Plant Physiology

Blum, A.; Munns, R.; Passioura, J. B.; Turner, N. C.; Sharp, R. E.; Boyer, J. S.; Nguyen, H. T.; Hsiao, T. C.; Verma, DPS.; Hong, Z.

doi: 10.1104/pp.110.4.1051pmid: 12226240

Article PDF first page preview Close This content is only available as a PDF. Copyright © 1996 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

Huang, AHC.

doi: 10.1104/pp.110.4.1055pmid: 8934621

Article PDF first page preview Close This content is only available as a PDF. Copyright © 1996 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

Henriksen, G. H.; Taylor, A. R.; Brownlee, C.; Assmann, S. M.

doi: 10.1104/pp.110.4.1063pmid: 11541144

Abstract Plasma membranes of guard cells in epidermal peels of Vicia faba and Commelina communis can be made accessible to a patch-clamp pipet by removing a small portion (1–3 [mu]m in diameter) of the guard cell wall using a microbeam of ultraviolet light generated by a nitrogen laser. Using this laser microsurgical technique, we have measured channel activity across plasma membranes of V. faba guard cells in both cell-attached and isolated patch configurations. Measurements made in the inside-out patch configuration revealed two distinct K+-selective channels. Major advantages of the laser microsurgical technique include the avoidance of enzymatic protoplast isolation, the ability to study cell types that have been difficult to isolate as protoplasts or for which enzymatic isolation protocols result in protoplasts not amenable to patch-clamp studies, the maintenance of positional information in single-channel measurements, reduced disruption of cell-wall-mediated signaling pathways, and the ability to investigate intercellular signaling through studies of cells remaining situated within tissue. This content is only available as a PDF. Copyright © 1996 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

Zhang, J. Z.; Santes, C. M.; Engel, M. L.; Gasser, C. S.; Harada, J. J.

doi: 10.1104/pp.110.4.1069pmid: 8934622

Abstract We analyzed DNA sequences that regulate the expression of an isocitrate lyase gene from Brassica napus L. during late embryogenesis and during postgerminative growth to determine whether glyoxysomal function is induced by a common mechanism at different developmental stages. [beta]-Glucuronidase constructs were used both in transient expression assays in B. napus and in transgenic Arabidopsis thaliana to identify the segments of the isocitrate lyase 5[prime] flanking region that influence promoter activity. DNA sequences that play the principal role in activating the promoter during post-germinative growth are located more than 1200 bp upstream of the gene. Distinct DNA sequences that were sufficient for high-level expression during late embryogenesis but only low-level expression during postgerminative growth were also identified. Other parts of the 5[prime] flanking region increased promoter activity both in developing seed and in seedlings. We conclude that a combination of elements is involved in regulating the isocitrate lyase gene and that distinct DNA sequences play primary roles in activating the gene in embryos and in seedlings. These findings suggest that different signals contribute to the induction of glyoxysomal function during these two developmental stages. We also showed that some of the constructs were expressed differently in transient expression assays and in transgenic plants. This content is only available as a PDF. Copyright © 1996 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

Adam, E.; Kozma-Bognar, L.; Kolar, C.; Schafer, E.; Nagy, F.

doi: 10.1104/pp.110.4.1081pmid: 12226242

Abstract We have isolated a genomic clone from Nicotiana tabacum, designated Nt-PHYB-1, encoding a type-II, “green tissue” phytochrome apoprotein. Recombinant genes, consisting of the 3319-bp promoter of the Nt-PHYB-1 gene (including the entire 5[prime] untranslated sequence but not the ATG) or its deletion derivatives and the bacterial [beta]-glucuronidase reporter gene, were constructed and transferred into tobacco. The expression patterns and levels of the endogenous Nt-PHYB-1, as well as those of the transgenes, were determined by RNase protection assays and by [beta]-glucuronidase histochemical staining. We show that (a) the PHYB-1 gene has three transcription start sites, (b) the abundance of the three PHYB-1-specific mRNAs is different, and that (c) it is not regulated by light. However, we do demonstrate that transcription of the endogenous PHYB-1 gene and that of the recombinant genes exhibit a well-defined organ and tissue specificity. This tobacco PHYB gene is relatively highly expressed in leaf, stem, and different floral organs but not in root. Deletion analysis of the Nt-PHYB-1 promoter indicates that a 382-bp region, located between -1472 and -1089, is required for high-level expression of this gene. This content is only available as a PDF. Copyright © 1996 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

Marrison, J. L.; Schunmann, PHD.; Ougham, H. J.; Leech, R. M.

doi: 10.1104/pp.110.4.1089pmid: 12226243

Abstract The coordination of the synthesis of chlorophyll (Chl) and light-harvesting Chl proteins was determined by observing the sequence of appearance of the specific mRNAs for the nuclear genes CHLH, Por, and Lhcb1*2 (AB180). CHLH encodes a magnesium protoporphyrin chelatase subunit that is involved in the first committed step in Chl biosynthesis; Por encodes protochlorophyllide oxidoreductase, which catalyzes the penultimate and only light-dependent step in Chl biosynthesis; and Lhcb1*2 encodes light-harvesting Chl a/b binding protein of the type-1 light-harvesting complex of photosystem II. Using digoxigenin-labeled antisense and sense RNA probes and a highly sensitive in situ hybridization technique, we have visualized the first appearance of the specific mRNAs in postmitotic mesophyll cells of developing 7-d-old wheat leaves (Triticum aestivum cv Maris dove). The transcripts for CHLH and POR are detectable in the youngest (18 h postmitotic) leaf tissue containing dividing cells; light-harvesting complex of photosystem II transcripts appear 12 h later. This is consistent with a requirement for accumulation of Chl before synthesis of Chl a/b binding protein can proceed at a high rate. All of the transcripts are most abundant in mesophyll cells. In the first leaf the POR message is initially restricted to the palisade, but 12 h later it is also present in the spongy mesophyll cells. All three transcripts aggregated around the surface of the chloroplasts, suggesting that translation may occur preferentially in the vicinity of the target organelle for the primary translation products. This content is only available as a PDF. Copyright © 1996 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

Zhong, H.; Sun, B.; Warkentin, D.; Zhang, S.; Wu, R.; Wu, T.; Sticklen, M. B.

doi: 10.1104/pp.110.4.1097pmid: 12226244

Abstract We have developed a novel and reproducible system for recovery of fertile transgenic maize (Zea mays L.) plants. The transformation was performed using microprojectile bombardment of cultured shoot apices of maize with a plasmid carrying two linked genes, the Streptomyces hygroscopicus phosphinothricin acetyltransferase gene (bar) and the potato proteinase inhibitor II gene, either alone or in combination with another plasmid containing the 5[prime] region of the rice actin 1 gene fused to the Escherichia coli [beta]-glucuronidase gene (gus). Bombarded shoot apices were subsequently multiplied and selected under 3 to 5 mg/L glufosinate ammonium. Co-transformation frequency was 100% (146/146) for linked genes and 80% (41/51) for unlinked genes. Co-expression frequency of the bar and gus genes was 57% (29/51). The co-integration, co-inheritance, and co-expression of bar, the potato proteinase inhibitor II gene, and gus in transgenic R0, R1, and R2 plants were confirmed. Localized expression of the actin 1-GUS protein in the R0 and R1 plants was extensively analyzed by histochemical and fluorometric assays. This content is only available as a PDF. Copyright © 1996 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

Fisher, R. H.; Barton, M. K.; Cohen, J. D.; Cooke, T. J.

doi: 10.1104/pp.110.4.1109pmid: 12226245

Abstract We have isolated an allele of fass, an Arabidopsis thaliana mutation that separates plant development and organ differentiation from plant elongation, and studied its hormonal regulation. Micro-surgically isolated fass roots elongate 2.5 times as much as the roots on intact mutant plants. Wild-type heart embryos, when cultured with a strong auxin, naphthaleneacetic acid, phenocopy fass embryos. fass seedlings contain variable levels of free auxin, which average 2.5 times higher than wild-type seedling levels, and fass seedlings evolve 3 times as much ethylene as wild-type seedlings on a per-plant basis over a 24-h period. The length-to-width ratios of fass seedlings can be changed by several compounds that affect their endogenous ethylene levels, but fass is epistatic to etr1, an ethylene-insensitive mutant. fass's high levels of free auxin may be inducing its high levels of ethylene, which may, in turn, result in the fass phenotype. We postulate that FASS may be acting as a negative regulator to maintain wild-type auxin levels and that the mutation may be in an auxin-conjugating enzyme. This content is only available as a PDF. Copyright © 1996 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

Graham, T. L.; Graham, M. Y.

doi: 10.1104/pp.110.4.1123pmid: 12226246

Abstract The spatial and temporal deployment of plant defense responses involves a complex interplay of signal events, often resulting in superimposition of signaling processes. We have employed a minimal-wound protocol to clearly separate and characterize the specific contributions of light, wounding, and a wall glucan elicitor preparation (PWG) from Phytophthora sojae (Kauf. and Gerde.) to the regulation of phenylpropanoid defense responses in soybean (Glycine max L. [Merr.]) cotyledon tissues. The assay also allowed us to clearly reconstitute responses to combinations of these primary signals and to examine the effects of other pathogenesis-related molecules on the responses in a defined manner. Light specifically triggers accumulation of malonylglucosyl conjugates of the 5-hydroxy-isoflavone, genistein, which is normally found in epidermal cells. PWG selectively induces accumulation of conjugates of the 5-deoxy-isoflavone daidzein, the first committed precursor of the phytoalexin glyceollin. Wounding initiates phenolic polymer deposition, a process greatly potentiated by PWG and light. Whereas glutathione selectively enhances light induction of genistein conjugates, methyl jasmonate enhances both light and PWG-induced isoflavone conjugate accumulations. Wound exudate fully activates the cell's capacity (competency) for the phenolic polymer and glyceollin responses to PWG, whereas glutathione partially restores competency, favoring coumestrol and phenolic polymer responses to PWG. Abscisic acid inhibits all induced phenylpropanoid responses. This content is only available as a PDF. Copyright © 1996 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

Jiang, L.; Abrams, S. R.; Kermode, A. R.

doi: 10.1104/pp.110.4.1135pmid: 12226247

Abstract In transgenic tobacco (Nicotiana tabacum L.) seed, expression of chimeric [beta]-glucuronidase (GUS) genes containing the vicilin or napin storage-protein gene promoters is responsive to premature drying and declines upon rehydration (L. Jiang, W.L. Downing, C.L. Baszczynski, A.R. Kermode [1995] Plant Physiol 107: 1439–1449). Desiccation may cause changes in the content of or sensitivity to abscisic acid (ABA), partially or wholly removing the effects of this “modulator” of developmental gene expression. We studied the enhancement of GUS reporter enzyme activities in transgenic tobacco by exogenous ABA before and after drying. A racemic mixture of ABA at 10 [mu]M caused a 2- to 3-fold increase in GUS activity in developing transgenic seed expressing chimeric genes containing the vicilin or napin gene promoters. However, when these seeds were prematurely dried prior to their culture on ABA medium, enhancement of GUS activity was virtually abolished. Use of optically pure ABAs revealed that the enhancement in GUS activity in developing fresh seed was due largely to the natural (+) form of ABA. Chimeric constructs containing a viral 35S promoter did not respond to ABA whether or not premature drying was applied. Thus, vicilin and napin chimeric genes, initially sensitive to ABA, become relatively insensitive to the hormone following drying. A decline in ABA sensitivity may be an important factor in the cessation of storage-protein gene expression. This content is only available as a PDF. Copyright © 1996 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)