Online citations, reference lists, and bibliographies.

Expression Of Catalase And Retinoblastoma-related Protein Genes Associates With Cell Death Processes In Scots Pine Zygotic Embryogenesis

J. Vuosku, S. Sutela, Johanna Kestilä, A. Jokela, T. Sarjala, H. Häggman
Published 2015 · Medicine, Biology

Cite This
Download PDF
Analyze on Scholarcy
Share
BackgroundThe cell cycle and cellular oxidative stress responses are tightly controlled for proper growth and development of Scots pine (Pinus sylvestris L.) seed. Programmed cell death (PCD) is an integral part of the embryogenesis during which megagametophyte cells in the embryo surrounding region (ESR) and cells in the nucellar layers face death. In the present study, we show both the tissue and developmental stage specific expression of the genes encoding the autophagy related ATG5, catalase (CAT), and retinoblastoma related protein (RBR) as well as the connection between the gene expressions and cell death programs.ResultsWe found strong CAT expression in the cells of the developing embryo throughout the embryogenesis as well as in the cells of the megagametophyte and the nucellar layers at the early embryogeny. The CAT expression was found to overlap with both the ATG5 expression and hydrogen peroxide localization. At the late embryogeny, CAT expression diminished in the dying cells of the nucellar layers as well as in megagametophyte cells, showing the first signs of incipient cell death. Accumulation of starch and minor RBR expression were characteristic of megagametophyte cells in the ESR, whereas strong RBR expression was found in the cells of the nucellar layers at the late embryogeny.ConclusionsOur results suggest that ATG5, CAT, and RBR are involved in the Scots pine embryogenesis and cell death processes. CAT seems to protect cells against hydrogen peroxide accumulation and oxidative stress related cell death especially during active metabolism. The opposite expression of RBR in the ESR and nucellar layers alongside morphological characteristics emphasizes the different type of the cell death processes in these tissues. Furthermore, the changes in ATG5 and RBR expressions specifically in the megagametophyte cells dying by necrotic cell death suggest the genetic regulation of developmental necrosis in Scots pine embryogenesis.
This paper references
10.1073/pnas.93.22.12094
Programmed cell death: a way of life for plants.
J. Greenberg (1996)
10.1007/BF02418201
The morphological background to imbibition in seeds ofPinus sylvestris L. of different provenances
E. Tillman-Sutela (2006)
10.1038/sj.cdd.4401068
Programmed cell death eliminates all but one embryo in a polyembryonic plant seed
L. Filonova (2002)
10.1146/ANNUREV.GENET.40.110405.090431
Cell cycle regulation in plant development.
D. Inzé (2006)
10.1006/anbo.1993.1097
Flow Cytometric Determination of Nuclear Replication Stage in Seed Tissues
R. Bino (1993)
Orthodox and Recalcitrant Seeds
10.1093/PCP/PCM009
Glycosyl hydrolases of cell wall are induced by sugar starvation in Arabidopsis.
E. Lee (2007)
10.1007/s102650200019
Programmed cell death of Pinus nucellus in response to pollen tube penetration
R. Hiratsuka (2002)
10.18637/JSS.V014.I09
GETTING STARTED WITH THE R COMMANDER: A BASIC-STATISTICS GRAPHICAL USER INTERFACE TO R
J. Fox (2004)
10.1104/pp.106.083030
Consistency of Polyamine Profiles and Expression of Arginine Decarboxylase in Mitosis during Zygotic Embryogenesis of Scots Pine1
J. Vuosku (2006)
10.1101/GAD.1376506
Necrotic death as a cell fate.
Wei-Xing Zong (2006)
10.1002/j.1537-2197.1993.tb15360.x
Genome size and environmental factors in the genus Pinus
Izumi Wakamiya (1993)
Tropical tree seed manual.
J. A. Vozzo (2002)
10.1074/jbc.270.26.15789
Biochemical and Molecular Characterization of a Barley Seed β-Glucosidase (*)
R. Leah (1995)
10.1111/j.1744-7909.2010.00961.x
Starch synthesis and programmed cell death during endosperm development in triticale (x Triticosecale Wittmack).
C. Li (2010)
ß - Glucosidases
Cairns JRK
10.1093/aobpla/pls014
Hydrogen peroxide—a central hub for information flow in plant cells
V. Petrov (2012)
10.1023/A:1026588408152
Programmed cell death during endosperm development
T. E. Young (2004)
10.1038/sj.cdd.4401724
Classification of cell death: recommendations of the Nomenclature Committee on Cell Death
G. Kroemer (2005)
10.1086/333566
Origin of Cleavage Polyembryony in Conifers
J. T. Buchholz
10.1016/J.PLANTSCI.2009.09.012
Regulation and function of retinoblastoma-related plant genes
P. Sabelli (2009)
Emerging roles of RETINOBLASTOMARELATED proteins in evolution and plant development
R Gutzat (2012)
10.1104/pp.103.2.477
Purification and Characterization of Catalase from Loblolly Pine (Pinus taeda L.) Megagametophytes
R. T. Mullen (1993)
10.1007/s001220050488
Flow cytometric evidence for multiple ploidy levels in the endosperm of some gymnosperm species
C. Pichot (1997)
10.1083/jcb.201307082
Autophagy and metacaspase determine the mode of cell death in plants
E. Minina (2013)
10.1023/A:1006134027834
Analysis of programmed cell death in wheat endosperm reveals differences in endosperm development between cereals
T. E. Young (2004)
10.1093/aob/mct184
Ricinosomes provide an early indicator of suspensor and endosperm cells destined to die during late seed development in quinoa (Chenopodium quinoa).
M. López-Fernández (2013)
Metacaspases. Cell Death Differ
L Tsiatsiani (2011)
10.1023/A:1025008117046
Proteases associated with programmed cell death of megagametophyte cells after germination of white spruce (Picea glauca) seeds
X. He (2004)
10.1111/j.1365-3040.2011.02387.x
Redox regulation in plant programmed cell death.
M. D. de Pinto (2012)
Orthodox and recalcitrant seeds. In Vozzo JA, editor. Tropical tree seed manual. Washington DC, USA: USDA Forest Service; 2003:137–47
P Berjak (2003)
10.1104/pp.106.078295
Reactive Oxygen Species in Plant Cell Death1
F. Van Breusegem (2006)
BMC Plant Biology
Nicolas Ranc (2003)
10.1073/PNAS.95.10.5818
Defense activation and enhanced pathogen tolerance induced by H2O2 in transgenic tobacco.
S. Chamnongpol (1998)
10.1016/J.TIBS.2006.11.001
Cell death by necrosis: towards a molecular definition.
P. Golstein (2007)
10.1007/s10725-004-2601-8
Biochemical changes during seed development in Pinus taeda L.
V. Silveira (2004)
10.1093/JXB/ERR196
Classes of programmed cell death in plants, compared to those in animals
W. Doorn (2011)
10.4161/psb.4.10.9535
Pine embryogenesis
J. Vuosku (2009)
Investigations on the flowering and seed crop of Pinus silvestris.
R. Sarvas (1962)
10.1080/07352680802467744
Programmed Cell Death in Plants: Orchestrating an Intrinsic Suicide Program Within Walls
E. Lam (2008)
10.1016/J.PLANTSCI.2006.12.014
Conserved functions of retinoblastoma proteins: From purple retina to green plant cells
P. Miskolczi (2007)
Reactive oxygen species in plant cell death
F VanBreusegem (2006)
10.1023/A:1005742916292
cDNA cloning and differential gene expression of three catalases in pumpkin
M. Esaka (1997)
10.1093/pcp/pcq130
Programmed cell death of the megagametophyte during post-germinative growth of white spruce (Picea glauca) seeds is regulated by reactive oxygen species and the ubiquitin-mediated proteolytic system.
X. He (2010)
10.1101/gad.1829209
Endoreplication: polyploidy with purpose.
H. Lee (2009)
10.1023/A:1026584207243
Programmed cell death in cereal aleurone
A. Fath (2004)
Transcription of cRNA for in situ hybridization from polymerase chain reaction-amplified DNA.
I. D. Young (1991)
10.1104/pp.112.1.327
Catalase Is Encoded by a Multigene Family in Arabidopsis thaliana (L.) Heynh
J. Frugoli (1996)
10.1093/JXB/ERH050
Catalase activity and expression in developing sunflower seeds as related to drying.
C. Bailly (2004)
10.1093/JXB/ERG021
Redox regulation and storage processes during maturation in kernels of Triticum durum.
L. De Gara (2003)
10.1093/JXB/50.337.1359
Water content, lipid deposition, and (+)-abscisic acid content in developing white spruce seeds
D. J. Carrier (1999)
10.1093/jxb/erp020
One tissue, two fates: different roles of megagametophyte cells during Scots pine embryogenesis
J. Vuosku (2009)
10.1016/j.crvi.2008.07.022
From intracellular signaling networks to cell death: the dual role of reactive oxygen species in seed physiology.
C. Bailly (2008)
10.1007/BF00202017
The significance of structure for imbibition in seeds of the Norway spruce, Picea abies (L.) Karst.
E. Tillman-Sutela (1995)
10.1093/treephys/tps088
Polyamine metabolism during exponential growth transition in Scots pine embryogenic cell culture.
J. Vuosku (2012)
10.1007/BF00306214
Protein staining of ribboned epon sections for light microscopy
D. Fisher (2004)
10.1046/J.1365-313X.2003.01655.X
Changes in hydrogen peroxide homeostasis trigger an active cell death process in tobacco.
J. Dat (2003)
10.1038/cdd.2011.36
Morphological classification of plant cell deaths
W. V. Doorn (2011)
10.1073/pnas.2136610100
A comprehensive analysis of hydrogen peroxide-induced gene expression in tobacco
Steven Vandenabeele (2003)
10.1016/S0168-9452(99)00194-6
DIFFERENTIAL DIURNAL EXPRESSION OF RICE CATALASE GENE : THE 5'-FLANKING REGION OF CatA IS NOT SUFFICIENT FOR CIRCADIAN CONTROL
M. Iwamoto (2000)
10.1016/j.cub.2004.04.019
Metacaspase-dependent programmed cell death is essential for plant embryogenesis
M. F. Suárez (2004)
10.1007/BF02352287
Molecular evolution of maize catalases and their relationship to other eukaryotic and prokaryotic catalases
L. Guan (2006)
10.1073/pnas.1304903110
Control of cell proliferation, endoreduplication, cell size, and cell death by the retinoblastoma-related pathway in maize endosperm
P. Sabelli (2013)
Botanical histochemistry
WA Jensen (1962)
Programmed cell death eliminates all but one embryo in a polyembryonic plant
LH Filonova (2002)
10.1038/sj.cdd.4401330
VEIDase is a principal caspase-like activity involved in plant programmed cell death and essential for embryonic pattern formation
P. Bozhkov (2004)
10.1186/1746-4811-6-7
Dealing with the problem of non-specific in situ mRNA hybridization signals associated with plant tissues undergoing programmed cell death
J. Vuosku (2009)
10.1080/10618600.1996.10474713
Gentleman R: R: A language for data analysis and graphics
Ross Ihaka (1996)
10.1093/aob/mcr098
Distribution of gluten proteins in bread wheat (Triticum aestivum) grain.
P. Tosi (2011)
10.1146/ANNUREV.ARPLANT.58.032806.103946
Oxidative modifications to cellular components in plants.
I. M. Møller (2007)
10.1105/tpc.9.7.1157
Programmed Cell Death in Plants.
R. Pennell (1997)
10.1093/jxb/err196
Classes of programmed cell death in plants, compared to those in animals.
W. G. van Doorn (2011)
10.1007/BF02277422
Catalases in plants
H. Willekens (1995)
10.1104/PP.125.1.94
Programmed cell death in development and defense.
A. Jones (2001)
10.1016/J.TPLANTS.2004.08.007
More than a yolk: the short life and complex times of the plant endosperm.
Liliana M. Costa (2004)
10.1016/j.tplants.2011.12.001
Emerging roles of RETINOBLASTOMA-RELATED proteins in evolution and plant development.
Ruben Gutzat (2012)
10.1038/323643a0
A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma
S. Friend (1986)
10.1038/nrm3737
Regulated necrosis: the expanding network of non-apoptotic cell death pathways
T. V. Berghe (2014)
10.1093/jxb/erq282
Catalase function in plants: a focus on Arabidopsis mutants as stress-mimic models.
Amna Mhamdi (2010)
10.1105/tpc.113.117192
Catalase and NO CATALASE ACTIVITY1 Promote Autophagy-Dependent Cell Death in Arabidopsis[C][W][OPEN]
Thomas Hackenberg (2013)
10.4161/cc.5.4.2428
Grasses Like Mammals? Redundancy and Compensatory Regulation within the Retinoblastoma Protein Family
P. Sabelli (2006)
10.1046/J.1365-313X.1999.00413.X
Specific checkpoints regulate plant cell cycle progression in response to oxidative stress
Jean-Philippe Reichheld (1999)
10.1007/s00425-005-1562-0
Evaluation of control transcripts in real-time RT-PCR expression analysis during maritime pine embryogenesis
S. Gonçalves (2005)
10.1006/ANBO.1998.0655
Hydrogen Peroxide Production is a General Property of the Lignifying Xylem from Vascular Plants
A. Barceló (1998)
10.1016/S0168-9452(97)00178-7
Changes in carbohydrate composition and α-amylase expression during germination and seedling growth of starch-deficient endosperm mutants of maize
T. E. Young (1997)
10.1111/pce.12053
Down-regulation of catalase activity allows transient accumulation of a hydrogen peroxide signal in Chlamydomonas reinhardtii.
Laure Michelet (2013)
10.1021/pr900954p
Integrated proteomic and cytological study of rice endosperms at the storage phase.
Sheng bao Xu (2010)
10.1038/cdd.2011.37
Programmed cell death in the plant immune system
N. Coll (2011)
Embryology of gymnosperms
Hardev Singh (1978)
10.1104/pp.105.065896
Genome-Wide Analysis of Hydrogen Peroxide-Regulated Gene Expression in Arabidopsis Reveals a High Light-Induced Transcriptional Cluster Involved in Anthocyanin Biosynthesis1[w]
Sandy Vanderauwera (2005)
10.1146/ANNUREV.ARPLANT.55.031903.141701
Reactive oxygen species: metabolism, oxidative stress, and signal transduction.
K. Apel (2004)
10.1038/cdd.2008.150
Classification of cell death: recommendations of the Nomenclature Committee on Cell Death 2009
G. Kroemer (2009)
10.1093/treephys/15.7-8.485
Abscisic acid and zygotic embryogenesis in Pinus taeda.
R. H. Kapik (1995)
10.1016/S0065-230X(01)82001-7
Retinoblastoma protein partners.
E. Morris (2001)
10.1016/j.abb.2012.04.015
Plant catalases: peroxisomal redox guardians.
Amna Mhamdi (2012)
Orthodox and recalcitrant seeds Tropical tree seed manual
P Berjak (2003)
Cell Mol Life Sci
Jrk Cairns (2010)
10.1111/j.1399-3054.2009.01327.x
Senescence-induced loss in photosynthesis enhances cell wall beta-glucosidase activity.
Pranab Kishor Mohapatra (2010)
10.1046/J.1365-313X.2002.01427.X
Double antisense plants lacking ascorbate peroxidase and catalase are less sensitive to oxidative stress than single antisense plants lacking ascorbate peroxidase or catalase.
L. Rizhsky (2002)
10.1038/nature02637
Plant retinoblastoma homologues control nuclear proliferation in the female gametophyte
C. Ebel (2004)



This paper is referenced by
Semantic Scholar Logo Some data provided by SemanticScholar