Abstract
The ZmHox1a and ZmHox1b (for Zea mays homeobox) genes map on chromosomes 8 and 6, respectively. Both homeobox genes encode proteins that show 91% similarity and are transcribed simultaneously in meristematic and proliferating cells of the maize plant. To gain insight into the biological function of these genes, both open reading frames were expressed in tobacco, under the control of the cauliflower mosaic virus 35S promoter. The resulting transgenic ZmHox1a or ZmHox1b plants showed identical phenotypic alterations that fall into three classes: size reduction, formation of adventitious shoots, and homeotic floral transformations. Approximately 30% of the ZmHox1-expressing plants grew to only one-third of the wild-type size, and most axillary buds gave rise to lateral shoots. Flower abnormalities included formation of petaloid stamens and development of secondary flowers within the primary gynoecium. Therefore, the ectopic expression of the maize ZmHox1 homeobox gene products affects the vegetative as well as the reproductive phase of tobacco plants. All phenotypic alterations were transmitted to the next generation.
Full Text
The Full Text of this article is available as a PDF (2.8 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- A simple and general method for transferring genes into plants. Science. 1985 Mar 8;227(4691):1229–1231. doi: 10.1126/science.227.4691.1229. [DOI] [PubMed] [Google Scholar]
- Becker D., Kemper E., Schell J., Masterson R. New plant binary vectors with selectable markers located proximal to the left T-DNA border. Plant Mol Biol. 1992 Dec;20(6):1195–1197. doi: 10.1007/BF00028908. [DOI] [PubMed] [Google Scholar]
- Bellmann R., Werr W. Zmhox1a, the product of a novel maize homeobox gene, interacts with the Shrunken 26 bp feedback control element. EMBO J. 1992 Sep;11(9):3367–3374. doi: 10.1002/j.1460-2075.1992.tb05415.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Benfey P. N., Chua N. H. The Cauliflower Mosaic Virus 35S Promoter: Combinatorial Regulation of Transcription in Plants. Science. 1990 Nov 16;250(4983):959–966. doi: 10.1126/science.250.4983.959. [DOI] [PubMed] [Google Scholar]
- Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1016/0003-2697(76)90527-3. [DOI] [PubMed] [Google Scholar]
- 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]
- Brandstädter J., Rossbach C., Theres K. The pattern of histone H4 expression in the tomato shoot apex changes during development. Planta. 1994;192(1):69–74. doi: 10.1007/BF00198694. [DOI] [PubMed] [Google Scholar]
- Estruch J. J., Chriqui D., Grossmann K., Schell J., Spena A. The plant oncogene rolC is responsible for the release of cytokinins from glucoside conjugates. EMBO J. 1991 Oct;10(10):2889–2895. doi: 10.1002/j.1460-2075.1991.tb07838.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Estruch J. J., Granell A., Hansen G., Prinsen E., Redig P., Van Onckelen H., Schwarz-Sommer Z., Sommer H., Spena A. Floral development and expression of floral homeotic genes are influenced by cytokinins. Plant J. 1993 Aug;4(2):379–384. doi: 10.1046/j.1365-313x.1993.04020379.x. [DOI] [PubMed] [Google Scholar]
- Estruch J. J., Prinsen E., VAN Onckelen H., Schell J., Spena A. Viviparous leaves produced by somatic activation of an inactive cytokinin-synthesizing gene. Science. 1991 Nov 29;254(5036):1364–1367. doi: 10.1126/science.254.5036.1364. [DOI] [PubMed] [Google Scholar]
- Gallie D. R., Lucas W. J., Walbot V. Visualizing mRNA expression in plant protoplasts: factors influencing efficient mRNA uptake and translation. Plant Cell. 1989 Mar;1(3):301–311. doi: 10.1105/tpc.1.3.301. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gallie D. R., Sleat D. E., Watts J. W., Turner P. C., Wilson T. M. The 5'-leader sequence of tobacco mosaic virus RNA enhances the expression of foreign gene transcripts in vitro and in vivo. Nucleic Acids Res. 1987 Apr 24;15(8):3257–3273. doi: 10.1093/nar/15.8.3257. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Grueneberg D. A., Natesan S., Alexandre C., Gilman M. Z. Human and Drosophila homeodomain proteins that enhance the DNA-binding activity of serum response factor. Science. 1992 Aug 21;257(5073):1089–1095. doi: 10.1126/science.257.5073.1089. [DOI] [PubMed] [Google Scholar]
- Helentjaris T., Weber D., Wright S. Identification of the genomic locations of duplicate nucleotide sequences in maize by analysis of restriction fragment length polymorphisms. Genetics. 1988 Feb;118(2):353–363. doi: 10.1093/genetics/118.2.353. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jofuku K. D., den Boer B. G., Van Montagu M., Okamuro J. K. Control of Arabidopsis flower and seed development by the homeotic gene APETALA2. Plant Cell. 1994 Sep;6(9):1211–1225. doi: 10.1105/tpc.6.9.1211. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kempin S. A., Savidge B., Yanofsky M. F. Molecular basis of the cauliflower phenotype in Arabidopsis. Science. 1995 Jan 27;267(5197):522–525. doi: 10.1126/science.7824951. [DOI] [PubMed] [Google Scholar]
- Larkin J. C., Oppenheimer D. G., Lloyd A. M., Paparozzi E. T., Marks M. D. Roles of the GLABROUS1 and TRANSPARENT TESTA GLABRA Genes in Arabidopsis Trichome Development. Plant Cell. 1994 Aug;6(8):1065–1076. doi: 10.1105/tpc.6.8.1065. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Maas C., Schaal S., Werr W. A feedback control element near the transcription start site of the maize Shrunken gene determines promoter activity. EMBO J. 1990 Nov;9(11):3447–3452. doi: 10.1002/j.1460-2075.1990.tb07552.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Medford J. I., Horgan R., El-Sawi Z., Klee H. J. Alterations of Endogenous Cytokinins in Transgenic Plants Using a Chimeric Isopentenyl Transferase Gene. Plant Cell. 1989 Apr;1(4):403–413. doi: 10.1105/tpc.1.4.403. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mizukami Y., Ma H. Ectopic expression of the floral homeotic gene AGAMOUS in transgenic Arabidopsis plants alters floral organ identity. Cell. 1992 Oct 2;71(1):119–131. doi: 10.1016/0092-8674(92)90271-d. [DOI] [PubMed] [Google Scholar]
- Nelson D., Salamini F., Bartels D. Abscisic acid promotes novel DNA-binding activity to a desiccation-related promoter of Craterostigma plantagineum. Plant J. 1994 Apr;5(4):451–458. doi: 10.1046/j.1365-313x.1994.5040451.x. [DOI] [PubMed] [Google Scholar]
- Poethig R. S. Phase change and the regulation of shoot morphogenesis in plants. Science. 1990 Nov 16;250(4983):923–930. doi: 10.1126/science.250.4983.923. [DOI] [PubMed] [Google Scholar]
- Ray A., Robinson-Beers K., Ray S., Baker S. C., Lang J. D., Preuss D., Milligan S. B., Gasser C. S. Arabidopsis floral homeotic gene BELL (BEL1) controls ovule development through negative regulation of AGAMOUS gene (AG). Proc Natl Acad Sci U S A. 1994 Jun 21;91(13):5761–5765. doi: 10.1073/pnas.91.13.5761. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rerie W. G., Feldmann K. A., Marks M. D. The GLABRA2 gene encodes a homeo domain protein required for normal trichome development in Arabidopsis. Genes Dev. 1994 Jun 15;8(12):1388–1399. doi: 10.1101/gad.8.12.1388. [DOI] [PubMed] [Google Scholar]
- Romano C. P., Hein M. B., Klee H. J. Inactivation of auxin in tobacco transformed with the indoleacetic acid-lysine synthetase gene of Pseudomonas savastanoi. Genes Dev. 1991 Mar;5(3):438–446. doi: 10.1101/gad.5.3.438. [DOI] [PubMed] [Google Scholar]
- Ruberti I., Sessa G., Lucchetti S., Morelli G. A novel class of plant proteins containing a homeodomain with a closely linked leucine zipper motif. EMBO J. 1991 Jul;10(7):1787–1791. doi: 10.1002/j.1460-2075.1991.tb07703.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Saghai-Maroof M. A., Soliman K. M., Jorgensen R. A., Allard R. W. Ribosomal DNA spacer-length polymorphisms in barley: mendelian inheritance, chromosomal location, and population dynamics. Proc Natl Acad Sci U S A. 1984 Dec;81(24):8014–8018. doi: 10.1073/pnas.81.24.8014. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schena M., Davis R. W. HD-Zip proteins: members of an Arabidopsis homeodomain protein superfamily. Proc Natl Acad Sci U S A. 1992 May 1;89(9):3894–3898. doi: 10.1073/pnas.89.9.3894. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schindler U., Beckmann H., Cashmore A. R. HAT3.1, a novel Arabidopsis homeodomain protein containing a conserved cysteine-rich region. Plant J. 1993 Jul;4(1):137–150. doi: 10.1046/j.1365-313x.1993.04010137.x. [DOI] [PubMed] [Google Scholar]
- 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]
- Scott M. P., Tamkun J. W., Hartzell G. W., 3rd The structure and function of the homeodomain. Biochim Biophys Acta. 1989 Jul 28;989(1):25–48. doi: 10.1016/0304-419x(89)90033-4. [DOI] [PubMed] [Google Scholar]
- Sinha N. R., Williams R. E., Hake S. Overexpression of the maize homeo box gene, KNOTTED-1, causes a switch from determinate to indeterminate cell fates. Genes Dev. 1993 May;7(5):787–795. doi: 10.1101/gad.7.5.787. [DOI] [PubMed] [Google Scholar]
- Thomas J. H. Thinking about genetic redundancy. Trends Genet. 1993 Nov;9(11):395–399. doi: 10.1016/0168-9525(93)90140-d. [DOI] [PubMed] [Google Scholar]
- Töpfer R., Matzeit V., Gronenborn B., Schell J., Steinbiss H. H. A set of plant expression vectors for transcriptional and translational fusions. Nucleic Acids Res. 1987 Jul 24;15(14):5890–5890. doi: 10.1093/nar/15.14.5890. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vollbrecht E., Veit B., Sinha N., Hake S. The developmental gene Knotted-1 is a member of a maize homeobox gene family. Nature. 1991 Mar 21;350(6315):241–243. doi: 10.1038/350241a0. [DOI] [PubMed] [Google Scholar]
- Weigel D., Meyerowitz E. M. The ABCs of floral homeotic genes. Cell. 1994 Jul 29;78(2):203–209. doi: 10.1016/0092-8674(94)90291-7. [DOI] [PubMed] [Google Scholar]
- van der Krol A. R., Brunelle A., Tsuchimoto S., Chua N. H. Functional analysis of petunia floral homeotic MADS box gene pMADS1. Genes Dev. 1993 Jul;7(7A):1214–1228. doi: 10.1101/gad.7.7a.1214. [DOI] [PubMed] [Google Scholar]
