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. 1989 Nov;1(11):1095–1109. doi: 10.1105/tpc.1.11.1095

Soybean Seed Protein Genes Are Regulated Spatially during Embryogenesis.

L Perez-Grau 1, R B Goldberg 1
PMCID: PMC159846  PMID: 12359887

Abstract

We used in situ hybridization to investigate Kunitz trypsin inhibitor gene expression programs at the cell level in soybean embryos and in transformed tobacco seeds. The major Kunitz trypsin inhibitor mRNA, designated as KTi3, is first detectable in a specific globular stage embryo region, and then becomes localized within the axis of heart, cotyledon, and maturation stage embryos. By contrast, a related Kunitz trypsin inhibitor mRNA class, designated as KTi1/2, is not detectable during early embryogenesis. Nor is the KTi1/2 mRNA detectable in the axis at later developmental stages. Outer perimeter cells of each cotyledon accumulate both KTi1/2 and KTi3 mRNAs early in maturation. These mRNAs accumulate progressively from the outside to inside of each cotyledon in a "wave-like" pattern as embryogenesis proceeds. A similar KTi3 mRNA localization pattern is observed in soybean somatic embryos and in transformed tobacco seeds. An unrelated mRNA, encoding [beta]-conglycinin storage protein, also accumulates in a wave-like pattern during soybean embryogenesis. Our results indicate that cell-specific differences in seed protein gene expression programs are established early in development, and that seed protein mRNAs accumulate in a precise cellular pattern during seed maturation. We also show that seed protein gene expression patterns are conserved at the cell level in embryos of distantly related plants, and that these patterns are established in the absence of non-embryonic tissues.

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Selected References

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

  1. Allen R. D., Bernier F., Lessard P. A., Beachy R. N. Nuclear factors interact with a soybean beta-conglycinin enhancer. Plant Cell. 1989 Jun;1(6):623–631. doi: 10.1105/tpc.1.6.623. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Barker S. J., Harada J. J., Goldberg R. B. Cellular localization of soybean storage protein mRNA in transformed tobacco seeds. Proc Natl Acad Sci U S A. 1988 Jan;85(2):458–462. doi: 10.1073/pnas.85.2.458. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bustos M. M., Guiltinan M. J., Jordano J., Begum D., Kalkan F. A., Hall T. C. Regulation of beta-glucuronidase expression in transgenic tobacco plants by an A/T-rich, cis-acting sequence found upstream of a French bean beta-phaseolin gene. Plant Cell. 1989 Sep;1(9):839–853. doi: 10.1105/tpc.1.9.839. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Chen Z. L., Naito S., Nakamura I., Beachy R. N. Regulated expression of genes encoding soybean beta-conglycinins in transgenic plants. Dev Genet. 1989;10(2):112–122. doi: 10.1002/dvg.1020100207. [DOI] [PubMed] [Google Scholar]
  5. Chen Z. L., Pan N. S., Beachy R. N. A DNA sequence element that confers seed-specific enhancement to a constitutive promoter. EMBO J. 1988 Feb;7(2):297–302. doi: 10.1002/j.1460-2075.1988.tb02812.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Chen Z. L., Schuler M. A., Beachy R. N. Functional analysis of regulatory elements in a plant embryo-specific gene. Proc Natl Acad Sci U S A. 1986 Nov;83(22):8560–8564. doi: 10.1073/pnas.83.22.8560. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Christianson M. L., Warnick D. A., Carlson P. S. A morphogenetically competent soybean suspension culture. Science. 1983 Nov 11;222(4624):632–634. doi: 10.1126/science.222.4624.632. [DOI] [PubMed] [Google Scholar]
  8. Davidson E. H. Lineage-specific gene expression and the regulative capacities of the sea urchin embryo: a proposed mechanism. Development. 1989 Mar;105(3):421–445. doi: 10.1242/dev.105.3.421. [DOI] [PubMed] [Google Scholar]
  9. Goldberg R. B., Hoschek G., Ditta G. S., Breidenbach R. W. Developmental regulation of cloned superabundant embryo mRNAs in soybean. Dev Biol. 1981 Apr 30;83(2):218–231. doi: 10.1016/0012-1606(81)90468-1. [DOI] [PubMed] [Google Scholar]
  10. Harada J. J., Barker S. J., Goldberg R. B. Soybean beta-conglycinin genes are clustered in several DNA regions and are regulated by transcriptional and posttranscriptional processes. Plant Cell. 1989 Apr;1(4):415–425. doi: 10.1105/tpc.1.4.415. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Jofuku K. D., Goldberg R. B. Kunitz trypsin inhibitor genes are differentially expressed during the soybean life cycle and in transformed tobacco plants. Plant Cell. 1989 Nov;1(11):1079–1093. doi: 10.1105/tpc.1.11.1079. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Jofuku K. D., Okamuro J. K., Goldberg R. B. Interaction of an embryo DNA binding protein with a soybean lectin gene upstream region. Nature. 1987 Aug 20;328(6132):734–737. doi: 10.1038/328734a0. [DOI] [PubMed] [Google Scholar]
  13. Jofuku K. D., Schipper R. D., Goldberg R. B. A frameshift mutation prevents Kunitz trypsin inhibitor mRNA accumulation in soybean embryos. Plant Cell. 1989 Apr;1(4):427–435. doi: 10.1105/tpc.1.4.427. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Walling L., Drews G. N., Goldberg R. B. Transcriptional and post-transcriptional regulation of soybean seed protein mRNA levels. Proc Natl Acad Sci U S A. 1986 Apr;83(7):2123–2127. doi: 10.1073/pnas.83.7.2123. [DOI] [PMC free article] [PubMed] [Google Scholar]

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