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Markers For Hypersensitive Response And Senescence Show Distinct Patterns Of Expression

D. Pontier, S. Gan, R. Amasino, D. Roby, Eric Lam
Published 2004 · Biology, Medicine

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Controlled cellular suicide is an important process that can be observed in various organs during plant development. From the generation of proper sexual organs in monoecious plants to the hypersensitive response (HR) that occurs during incompatible pathogen interactions, programmed cell death (PCD) can be readily observed. Although several biochemical and morphological parameters have been described for various types of cell death in plants, the relationships existing between those different types of PCD events remain unclear. In this work, we set out to examine if two early molecular markers of HR cell death (HIN1 and HSR203J) as well as a senescence marker (SAG12) are coordinately induced during these processes. Our result indicates that although there is evidence of some cross-talk between both cell death pathways, spatial and temporal characteristics of activation for these markers during hypersensitive response and senescence are distinct. These observations indicate that these markers are relatively specific for different cell death programs. Interestingly, they also revealed that a senescence-like process seems to be triggered at the periphery of the HR necrotic lesion. This suggests that cells committed to die during the HR might release a signal able to induce senescence in the neighboring cells. This phenomenon could correspond to the establishment of a second barrier against pathogens. Lastly, we used those cell death markers to better characterize cell death induced by copper and we showed that this abiotic induced cell death presents similarities with HR cell death.
This paper references
10.1094/MPMI-3-417
Characterization of the masked strain of tobacco mosaic virus: identification of the region responsible for symptom attenuation by analysis of an infectious cDNA clone.
C. Holt (1990)
10.1139/b88-087
A comparison of the death induced by fungal invasion or toxic chemicals in cowpea epidermal cells. I: Cell death induced by heavy metal salts
S. L. Meyer (1988)
10.1101/GAD.12.9.1304
Defects in regulation of apoptosis in caspase-2-deficient mice.
L. Bergeron (1998)
Fruit-specific expression of theA
B Martineau (1994)
10.1016/0042-6822(64)90298-3
THE INFLUENCE OF KINETIN ON TOBACCO MOSAIC VIRUS PRODUCTION IN NICOTIANA GLUTINOSA LEAF DISKS.
Z. Király (1964)
10.1016/S0168-9525(97)01126-8
Facing death in the fly: genetic analysis of apoptosis in Drosophila.
K. McCall (1997)
10.1105/tpc.8.3.393
Cleavage of Nuclear DNA into Oligonucleosomal Fragments during Cell Death Induced by Fungal Infection or by Abiotic Treatments.
D. Ryerson (1996)
10.1007/s004380050563
Differential activation of two ACC oxidase gene promoters from melon during plant development and in response to pathogen attack
É. Lasserre (1997)
10.1016/S0048-4059(72)80004-3
Suppression of the bacterially induced hypersensitive reaction by cytokinins
A. Novacký (1972)
Absorption of light by chlorophyll solutions
G. Mackinney (1941)
10.1128/jb.168.2.512-522.1986
Gene cluster of Pseudomonas syringae pv. "phaseolicola" controls pathogenicity of bean plants and hypersensitivity of nonhost plants.
P. B. Lindgren (1986)
10.1073/pnas.93.22.12094
Programmed cell death: a way of life for plants.
J. Greenberg (1996)
10.1046/j.1365-313X.1994.05040507.x
hsr203J, a tobacco gene whose activation is rapid, highly localized and specific for incompatible plant/pathogen interactions.
D. Pontier (1994)
A comparison of the cell death induced by fungal invasion or toxic chemicals in cowpea epidermal cells
SLF Meyer (1988)
10.1105/tpc.9.7.1157
Programmed Cell Death in Plants.
R. Pennell (1997)
10.1038/sj.cdd.4400309
The hypersensitive response and the induction of cell death in plants
J. Morel (1997)
10.1016/S0968-0004(97)01107-9
Caspases and caspase inhibitors.
P. Villa (1997)
10.1046/j.1365-313X.1994.5010011.x
Fruit-specific expression of the A. tumefaciens isopentenyl transferase gene in tomato: effects on fruit ripening and defense-related gene expression in leaves
B. Martineau (1994)
10.1105/tpc.7.11.1951
Identification, characterization, and purification of a tobacco endonuclease activity induced upon hypersensitive response cell death.
R. Mittler (1995)
10.1016/S0092-8674(00)80179-8
A Novel Suppressor of Cell Death in Plants Encoded by the Lls1 Gene of Maize
J. Gray (1997)
10.1016/S0959-437X(96)90007-6
Programmed cell death in invertebrates.
M. Hengartner (1996)
10.1139/b88-088
A comparison of the death induced by fungal invasion or toxic chemicals in cowpea epidermal cells. II. Responses induced by Erysiphe cichoracearum
S. L. Meyer (1988)
10.1093/oxfordjournals.pcp.a078561
Oxidative Damage Caused by an Excess of Copper in Oat Leaves
C. Luna (1994)
10.1002/j.1460-2075.1987.tb02730.x
GUS fusions: beta‐glucuronidase as a sensitive and versatile gene fusion marker in higher plants.
R. Jefferson (1987)
10.1016/S0958-1669(97)80103-6
The molecular genetic analysis of leaf senescence.
Nam (1997)
10.1002/j.1460-2075.1987.tb02541.x
The 5′‐proximal region of the wheat Cab‐1 gene contains a 268‐bp enhancer‐like sequence for phytochrome response.
F. Nagy (1987)
10.1046/j.1365-313X.1994.6060879.x
Promoter tagging with a promoterless ipt gene leads to cytokinin-induced phenotypic variability in transgenic tobacco plants:implications of gene dosage effects.
A. Hewelt (1994)
10.1111/J.1432-1033.1997.T01-1-00700.X
Functional expression of a tobacco gene related to the serine hydrolase family -- esterase activity towards short-chain dinitrophenyl acylesters.
E. Baudouin (1997)
10.1126/science.270.5244.1986
Inhibition of Leaf Senescence by Autoregulated Production of Cytokinin
S. Gan (1995)
10.1111/j.1469-8137.1994.tb04243.x
Gene expression during leaf senescence
Catherine H M Smart (1994)
10.1093/jxb/48.2.181
The molecular biology of leaf senescence
V. Buchanan-Wollaston (1997)
10.1016/0012-1606(92)90123-X
Altered morphology in transgenic tobacco plants that overproduce cytokinins in specific tissues and organs.
Y. Li (1992)
10.1023/A:1005727132202
The promoter of the tobacco Tnt1 retrotransposon is induced by wounding and by abiotic stress
C. Mhiri (1997)
10.1111/j.1399-3054.1994.tb05343.x
Molecular analysis of natural leaf senescence in Arabidopsis thaliana
Karin N. Lohman (1994)
10.1016/S0048-4059(83)81014-5
The relationship between stimulated ethylene production and symptom expression in virus-infected tobacco leaves*
A. D. Laat (1983)
10.1016/S0092-8674(00)80934-4
Death-Defying Yeast Identify Novel Apoptosis Genes
S. Shaham (1998)
10.1016/S0960-9822(98)70469-5
Caspases and programmed cell death in the hypersensitive response of plants to pathogens
Olga María del Pozo (1998)
10.1104/pp.113.2.313
Making Sense of Senescence (Molecular Genetic Regulation and Manipulation of Leaf Senescence)
S. Gan (1997)
10.1104/pp.62.4.522
Modification of disease resistance of tobacco callus tissues by cytokinins.
G. Haberlach (1978)
10.1046/j.1365-313X.1996.10040591.x
hrp gene-dependent induction of hin1: a plant gene activated rapidly by both harpins and the avrPto gene-mediated signal.
S. Gopalan (1996)
10.1016/S1360-1385(98)01243-6
Disease resistance: beyond the resistance genes
S. Gopalan (1998)
10.1105/tpc.2.10.999
Activation of a Bean Chitinase Promoter in Transgenic Tobacco Plants by Phytopathogenic Fungi.
D. Roby (1990)
10.1073/pnas.92.14.6597
NDR1, a locus of Arabidopsis thaliana that is required for disease resistance to both a bacterial and a fungal pathogen.
K. C. Century (1995)
10.1094/MPMI.1998.11.6.544
Activation of hsr203, a plant gene expressed during incompatible plant-pathogen interactions, is correlated with programmed cell death.
D. Pontier (1998)
10.1105/tpc.7.1.29
Coordinated Activation of Programmed Cell Death and Defense Mechanisms in Transgenic Tobacco Plants Expressing a Bacterial Proton Pump.
R. Mittler (1995)
10.1016/S0885-5765(05)80080-3
The inhibition of the hypersensitive response of potato tuber tissues by cytokinins, similarities between senescence and plant defence responses*
K. B. Beckman (1994)
10.1126/SCIENCE.278.5345.1963
NDR1, a pathogen-induced component required for Arabidopsis disease resistance.
K. C. Century (1997)



This paper is referenced by
10.1016/J.JPLPH.2005.01.013
The level of jasmonic acid in Arabidopsis thaliana and Phaseolus coccineus plants under heavy metal stress.
W. Maksymiec (2005)
Genome, transcriptome, and methylome in the conifer pathogen Heterobasidion parviporum
Zhen Zeng (2019)
10.1007/S11434-006-1085-5
Identification of genes associated with cotyledon senescence in upland cotton
Shen Fa-fu (2006)
10.1007/s00122-013-2081-1
Identification of genetic markers linked to anthracnose resistance in sorghum using association analysis
H. Upadhyaya (2013)
10.1111/pbi.12237
Pathogen-induced SGT1 of Arachis diogoi induces cell death and enhanced disease resistance in tobacco and peanut.
Dilip Tak Kumar (2015)
10.11606/T.11.2014.tde-11112014-165547
Tnt1 retrotransposon expression and ethylene phytohormone interplay mediates tobacco (Nicotiana tabacum) defense responses
D. Quintanilha (2014)
10.5010/JPB.2009.36.1.045
Identification and characterization of a rice blast fungal elicitor-inducible Oshin1 gene
C. Kim (2009)
AtCOX 17 , an Arabidopsis Homolog of the Yeast Copper Chaperone COX 171
T. Balandin (2002)
10.1007/s10327-004-0164-1
Timing and extent of hypersensitive response are critical to restrict local and systemic spread of Pepper mild mottle virus in pepper containing the L3 gene
H. Hamada (2004)
10.1093/dnares/dsv040
Identification, cloning and characterization of R2R3-MYB gene family in canola (Brassica napus L.) identify a novel member modulating ROS accumulation and hypersensitive-like cell death
Bisi Chen (2016)
10.1094/PHYTO-96-1052
The Internal Glycine-Rich Motif and Cysteine Suppress Several Effects of the HpaG(Xooc) Protein in Plants.
Fengquan Liu (2006)
10.1111/J.1365-313X.2004.02234.X
A subset of hypersensitive response marker genes, including HSR203J, is the downstream target of a spermine signal transduction pathway in tobacco.
Yoshihiro Takahashi (2004)
10.1023/A:1026592509060
Hypersensitive response-related death
M. Heath (2004)
10.1016/J.PLAPHY.2007.09.010
Identification, expression analysis and characterization of defense and signaling genes in Vitis vinifera.
J. Chong (2008)
10.1094/MPMI-12-12-0287-R
Stabilization of cytokinin levels enhances Arabidopsis resistance against Verticillium longisporum.
Michael Reusche (2013)
Understanding the role of L-type lectin receptor kinases in Phytophthora resistance
Y. Wang (2014)
10.1111/mpp.12257
Activation of senescence-associated Dark-inducible (DIN) genes during infection contributes to enhanced susceptibility to plant viruses.
L. Fernández-Calvino (2016)
10.1111/AAB.12311
Seed treatment with salicylic acid invokes defence mechanism of Helianthus annuus against Orobanche cumana
Chong Yang (2016)
10.1023/A:1026552827716
Regulators of cell death in disease resistance
K. Shirasu (2004)
10.1002/ETC.5620200626
Synergistic effects of a photooxidized polycyclic aromatic hydrocarbon and copper on photosynthesis and plant growth: evidence that in vivo formation of reactive oxygen species is a mechanism of copper toxicity.
T. S. Babu (2001)
10.1046/J.0960-7412.2001.01228.X
Identification of a novel gene HYS1/CPR5 that has a repressive role in the induction of leaf senescence and pathogen-defence responses in Arabidopsis thaliana.
Satoko Yoshida (2002)
10.1007/978-94-017-3522-3_3
Cells: Functional Units of TCLs
J. Silva (2003)
10.1094/PHYTO-98-5-0519
Genetic resistance to Peronospora tabacina in Nicotiana langsdorffii, a South American wild tobacco.
Shujian Zhang (2008)
10.1897/05-073R.1
Biochemical responses of the aquatic higher plant Lemna gibba to a mixture of copper and 1,2-dihydroxyanthraquinone: synergistic toxicity via reactive oxygen species.
T. S. Babu (2005)
Transcriptional regulatory codes underlying Arabidopsis stress responses
Richard Hickman (2012)
10.1093/PCP/PCE021
Isolation and RNA gel blot analysis of genes that could serve as potential molecular markers for leaf senescence in Arabidopsis thaliana.
S. Yoshida (2001)
10.1034/J.1399-3054.2001.1130101.X
Current molecular understanding of the genetically programmed process of leaf senescence
J. M. Chandlee (2001)
10.1046/J.1432-1033.2003.03630.X
AtCYS1, a cystatin from Arabidopsis thaliana, suppresses hypersensitive cell death.
B. Belenghi (2003)
Biomarcadores de contaminación por cadmio en las plantas
Beatriz Pernía (2008)
Identification of Arabidopsis stay-green mutants with a functional ethylene-response pathway.
Reza Shirzadian-Khorramabad (2010)
10.1093/pcp/pcx184
A Novel NAC-Type Transcription Factor, NAC87, from Oilseed Rape Modulates Reactive Oxygen Species Accumulation and Cell Death
Jingli Yan (2018)
10.1111/j.1365-3040.2011.02442.x
Convergence and divergence in gene expression profiles induced by leaf senescence and 27 senescence-promoting hormonal, pathological and environmental stress treatments.
Yongfeng Guo (2012)
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