The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Enhanced arsenate reduction by a CDC25‐like tyrosine phosphatase explains increased phytochelatin accumulation in arsenate‐tolerant Holcus lanatus
Open accessAbstract
Summary: Decreased arsenate [As(V)] uptake is the major mechanism of naturally selected As(V) hypertolerance in plants. However, As(V)‐hypertolerant ecotypes also show enhanced rates of phytochelatin (PC) accumulation, suggesting that improved sequestration might additionally contribute to the hypertolerance phenotype. Here, we show that enhanced PC‐based sequestration in As(V)‐hypertolerant Holcus lanatus is not due to an enhanced capacity for PC synthesis as such, but to increased As(V) reductase activity. Vacuolar transport of arsenite‐thiol complexes was equal in both ecotypes. Based on homology with the yeast As(V) reductase, Acr2p, we identified a Cdc25‐like plant candidate, HlAsr, and confirmed the As(V) reductase activity of both HlAsr and the homologous protein from Arabidopsis thaliana. The gene appeared to be As(V)‐inducible and its expression was enhanced in the As(V)‐hypertolerant H. lanatus ecotype, compared with the non‐tolerant ecotype. Homologous ectopic overexpression of the At ASR cDNA in A. thaliana produced a dual phenotype. It improved tolerance to mildly toxic levels of As(V) exposure, but caused hypersensitivity to more toxic levels. Arabidopsis asr T‐DNA mutants showed increased As(V) sensitivity at low exposure levels and enhanced arsenic retention in the root. It is argued that, next to decreased uptake, enhanced expression of Hl ASR might act as an additional determinant of As(V) hypertolerance and As transport in H. lanatus.
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Citations
Cites
Mechanism of Heavy Metal Ion Activation of Phytochelatin (PC) Synthase
Vatamaniuk, O. K., Mari, S., Lu, Y.-P., & Rea, P. A. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m002997200 · Cited by 390 · cited 2×
“, 2003) and form the As(III)-GS3 complex, the high-affinity substrate for PCS (Vatamaniuk et al., 2000).”
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Cited by
Zhao, F.-J., McGrath, S. P., & Meharg, A. A. (2010) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042809-112152 · Cited by 1,246
Arsenic uptake and metabolism in plants
Zhao, F. J., Ma, J. F., Meharg, A. A., & McGrath, S. P. (2009) · New Phytologist · doi:10.1111/j.1469-8137.2008.02716.x · Cited by 1,185
Arsenic Toxicity: The Effects on Plant Metabolism
Finnegan, P. M., & Chen, W. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00182 · Cited by 849
Arsenic tolerance in Arabidopsis is mediated by two ABCC-type phytochelatin transporters
Song, W.-Y., Park, J., Mendoza-Cózatl, D. G., Suter-Grotemeyer, M., Shim, D., Hörtensteiner, S., Geisler, M., Weder, B., Rea, P. A., Rentsch, D., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1013964107 · Cited by 667
Arsenic hazards: strategies for tolerance and remediation by plants
Tripathi, R. D., Srivastava, S., Mishra, S., Singh, N., Tuli, R., Gupta, D. K., & Maathuis, F. J. M. (2007) · Trends in Biotechnology · doi:10.1016/j.tibtech.2007.02.003 · Cited by 664
Metadata
- Authors
- Bleeker, P. M., Hakvoort, H. W. J., Bliek, M., Souer, E., & Schat, H.
- Venue
- The Plant Journal
- Publisher
- Wiley
- Published
- 2006-02-09
- Volume
- 45
- Issue
- 6
- Pages
- 917-929
- ISSN
- 0960-7412 (ISSN-L)
- 1365-313X
- OpenAlex
- W2044337579
- Cited by
- 256
- References
- 1
- FWCI
- 13.92
- Type
- journal article
- Language
- en
- Open access
- bronze
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- CoChat. (2026). Citation check: Enhanced arsenate reduction by a CDC25‐like tyrosine phosphatase explains increased phytochelatin accumulation in arsenate‐tolerant Holcus lanatus. https://app.cochat.ai/papers/10.1111/j.1365-313x.2005.02651.x
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- Bleeker, P. M., Hakvoort, H. W. J., Bliek, M., Souer, E., & Schat, H. (2006). Enhanced arsenate reduction by a CDC25‐like tyrosine phosphatase explains increased phytochelatin accumulation in arsenate‐tolerant Holcus lanatus. The Plant Journal. https://doi.org/10.1111/j.1365-313x.2005.02651.x
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