Skip to main content
The Plant Cell logoLink to The Plant Cell
. 1995 Feb;7(2):225–234. doi: 10.1105/tpc.7.2.225

NFL, the tobacco homolog of FLORICAULA and LEAFY, is transcriptionally expressed in both vegetative and floral meristems.

A J Kelly 1, M B Bonnlander 1, D R Meeks-Wagner 1
PMCID: PMC160778  PMID: 7756832

Abstract

The homologous genes FLORICAULA (FLO) of Antirrhinum and LEAFY (LFY) of Arabidopsis regulate the formation of determinate floral meristems. Transcripts of these single-copy genes are confined to floral meristems and some floral organs as well as to the leaflike bracts that subtend Antirrhinum flowers. Based on these observations, we hypothesized that the transcription of genes homologous to FLO and LFY in tobacco, a determinate plant in which the primary shoot apex is consumed in the production of a terminal flower, would serve as a molecular marker for floral commitment. Surprisingly, transcripts of the tobacco homologs NFL1 and NFL2 (Nicotiana FLO/LFY) were found not only in floral meristems, but also in indeterminate vegetative meristems. This implies that the transcriptional expression of the FLO/LFY homologous genes in the apical meristem is not sufficient for the initiation of floral meristem development. In addition, the transcript patterns of the NFL genes identified a previously undescribed subset of cells within the shoot apical meristem that may indicate unique functional compartmentalization. This suggests that, unlike FLO and LFY, which specify determinacy only during floral development, the NFL genes act to specify determinacy in the progenitor cells for both flowers and leaves.

Full Text

The Full Text of this article is available as a PDF (2.5 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Boutry M., Chua N. H. A nuclear gene encoding the beta subunit of the mitochondrial ATP synthase in Nicotiana plumbaginifolia. EMBO J. 1985 Sep;4(9):2159–2165. doi: 10.1002/j.1460-2075.1985.tb03910.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bowman J. L., Smyth D. R., Meyerowitz E. M. Genes directing flower development in Arabidopsis. Plant Cell. 1989 Jan;1(1):37–52. doi: 10.1105/tpc.1.1.37. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bradley D., Carpenter R., Sommer H., Hartley N., Coen E. Complementary floral homeotic phenotypes result from opposite orientations of a transposon at the plena locus of Antirrhinum. Cell. 1993 Jan 15;72(1):85–95. doi: 10.1016/0092-8674(93)90052-r. [DOI] [PubMed] [Google Scholar]
  4. Coen E. S., Meyerowitz E. M. The war of the whorls: genetic interactions controlling flower development. Nature. 1991 Sep 5;353(6339):31–37. doi: 10.1038/353031a0. [DOI] [PubMed] [Google Scholar]
  5. Coen E. S., Romero J. M., Doyle S., Elliott R., Murphy G., Carpenter R. floricaula: a homeotic gene required for flower development in antirrhinum majus. Cell. 1990 Dec 21;63(6):1311–1322. doi: 10.1016/0092-8674(90)90426-f. [DOI] [PubMed] [Google Scholar]
  6. Devereux J., Haeberli P., Smithies O. A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Res. 1984 Jan 11;12(1 Pt 1):387–395. doi: 10.1093/nar/12.1part1.387. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Drews G. N., Bowman J. L., Meyerowitz E. M. Negative regulation of the Arabidopsis homeotic gene AGAMOUS by the APETALA2 product. Cell. 1991 Jun 14;65(6):991–1002. doi: 10.1016/0092-8674(91)90551-9. [DOI] [PubMed] [Google Scholar]
  8. Fitzgerald K., Wilkinson H. A., Greenwald I. glp-1 can substitute for lin-12 in specifying cell fate decisions in Caenorhabditis elegans. Development. 1993 Dec;119(4):1019–1027. doi: 10.1242/dev.119.4.1019. [DOI] [PubMed] [Google Scholar]
  9. Fleming A. J., Mandel T., Roth I., Kuhlemeier C. The patterns of gene expression in the tomato shoot apical meristem. Plant Cell. 1993 Mar;5(3):297–309. doi: 10.1105/tpc.5.3.297. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Goldschmidt R. SOME ASPECTS OF EVOLUTION. Science. 1933 Dec 15;78(2033):539–547. doi: 10.1126/science.78.2033.539. [DOI] [PubMed] [Google Scholar]
  11. Huijser P., Klein J., Lönnig W. E., Meijer H., Saedler H., Sommer H. Bracteomania, an inflorescence anomaly, is caused by the loss of function of the MADS-box gene squamosa in Antirrhinum majus. EMBO J. 1992 Apr;11(4):1239–1249. doi: 10.1002/j.1460-2075.1992.tb05168.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Irish V. F., Sussex I. M. Function of the apetala-1 gene during Arabidopsis floral development. Plant Cell. 1990 Aug;2(8):741–753. doi: 10.1105/tpc.2.8.741. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Jack T., Brockman L. L., Meyerowitz E. M. The homeotic gene APETALA3 of Arabidopsis thaliana encodes a MADS box and is expressed in petals and stamens. Cell. 1992 Feb 21;68(4):683–697. doi: 10.1016/0092-8674(92)90144-2. [DOI] [PubMed] [Google Scholar]
  14. Jacob F. Evolution and tinkering. Science. 1977 Jun 10;196(4295):1161–1166. doi: 10.1126/science.860134. [DOI] [PubMed] [Google Scholar]
  15. Kelly A. J., Zagotta M. T., White R. A., Chang C., Meeks-Wagner D. R. Identification of genes expressed in the tobacco shoot apex during the floral transition. Plant Cell. 1990 Oct;2(10):963–972. doi: 10.1105/tpc.2.10.963. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Kempin S. A., Mandel M. A., Yanofsky M. F. Conversion of perianth into reproductive organs by ectopic expression of the tobacco floral homeotic gene NAG1. Plant Physiol. 1993 Dec;103(4):1041–1046. doi: 10.1104/pp.103.4.1041. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. King M. C., Wilson A. C. Evolution at two levels in humans and chimpanzees. Science. 1975 Apr 11;188(4184):107–116. doi: 10.1126/science.1090005. [DOI] [PubMed] [Google Scholar]
  18. Koltunow A. M., Truettner J., Cox K. H., Wallroth M., Goldberg R. B. Different Temporal and Spatial Gene Expression Patterns Occur during Anther Development. Plant Cell. 1990 Dec;2(12):1201–1224. doi: 10.1105/tpc.2.12.1201. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Li X., Noll M. Evolution of distinct developmental functions of three Drosophila genes by acquisition of different cis-regulatory regions. Nature. 1994 Jan 6;367(6458):83–87. doi: 10.1038/367083a0. [DOI] [PubMed] [Google Scholar]
  20. Mandel M. A., Gustafson-Brown C., Savidge B., Yanofsky M. F. Molecular characterization of the Arabidopsis floral homeotic gene APETALA1. Nature. 1992 Nov 19;360(6401):273–277. doi: 10.1038/360273a0. [DOI] [PubMed] [Google Scholar]
  21. Medford J. I., Elmer J. S., Klee H. J. Molecular cloning and characterization of genes expressed in shoot apical meristems. Plant Cell. 1991 Apr;3(4):359–370. doi: 10.1105/tpc.3.4.359. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Melzer S., Majewski D. M., Apel K. Early Changes in Gene Expression during the Transition from Vegetative to Generative Growth in the Long-Day Plant Sinapis alba. Plant Cell. 1990 Oct;2(10):953–961. doi: 10.1105/tpc.2.10.953. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Okamuro J. K., den Boer B. G., Jofuku K. D. Regulation of Arabidopsis flower development. Plant Cell. 1993 Oct;5(10):1183–1193. doi: 10.1105/tpc.5.10.1183. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Patel N. H. Developmental evolution: insights from studies of insect segmentation. Science. 1994 Oct 28;266(5185):581–590. doi: 10.1126/science.7939712. [DOI] [PubMed] [Google Scholar]
  25. Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Schwarz-Sommer Z., Huijser P., Nacken W., Saedler H., Sommer H. Genetic Control of Flower Development by Homeotic Genes in Antirrhinum majus. Science. 1990 Nov 16;250(4983):931–936. doi: 10.1126/science.250.4983.931. [DOI] [PubMed] [Google Scholar]
  27. Weigel D., Alvarez J., Smyth D. R., Yanofsky M. F., Meyerowitz E. M. LEAFY controls floral meristem identity in Arabidopsis. Cell. 1992 May 29;69(5):843–859. doi: 10.1016/0092-8674(92)90295-n. [DOI] [PubMed] [Google Scholar]
  28. Weigel D., Meyerowitz E. M. Activation of floral homeotic genes in Arabidopsis. Science. 1993 Sep 24;261(5129):1723–1726. doi: 10.1126/science.261.5129.1723. [DOI] [PubMed] [Google Scholar]
  29. Wilson A. C., Maxson L. R., Sarich V. M. Two types of molecular evolution. Evidence from studies of interspecific hybridization. Proc Natl Acad Sci U S A. 1974 Jul;71(7):2843–2847. doi: 10.1073/pnas.71.7.2843. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Wilson A. C., Sarich V. M., Maxson L. R. The importance of gene rearrangement in evolution: evidence from studies on rates of chromosomal, protein, and anatomical evolution. Proc Natl Acad Sci U S A. 1974 Aug;71(8):3028–3030. doi: 10.1073/pnas.71.8.3028. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Yanofsky M. F., Ma H., Bowman J. L., Drews G. N., Feldmann K. A., Meyerowitz E. M. The protein encoded by the Arabidopsis homeotic gene agamous resembles transcription factors. Nature. 1990 Jul 5;346(6279):35–39. doi: 10.1038/346035a0. [DOI] [PubMed] [Google Scholar]
  32. Yasuo H., Satoh N. Function of vertebrate T gene. Nature. 1993 Aug 12;364(6438):582–583. doi: 10.1038/364582b0. [DOI] [PubMed] [Google Scholar]

Articles from The Plant Cell are provided here courtesy of Oxford University Press

RESOURCES