language | English |
|---|---|
| Article number | e70344 |
| Journal | Plant Journal |
| Volume | 123 |
| Issue number | 2 |
| DOIs | |
| State | Published - Jul 2025 |
Funding
We lament the untimely passing of Dr. Janna Maranas, who contributed to the SANS analysis. We thank Dr. Alison Roberts (University of Rhode Island) for the gift of all PpCESA cDNAs, Dr. Ying Gu (Penn State) for the gift of AtCESA6 and AtCESA8 cDNA, and the Salk Institute Genomic Analysis Laboratory for providing the sequence‐indexed T‐DNA insertion mutants. Funding for the SIGnAL indexed insertion mutant collection (or cDNA/ORFeome collection) was provided by the National Science Foundation. Scanning electron microscopy was supported by the Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences of the U.S. Department of Energy (grant no. DE‐FG‐03ER15421 to the laboratory of T.I.B). All other aspects of this work were supported by the Center for Lignocellulose Structure and Formation, an Energy Frontier Research Center funded by the US Department of Energy, Office of Science, Basic Energy Sciences under award DE‐SC0001090. A. thaliana We lament the untimely passing of Dr. Janna Maranas, who contributed to the SANS analysis. We thank Dr. Alison Roberts (University of Rhode Island) for the gift of all PpCESA cDNAs, Dr. Ying Gu (Penn State) for the gift of AtCESA6 and AtCESA8 cDNA, and the Salk Institute Genomic Analysis Laboratory for providing the sequence-indexed A. thaliana T-DNA insertion mutants. Funding for the SIGnAL indexed insertion mutant collection (or cDNA/ORFeome collection) was provided by the National Science Foundation. Scanning electron microscopy was supported by the Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences of the U.S. Department of Energy (grant no. DE-FG-03ER15421 to the laboratory of T.I.B). All other aspects of this work were supported by the Center for Lignocellulose Structure and Formation, an Energy Frontier Research Center funded by the US Department of Energy, Office of Science, Basic Energy Sciences under award DE-SC0001090.
Keywords
- Arabidopsis thaliana
- Physomitrium patens
- X-ray diffraction
- cellulose
- cellulose content
- cellulose synthase A
- field-emission scanning electron microscopy
- neutron scattering
- secondary cell wall
- stem height