Abstract
Two cDNAs isolated from white spruce [Picea glauca (Moench) Voss] somatic embryos, are predicted to encode a basic class IV chitinase and a β-1,3-glucanase, respectively corresponding to genesPgChi-1 andPgGlu-1. Each represents a multigene family in spruce. Transcripts homologous toPgChi-1 orPgGlu-1 genes were highly abundant in embryogenic tissues and gradually decreased after tissues were placed on abscisic acid-containing maturation medium, with lowest abundance in globular embryos. Transcripts related toPgGlu-1 became highly abundant again in early cotyledonary embryos but decreased thereafter, whereas transcripts related toPgChi-1 were also highly abundant in late cotyledonary embryos and plantlets in vitro; transcripts were either low (PgChi-1) or were not detectable (PgGlu-1) in needles. Wounding, drying and flooding stresses enhancedPgChi-1-andPgGlu-1-related gene expression. Fungal cell wall suspension enhancedPgGlu-1-related transcript accumulation, but reducedPgChi-1-related transcript abundance within 24 h.PgChi-1 andPgGlu-1 and their homologues may have roles in plant defense, and possibly developmental roles during spruce somatic embryo maturation.
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Abbreviations
- PR:
-
pathogenesis related
References
Ayers AR, Ebel J, Valent B, Albersheim P (1976) Host-pathogen interactions. X. Fraction and biological activity of elicitor isolated from the mycelial walls ofPhytophthora megasperma var.Sojae. Plant Physiol 57: 760–765
Bommineni VR, Chibbar RN, Dalta RSS, Tsang EWT (1993) Transformation of white spruce (Picea glauca) somatic embryos by microprojectile bombardment. Plant Cell Rep 13: 17–23
Bucciaglia PA, Smith AG (1994) Cloning and characterization ofTag1, a β-1,3-glucanase expressed during tetrad dissolution. Plant Mol Biol 24: 903–914
Castresana C, de Carvalho F, Gheysen G, Habets M, Inzé D, van Montagu M (1990) Tissue-specific and pathogen-induced regulation of aNicotiana plumbaginifolia β-1,3-glucanase gene. Plant Cell 2: 1131–1143
Collinge DB, Kragh KM, Mikkelsen JD, Nielsen KK, Rasmussen U, Vad K (1993) Plant Chitinases. Plant J 3: 31–10
de Jong AJ, Cordewener J, Schiavo FL, Terzi M, Vandekerckhove J, van Kammen A, de Vries SC (1992) A carrot somatic embryo mutant is rescued by chitinase. Plant Cell 4: 425–433
de Jong AJ, Heidstra R, Spaink HP, Hartog MV, Meijer EA, Hendriks T, Lo Schiavo F, Terzi M, Bisseling T, van Kammen A, de Vries SC (1993)Rhizobium lipooligosaccharides rescue a carrot somatic embryo mutant. Plant Cell 5: 615–620
de Jong AJ, Hendriks T, Meijer EA, Penning M, Lo Schiavo F, Terzi M, van Kammen A, de Vries SC (1995) Transient reduction in secreted 32 kD chitinase prevents somatic embryogenesis in the carrot (Daucus carota L.) variantts11. Dev Genet 16: 332–343
Domon J-M, Meyer Y, Faye L, David A, David H (1994) Extracellular (glyco)proteins in embryogenic and non-embryogenic cell lines of Caribbean pine. Comparison between phenotypes of Stage one somatic embryos. Plant Physiol Biochem 32:137–147
Dong J-Z, Dunstan DI (1996a) A reliable method for extraction of RNA from various conifer tissues. Plant Cell Rep 15: 516–521
Dong J-Z, Dunstan DI (1996b) Expression of abundant mRNAs during somatic embryogenesis of white spruce [Picea glauca (Moench) Voss]. Planta 199: 469–476
Doyle JJ, Doyle JL, Hortorium LHB (1990) Isolation of plant DNA from fresh tissues. Focus 12: 13–15
Fincher GB (1989) Molecular and cellular biology associated with endosperm mobilization in germinating cereal grains. Annu Rev Plant Physiol Mol Biol 40: 305–346
Hird DL, Worrall D, Hodge R, Smartt S, Paul W, Scott R (1993) The anther-specific protein encoded by theBrassica napus andArabidopsis thaliana A6 gene displays similarity to β-1,3-glucanase. Plant J 4: 1023–1033
Høj PB, Fincher GB (1995) Molecular evolution of plant β-glucan endohydrolases. Plant J 7: 367–379
Høj PB, Hartman DJ, Morrice NA, Doan DNP, Fincher GB (1989) Purification of (1→3)-β-glucan endohydrolase isoenzyme II from germinated barley and determination of its primary structure from a cDNA clone. Plant Mol Biol 13: 31–42
Hon W-C, Griffith M, Mlynarz A, Kwok YC, Yang DSC (1995) Antifreeze proteins in winter rye are similar to pathogenesis-related proteins. Plant Physiol 109: 879–889.
Iseli B, Boller T, Neuhaus J-M (1993) The C-terminal cysteine-rich domain of tobacco class I chitinase is essential for chitin binding but not for catalytic or antifungal activity. Plant Physiol 103: 221–226
Kragh KM, Jacobsen S, Mikkelsen JD, Nielsen KA (1991) Purification and characterization of three chitinases and one β-1,3-glucanase accumulating in the medium of cell suspension cultures of barley (Hordeum vulgare L.). Plant Sci 76: 65–77
Leah R, Tommerup H, Svendsen I, Mundy J (1991) Biochemical and molecular characterization of three barley seed proteins with antifungal properties. J Biol Chem 266: 1564–1573
Linthorst HJM (1991) Pathogenesis-related proteins in plants. Crit Rev Plant Sci 10: 123–150
Lotan T, Ori N, Fluhr R (1989) Pathogenesis-related proteins are developmentally regulated in tobacco flowers. Plant Cell 1: 881–887
Margis-Pinheiro M, Metz-Boutigue MH, Awade A, de Tapia M, le Ret M, Burkard G (1991) Isolation of a complementary DNA encoding the bean PR4 chitinase: an acidic enzyme with an amino-terminus cysteine-rich domain. Plant Mol Biol 17: 243–253
Meeks-Wagner D, Dennis ES, Van KTT, Peacock WJ (1989) Tobacco genes expressed during in vitro floral initiation and their expression during normal plant development. Plant Cell 1: 25–35
Neale AD, Wahleithner JA, Lund M, Bonnett HT, Kelly A, Meeks-Wagner DR, Peacock WJ, Dennis ES (1990) Chitinase, β-1,3-glucanase, osmotin, and extensin are expressed in tobacco explants during flower formation. Plant Cell 2: 673–684
Ohashi Y, Ohshima M (1992) Stress-induced expression of genes for pathogenesis-related proteins in plants. Plant Cell Physiol 33: 819–826
Pellé R, Murphy NB (1993) Northern hybridization: rapid and simple electrophoretic condition. Nucleic Acids Res 21: 2783–2784
Rasmussen U, Bojsen K, Collinge DB (1992) Cloning and characterization of a pathogen-induced chitinase inBrassica napus. Plant Mol Biol 20: 277–287
Sharon N, Lis H (1979) Comparative biochemistry of plant glycoproteins. Biochem Rev 7: 783–799
Shinshi H, Mohnen D, Meins Jr. F (1987) Regulation of a plant pathogenesis-related enzyme: inhibition of chitinase and chitinase mRNA accumulation in cultured tobacco tissues by auxin and cytokinin. Proc Natl Acad Sci USA 84: 89–93
Singh H, Owens JH (1981) Sexual reproduction of Engelmann spruce (Picea engelmannii). Can J Bot 59: 793–810
Tinline RD, Srauffer JF, Dickson JG (1960)Cochliobolus sativus III. Effects of ultraviolet irradiation. Can J Bot 38: 275–282
von Arnold S, Egertsdotter U, Mo LH (1995) Importance of extracellular proteins for somatic embryogenesis inPicea abies. In: Terzi M, Cella R, Falavigna A (eds) Current Issues in plant molecular and cellular biology. Kluwer Academic Publishers, Dordrecht, Netherlands, pp 389–392
von Heijne G (1983) Patterns of amino acids near signal-sequence cleavage sites. Eur J Biochem 133: 17–21
Ward ER, Payne GB, Moyer MB, Williams SC, Dincher SS, Sharkey KC, Beck JJ, Taylor HT, Ahl-Goy P, Meins Jr. F Ryals JA (1991) Differential regulation of beta-1,3-glucanase messenger RNAs in response to pathogen infection. Plant Physiol 96: 390–397
Wu S, Kriz AL, Widholm JM, 1994. Nucleotide sequence of a maize cDNA for a class II, acidic β-1,3-glucanase. Plant Physiol 106: 1709–1710
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Nucleotide sequences appear in the GenBank Nucleotide Sequence Databases under the accession numbers L42467 (PgChi-1) and L49179 (PgGlu-1)
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Dong, JZ., Dunstan, D.I. Endochitinase and β-1,3-glucanase genes are developmentally regulated during somatic embryogenesis inPicea glauca . Planta 201, 189–194 (1997). https://doi.org/10.1007/BF01007703
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DOI: https://doi.org/10.1007/BF01007703