The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Storage Protein Accumulation in the Absence of the Vacuolar Processing Enzyme Family of Cysteine Proteases[W]
Open accessAbstract
The role(s) of specific proteases in seed protein processing is only vaguely understood; indeed, the overall role of processing in stable protein deposition has been the subject of more speculation than direct investigation. Seed-type members of the vacuolar processing enzyme (VPE) family were hypothesized to perform a unique function in seed protein processing, but we demonstrated previously that Asn-specific protein processing in developing Arabidopsis seeds occurs independently of this VPE activity. Here, we describe the unexpected expression of vegetative-type VPEs in developing seeds and test the role(s) of all VPEs in seed storage protein accumulation by systematically stacking knockout mutant alleles of all four members (αVPE, βVPE, γVPE, and δVPE) of the VPE gene family in Arabidopsis. The complete removal of VPE function in the αvpe βvpe γvpe δvpe quadruple mutant resulted in a total shift of storage protein accumulation from wild-type processed polypeptides to a finite number of prominent alternatively processed polypeptides cleaved at sites other than the conserved Asn residues targeted by VPE. Although alternatively proteolyzed legumin-type globulin polypeptides largely accumulated as intrasubunit disulfide-linked polypeptides with apparent molecular masses similar to those of VPE-processed legumin polypeptides, they showed markedly altered solubility and protein assembly characteristics. Instead of forming 11S hexamers, alternatively processed legumin polypeptides were deposited primarily as 9S complexes. However, despite the impact on seed protein processing, plants devoid of all known functional VPE genes appeared unchanged with regard to protein content in mature seeds, relative mobilization rates of protein reserves during germination, and vegetative growth. These findings indicate that VPE-mediated Asn-specific proteolytic processing, and the physiochemical property changes attributed to this specific processing step, are not required for the successful deposition and mobilization of seed storage protein in the protein storage vacuoles of Arabidopsis seeds.
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Citations
Cites
Measurement of protein using bicinchoninic acid
Smith, P. K., Krohn, R. I., Hermanson, G. T., Mallia, A. K., Gartner, F. H., Provenzano, M. D., Fujimoto, E. K., Goeke, N. M., Olson, B. J., & Klenk, D. C. (1985) · Analytical Biochemistry · doi:10.1016/0003-2697(85)90442-7 · Cited by 18,482
Gene expression analysis by massively parallel signature sequencing (MPSS) on microbead arrays.
Brenner, S., Johnson, M., Bridgham, J., Golda, G., Lloyd, D. H., Johnson, D., Luo, S., McCurdy, S., Foy, M., Ewan, M., et al. (2000) · Nature Biotechnology · doi:10.1038/76469 · Cited by 1,360
Cited by
Panel), E. P. O. G. M. O. (. (2010) · EFSA Journal · doi:10.2903/j.efsa.2010.1700 · Cited by 608
Patterns of Protein Oxidation in Arabidopsis Seeds and during Germination
Job, C., Rajjou, L., Lovigny, Y., Belghazi, M., & Job, D. (2005) · Plant Physiology · doi:10.1104/pp.105.062778 · Cited by 401
A cut above the rest: the regulatory function of plant proteases
Schaller, A. (2004) · Planta · doi:10.1007/s00425-004-1407-2 · Cited by 384
Storage Reserve Accumulation in Arabidopsis: Metabolic and Developmental Control of Seed Filling
Baud, S., Dubreucq, B., Miquel, M., Rochat, C., & Lepiniec, L. (2008) · The Arabidopsis Book · doi:10.1199/tab.0113 · Cited by 288
Structure and function of legumain in health and disease
Dall, E., & Brandstetter, H. (2016) · Biochimie · doi:10.1016/j.biochi.2015.09.022 · Cited by 281
Metadata
- Authors
- Gruis, D., Schulze, J., & Jung, R.
- Venue
- The Plant Cell
- Publisher
- Oxford University Press (OUP)
- Published
- 2004-01-01
- Volume
- 16
- Issue
- 1
- Pages
- 270-290
- ISSN
- 1040-4651 (ISSN-L)
- 1532-298X
- OpenAlex
- W2106190285
- Cited by
- 164
- References
- 2
- FWCI
- 12.37
- Type
- journal article
- Language
- en
- Open access
- green
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