
doi: 10.1007/bf00019486
pmid: 7858212
Brassica napus cv. Topas microspores can be diverted from pollen development toward haploid embryo formation in culture by subjecting them to a heat stress treatment. We show that this switch in developmental pathways is accompanied by the induction of high levels of napin seed storage protein gene expression. Changes in the plant growth or microspore culture conditions were not by themselves sufficient to induce napin gene expression. Specific members of the napin multigene family were cloned from a cDNA library prepared from microspores that had been induced to undergo embryogenesis. The majority of napin clones represented three members (BnmNAP2, BnmNAP3 and BnmNAP4) that, along with a previously isolated napin genomic clone (BngNAP1), constitute the highly conserved BnmNAP subfamily of napin genes. Both RNA gel blot analysis, using a subfamily-specific probe, and histochemical analysis of transgenic plants expressing a BngNAP1 promoter-beta-glucuronidase gene fusion demonstrated that the BnmNAP subfamily is expressed in embryogenic microspores as well as during subsequent stages of microsporic embryo development.
DNA, Complementary, Base Sequence, Recombinant Fusion Proteins, Genetic Vectors, Molecular Sequence Data, Gene Expression, Brassica, Haploidy, Genes, Plant, Germ Cells, Transformation, Genetic, Multigene Family, Sequence Homology, Nucleic Acid, Pollen, Oligonucleotide Probes, Cells, Cultured, 2S Albumins, Plant, Gene Library, Glucuronidase, Plant Proteins
DNA, Complementary, Base Sequence, Recombinant Fusion Proteins, Genetic Vectors, Molecular Sequence Data, Gene Expression, Brassica, Haploidy, Genes, Plant, Germ Cells, Transformation, Genetic, Multigene Family, Sequence Homology, Nucleic Acid, Pollen, Oligonucleotide Probes, Cells, Cultured, 2S Albumins, Plant, Gene Library, Glucuronidase, Plant Proteins
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