Abstract
We have isolated and characterized cDNA clones of a gene family (P2) expressed in Oenothera organensis pollen. This family contains approximately six to eight family members and is expressed at high levels only in pollen. The predicted protein sequence from a near full-length cDNA clone shows that the protein products of these genes are at least 38,000 daltons. We identified the protein encoded by one of the cDNAs in this family by using antibodies to beta-galactosidase/pollen cDNA fusion proteins. Immunoblot analysis using these antibodies identifies a family of proteins of approximately 40 kilodaltons that is present in mature pollen, indicating that these mRNAs are not stored solely for translation after pollen germination. These proteins accumulate late in pollen development and are not detectable in other parts of the plant. Although not present in unpollinated or self-pollinated styles, the 40-kilodalton to 45-kilodalton antigens are detectable in extracts from cross-pollinated styles, suggesting that the proteins are present in pollen tubes growing through the style during pollination. The proteins are also present in pollen tubes growing in vitro. Both nucleotide and amino acid sequences are similar to the published sequences for cDNAs encoding the enzyme polygalacturonase, which suggests that the P2 gene family may function in depolymerizing pectin during pollen development, germination, and tube growth. Cross-hybridizing RNAs and immunoreactive proteins were detected in pollen from a wide variety of plant species, which indicates that the P2 family of polygalacturonase-like genes are conserved and may be expressed in the pollen from many angiosperms.
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- Dellapenna D., Alexander D. C., Bennett A. B. Molecular cloning of tomato fruit polygalacturonase: Analysis of polygalacturonase mRNA levels during ripening. Proc Natl Acad Sci U S A. 1986 Sep;83(17):6420–6424. doi: 10.1073/pnas.83.17.6420. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Emerson S. The Genetics of Self-Incompatibility in Oenothera Organensis. Genetics. 1938 Mar;23(2):190–202. doi: 10.1093/genetics/23.2.190. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Finkelstein R. R., Tenbarge K. M., Shumway J. E., Crouch M. L. Role of ABA in Maturation of Rapeseed Embryos. Plant Physiol. 1985 Jul;78(3):630–636. doi: 10.1104/pp.78.3.630. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Freeling M. Intragenic recombination in maize: pollen analysis methods and the effect of parental adh1 isoalleles. Genetics. 1976 Aug;83(4):701–717. doi: 10.1093/genetics/83.4.701. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gasser C. S., Budelier K. A., Smith A. G., Shah D. M., Fraley R. T. Isolation of Tissue-Specific cDNAs from Tomato Pistils. Plant Cell. 1989 Jan;1(1):15–24. doi: 10.1105/tpc.1.1.15. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Giovannoni J. J., DellaPenna D., Bennett A. B., Fischer R. L. Expression of a chimeric polygalacturonase gene in transgenic rin (ripening inhibitor) tomato fruit results in polyuronide degradation but not fruit softening. Plant Cell. 1989 Jan;1(1):53–63. doi: 10.1105/tpc.1.1.53. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Guo L. H., Stepień P. P., Tso J. Y., Brousseau R., Narang S., Thomas D. Y., Wu R. Synthesis of human insulin gene. VIII. Construction of expression vectors for fused proinsulin production in Escherichia coli. Gene. 1984 Jul-Aug;29(1-2):251–254. doi: 10.1016/0378-1119(84)90186-0. [DOI] [PubMed] [Google Scholar]
- Hodgson C. P., Fisk R. Z. Hybridization probe size control: optimized 'oligolabelling'. Nucleic Acids Res. 1987 Aug 11;15(15):6295–6295. doi: 10.1093/nar/15.15.6295. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Joshi C. P. Putative polyadenylation signals in nuclear genes of higher plants: a compilation and analysis. Nucleic Acids Res. 1987 Dec 10;15(23):9627–9640. doi: 10.1093/nar/15.23.9627. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mascarenhas J. P., Bell E. RNA synthesis during development of the male gametophyte of Tradescantia. Dev Biol. 1970 Apr;21(4):475–490. doi: 10.1016/0012-1606(70)90073-4. [DOI] [PubMed] [Google Scholar]
- Sachs M. M., Dennis E. S., Gerlach W. L., Peacock W. J. Two Alleles of Maize ALCOHOL DEHYDROGENASE 1 Have 3' Structural and Poly(a) Addition Polymorphisms. Genetics. 1986 Jun;113(2):449–467. doi: 10.1093/genetics/113.2.449. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Scofield S. R., Crouch M. L. Nucleotide sequence of a member of the napin storage protein family from Brassica napus. J Biol Chem. 1987 Sep 5;262(25):12202–12208. [PubMed] [Google Scholar]
- Steffensen D. M. Synthesis of ribosomal RNA during growth and division in Lilium. Exp Cell Res. 1966 Oct;44(1):1–12. doi: 10.1016/0014-4827(66)90407-1. [DOI] [PubMed] [Google Scholar]
- Stinson J. R., Eisenberg A. J., Willing R. P., Pe M. E., Hanson D. D., Mascarenhas J. P. Genes expressed in the male gametophyte of flowering plants and their isolation. Plant Physiol. 1987 Feb;83(2):442–447. doi: 10.1104/pp.83.2.442. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tanksley S. D., Zamir D., Rick C. M. Evidence for Extensive Overlap of Sporophytic and Gametophytic Gene Expression in Lycopersicon esculentum. Science. 1981 Jul 24;213(4506):453–455. doi: 10.1126/science.213.4506.453. [DOI] [PubMed] [Google Scholar]
- Ursin V. M., Yamaguchi J., McCormick S. Gametophytic and sporophytic expression of anther-specific genes in developing tomato anthers. Plant Cell. 1989 Jul;1(7):727–736. doi: 10.1105/tpc.1.7.727. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Willing R. P., Mascarenhas J. P. Analysis of the Complexity and Diversity of mRNAs from Pollen and Shoots of Tradescantia. Plant Physiol. 1984 Jul;75(3):865–868. doi: 10.1104/pp.75.3.865. [DOI] [PMC free article] [PubMed] [Google Scholar]