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. 1996 Apr;110(4):1109–1121. doi: 10.1104/pp.110.4.1109

Hormonal Studies of fass, an Arabidopsis Mutant That Is Altered in Organ Elongation.

R H Fisher 1, M K Barton 1, J D Cohen 1, T J Cooke 1
PMCID: PMC160891  PMID: 12226245

Abstract

We have isolated an allele of fass, an Arabidopsis thaliana mutation that separates plant development and organ differentiation from plant elongation, and studied its hormonal regulation. Micro-surgically isolated fass roots elongate 2.5 times as much as the roots on intact mutant plants. Wild-type heart embryos, when cultured with a strong auxin, naphthaleneacetic acid, phenocopy fass embryos. fass seedlings contain variable levels of free auxin, which average 2.5 times higher than wild-type seedling levels, and fass seedlings evolve 3 times as much ethylene as wild-type seedlings on a per-plant basis over a 24-h period. The length-to-width ratios of fass seedlings can be changed by several compounds that affect their endogenous ethylene levels, but fass is epistatic to etr1, an ethylene-insensitive mutant. fass's high levels of free auxin may be inducing its high levels of ethylene, which may, in turn, result in the fass phenotype. We postulate that FASS may be acting as a negative regulator to maintain wild-type auxin levels and that the mutation may be in an auxin-conjugating enzyme.

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Selected References

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  1. Blancaflor E. B., Hasenstein K. H. Time course and auxin sensitivity of cortical microtubule reorientation in maize roots. Protoplasma. 1995;185:72–82. doi: 10.1007/BF01272755. [DOI] [PubMed] [Google Scholar]
  2. Boerjan W., Cervera M. T., Delarue M., Beeckman T., Dewitte W., Bellini C., Caboche M., Van Onckelen H., Van Montagu M., Inzé D. Superroot, a recessive mutation in Arabidopsis, confers auxin overproduction. Plant Cell. 1995 Sep;7(9):1405–1419. doi: 10.1105/tpc.7.9.1405. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Chang C., Kwok S. F., Bleecker A. B., Meyerowitz E. M. Arabidopsis ethylene-response gene ETR1: similarity of product to two-component regulators. Science. 1993 Oct 22;262(5133):539–544. doi: 10.1126/science.8211181. [DOI] [PubMed] [Google Scholar]
  4. Ecker J. R. The ethylene signal transduction pathway in plants. Science. 1995 May 5;268(5211):667–675. doi: 10.1126/science.7732375. [DOI] [PubMed] [Google Scholar]
  5. Hua J., Chang C., Sun Q., Meyerowitz E. M. Ethylene insensitivity conferred by Arabidopsis ERS gene. Science. 1995 Sep 22;269(5231):1712–1714. doi: 10.1126/science.7569898. [DOI] [PubMed] [Google Scholar]
  6. Jürgens G., Torres Ruiz R. A., Berleth T. Embryonic pattern formation in flowering plants. Annu Rev Genet. 1994;28:351–371. doi: 10.1146/annurev.ge.28.120194.002031. [DOI] [PubMed] [Google Scholar]
  7. Kieber J. J., Rothenberg M., Roman G., Feldmann K. A., Ecker J. R. CTR1, a negative regulator of the ethylene response pathway in Arabidopsis, encodes a member of the raf family of protein kinases. Cell. 1993 Feb 12;72(3):427–441. doi: 10.1016/0092-8674(93)90119-b. [DOI] [PubMed] [Google Scholar]
  8. King J. J., Stimart D. P., Fisher R. H., Bleecker A. B. A Mutation Altering Auxin Homeostasis and Plant Morphology in Arabidopsis. Plant Cell. 1995 Dec;7(12):2023–2037. doi: 10.1105/tpc.7.12.2023. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Lincoln C., Britton J. H., Estelle M. Growth and development of the axr1 mutants of Arabidopsis. Plant Cell. 1990 Nov;2(11):1071–1080. doi: 10.1105/tpc.2.11.1071. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Liu Cm., Xu Zh., Chua N. H. Auxin Polar Transport Is Essential for the Establishment of Bilateral Symmetry during Early Plant Embryogenesis. Plant Cell. 1993 Jun;5(6):621–630. doi: 10.1105/tpc.5.6.621. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Long J. A., Moan E. I., Medford J. I., Barton M. K. A member of the KNOTTED class of homeodomain proteins encoded by the STM gene of Arabidopsis. Nature. 1996 Jan 4;379(6560):66–69. doi: 10.1038/379066a0. [DOI] [PubMed] [Google Scholar]
  12. Meinke D. W., Franzmann L. H., Nickle T. C., Yeung E. C. Leafy Cotyledon Mutants of Arabidopsis. Plant Cell. 1994 Aug;6(8):1049–1064. doi: 10.1105/tpc.6.8.1049. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Okada K., Ueda J., Komaki M. K., Bell C. J., Shimura Y. Requirement of the Auxin Polar Transport System in Early Stages of Arabidopsis Floral Bud Formation. Plant Cell. 1991 Jul;3(7):677–684. doi: 10.1105/tpc.3.7.677. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Schneider T., Dinkins R., Robinson K., Shellhammer J., Meinke D. W. An embryo-lethal mutant of Arabidopsis thaliana is a biotin auxotroph. Dev Biol. 1989 Jan;131(1):161–167. doi: 10.1016/s0012-1606(89)80047-8. [DOI] [PubMed] [Google Scholar]
  15. Shevell D. E., Leu W. M., Gillmor C. S., Xia G., Feldmann K. A., Chua N. H. EMB30 is essential for normal cell division, cell expansion, and cell adhesion in Arabidopsis and encodes a protein that has similarity to Sec7. Cell. 1994 Jul 1;77(7):1051–1062. doi: 10.1016/0092-8674(94)90444-8. [DOI] [PubMed] [Google Scholar]
  16. Smyth D. R., Bowman J. L., Meyerowitz E. M. Early flower development in Arabidopsis. Plant Cell. 1990 Aug;2(8):755–767. doi: 10.1105/tpc.2.8.755. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Theologis A. Ethylene sensors: how perceptive! Science. 1995 Dec 15;270(5243):1774–1774. doi: 10.1126/science.270.5243.1774. [DOI] [PubMed] [Google Scholar]
  18. Torres-Ruiz R. A., Jürgens G. Mutations in the FASS gene uncouple pattern formation and morphogenesis in Arabidopsis development. Development. 1994 Oct;120(10):2967–2978. doi: 10.1242/dev.120.10.2967. [DOI] [PubMed] [Google Scholar]
  19. Wilkinson J. Q., Lanahan M. B., Yen H. C., Giovannoni J. J., Klee H. J. An ethylene-inducible component of signal transduction encoded by never-ripe. Science. 1995 Dec 15;270(5243):1807–1809. doi: 10.1126/science.270.5243.1807. [DOI] [PubMed] [Google Scholar]
  20. Wilson A. K., Pickett F. B., Turner J. C., Estelle M. A dominant mutation in Arabidopsis confers resistance to auxin, ethylene and abscisic acid. Mol Gen Genet. 1990 Jul;222(2-3):377–383. doi: 10.1007/BF00633843. [DOI] [PubMed] [Google Scholar]
  21. Yadegari R., Paiva GRd., Laux T., Koltunow A. M., Apuya N., Zimmerman J. L., Fischer R. L., Harada J. J., Goldberg R. B. Cell Differentiation and Morphogenesis Are Uncoupled in Arabidopsis raspberry Embryos. Plant Cell. 1994 Dec;6(12):1713–1729. doi: 10.1105/tpc.6.12.1713. [DOI] [PMC free article] [PubMed] [Google Scholar]

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