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The Role of the Maize Viviparous-1 Gene in Regulation of Seed Maturation

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Cellular Communication in Plants

Abstract

Late in the course of seed formation tissues that are destined to remain viable in the dry seed undergo a maturation process during which further development is arrested and tolerance to desiccation is acquired. The viviparous mutants of maize which fail to complete maturation identify genes that are essential for this process (Robertson, 1955; McCarty and Carson, 1991; McCarty et al., 1992). In this paper we will address the regulation of the maturation program on two levels: 1) how intrinsic and extrinsic signals are integrated to produce a developmentally specific response and 2) how the diverse metabolic pathways associated with maturation are integrated by a regulatory hierarchy into a common developmental program. We explore the notion that these two integration processes are intimately related and involve a common mechanism operating at the level of transcriptional regulation. This model is motivated by our analysis of the role of the Viviparous-1 (Vp1) gene in regulating the maturation program in maize. Finally, our results offer some insight into how at least part of the regulatory network controlling maturation evolved.

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References

  • Armstrong, G. A., Weishaar, B. and Hahlbrock, K. 1992. Hommodimeric and hetero-dimeric leucine zipper proteins and nuclear factors from parsley recognize diverse promoter elements with ACGT cores. Plant Cell. 4:525–537.

    PubMed  CAS  Google Scholar 

  • Chen, S. M. and E. H. Coe, Jr. 1978. Control of anthocyanin synthesis by the C locus in maize. Biochem. Genet. 15: 333–346.

    Article  Google Scholar 

  • Coe, E. H. and M. G. Neuffer. 1977. The genetics of corn. In Corn and corn improvement. (G. F. Sprague, ed). pp. 111–213. American Society of Agronomy, Madison, WI.

    Google Scholar 

  • Cone, K. C., F. A. Burr and B. Burr. 1986. Molecular analysis of the maize anthocyanin regulatory locus ci. Proc. Nat. Acad. Sci. USA. 83:9631–9635.

    Article  PubMed  CAS  Google Scholar 

  • DeLisle, A. and Ferl, R. J. 1990. Characterization of the Arabidopsis Adh G-box binding factor. Plant Cell. 2:547–557.

    PubMed  CAS  Google Scholar 

  • Dooner, H. K. 1985. Viviparous-1 mutation in maize conditions pleiotropic enzyme deficiencies in the aleurone. Plant Physiol. 77:486–488.

    Article  PubMed  CAS  Google Scholar 

  • Dickinson, C. D., R. P. Evans and Niels C. Neilsen. 1988. RY repeats are conserved in the 5’-flanking regions of legume seed-protein genes. Nucleic Acids Res. 16: 371.

    Article  PubMed  CAS  Google Scholar 

  • Goff, S., K. C. Cone and M. E. Fromm. 1991. Identification of functional domains in the maize transcriptional activator C1: comparison of wild-type and dominant inhibitor proteins. Genes and Dev. 5:298–309.

    Article  PubMed  CAS  Google Scholar 

  • Goff, S., T. M. Klein, B. A. Roth, M. E. Fromm, K. C. Cone, J. P. Radicella and V. L. Chandler. 1990. Transactivation of anthocyanin biosynthetic genes following transfer of B regulatory genes into maize tissues. EMBO J. 9:2517–2522.

    PubMed  CAS  Google Scholar 

  • Gomez, J., Sanchez-Martinez, D., Stiefel, V., Rigau, J., Puigdomenech and Pages, M. 1988. A gene induced by the plant hormone abscisic acid in response to water stress encodes a glycine-rich protein. Nature. 334:262–264.

    Article  PubMed  CAS  Google Scholar 

  • Guiltinan, M. J., W. R. Marcotte, R. S. Quatrano. 1990. A leucine zipper protein that recognizes an abscisic acid response element. Science 250:267–270.

    Article  PubMed  CAS  Google Scholar 

  • Hattori, T., Vasil, V., Rosenkrans, L., Hannah, L. C, McCarty, D. R. and Vasil, I. K. 1992. The Viviparous-1 gene and abscisic acid activate the C1 regulatory gene for anthocyanin biosynthesis during seed maturation in maize. Gen. Dev. 6:609–618.

    Article  CAS  Google Scholar 

  • Ludwig, S. R., L. F. Habera, S. L. Delaporta and S. R. Wessler. 1989. Lc, a member of the maize R gene family responsible for tissue-specific anthocyanin production, encodes protein similar to transcriptional activators and contains the myc-homology region. Proc. Natl. Acad. Sci. USA 86:7092–7096.

    Article  PubMed  CAS  Google Scholar 

  • Marcotte, W. R. Jr., C. C. Bayley and R. S. Quatrano. 1988. Regulation of a wheat promoter by abscisic acid in rice protoplasts. Nature 335:454–457.

    Article  CAS  Google Scholar 

  • Marcotte, W. R. Jr., S. H. Russell and R. S. Quatrano. 1989. Abscisic acid response sequences from the Em gene of wheat. Plant Cell 1:969–976.

    PubMed  CAS  Google Scholar 

  • McCarty, D. R. 1992. The role of VP1 in regulation of seed maturation in maize. Bio-chem. Soc. Trans. 20:89–92.

    CAS  Google Scholar 

  • McCarty, D. R., C. B. Carson, M. Lazar and S. C. Simonds. 1989a. Transposable element induced mutations of the viviparous-1 gene of maize. Dev. Genetics. 10: 473–481.

    Article  CAS  Google Scholar 

  • McCarty, D. R., C. B. Carson, P. S. Stinard and D. S. Robertson. 1989b. Molecular analysis of viviparous-1: An abscisic acid insensitive mutant of maize. Plant Cell 1: 523–532.

    PubMed  CAS  Google Scholar 

  • McCarty, D. R. and C. B. Carson. 1990. The molecular genetics of seed maturation in maize. Physiol Plant. 81: 267–272.

    Article  Google Scholar 

  • McCarty, D. R., T. Hattori, C. B. Carson, V. Vasil and I. K. Vasil. 1991. The viviparous-1 developmental gene of maize encodes a novel transcriptional activator. Cell 66: 895–905.

    Article  PubMed  CAS  Google Scholar 

  • Mundy, J., K. Yamaguchi-Shinozaki and N.-H. Chua. 1990. Nuclear proteins bind conserved elements in the abscisic acid responsive promoter of a rice rab gene. Proc. Nat. Acad. Sci. USA. 87:406–410.

    Article  Google Scholar 

  • Neill, S. J., R. Horgan and A. D. Parry. 1986. The carotenoid and abscisic acid content of viviparous kernels and seedlings of Zea mays L. Planta 169:87–96.

    Article  CAS  Google Scholar 

  • Paz-Ares, J., D. Ghosal, U. Wienand, P. Peterson and H. Saedler. 1987. The regulatory locus c1 of Zea mays encodes a protein with homology to myb proto-oncogene products and with structural similarities to transcriptional activators. EMBO J. 6: 3553–3558.

    PubMed  CAS  Google Scholar 

  • Robertson, D. S. 1955. The genetics of vivipary in maize. Genetics 40: 745–760.

    PubMed  CAS  Google Scholar 

  • Robichaud, C. S., J. Wong and I. M. Sussex. 1980. Control of in vitro growth of viviparous embryo mutants of maize by abscisic acid. Dev. Genetics 1: 325–330.

    Article  CAS  Google Scholar 

  • Robichaud, C. S. and I. M. Sussex. 1986. The response of viviparous-1 and wildtype embryos of Zea mays to culture in the presence of abscisic acid. J. Plant Physiol. 126: 235–242.

    Article  CAS  Google Scholar 

  • Robichaud, C. S. and I. M. Sussex. 1987. The uptake and metabolism of 14C-ABA by excised wild type and viviparous-1 embryos of Zea mays L. J. Plant Physiol. 130: 181–188.

    Article  CAS  Google Scholar 

  • Roth, B. A., S. A. Goff, T. M. Klein and M. E. Fromm. 1991. C1 and R1 dependent expression of the maize Bz1 gene requires sequences with homology to mammalian myb and myc binding sites. Plant Cell 3:317–325.

    PubMed  CAS  Google Scholar 

  • Senaratna, T., McKersie, B. D. and Bowley, S. R. 1989. Desiccation tolerance of alfalfa (Medicago sativa L.) somatic embryos. Influence of abscisic acid, stress pretreatments and drying rates. Plant Sci. 65:253–259.

    Article  CAS  Google Scholar 

  • Skriver, K. and J. Mundy. 1990. Gene expression in response to abscisic acid and osmotic stress. The Plant Cell 2: 503–512.

    PubMed  CAS  Google Scholar 

  • Vasil, V., M. Clancy, R. J. Ferl, I. K. Vasil and L. C. Hannah. 1989. Increased gene expression by the first intron of the maize sh1 locus in grass species. Plant Physiol. 91:1575–1579.

    Article  PubMed  CAS  Google Scholar 

  • Zack, C. D., R. J. Ferl and L. C. Hannah. 1986. DNA sequence of a shrunken allele of maize evidence for visitation by insertional sequences. Maydica 31:5–16.

    CAS  Google Scholar 

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McCarty, D.R. (1993). The Role of the Maize Viviparous-1 Gene in Regulation of Seed Maturation. In: Amasino, R.M. (eds) Cellular Communication in Plants. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-9607-0_5

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  • DOI: https://doi.org/10.1007/978-1-4757-9607-0_5

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4757-9609-4

  • Online ISBN: 978-1-4757-9607-0

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