Novel molecular markers for late phases of the growth cycle of Arabidopsis thaliana cell-suspension cultures are expressed during organ senescence

被引:104
作者
Callard, D
Axelos, M
Mazzolini, L
机构
[1] LAB BIOL MOL RELAT PLANTES MICROORGANISMES,CNRS,UNITE MIXTE RECH 215,F-31326 CASTANET TOLOSAN,FRANCE
[2] INRA,F-31326 CASTANET TOLOSAN,FRANCE
关键词
D O I
10.1104/pp.112.2.705
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
In an Arabidopsis thaliana T87-C3 cell-suspension culture, entry into the growth-arrest phase is rapidly followed by a loss of cell viability. Three cDNA clones, SRG1, SRG2, and SRG3, corresponding to genes with transcripts that accumulate during these late phases, were isolated by the mRNA differential display method. Amino acid sequence analysis shows that the putative SRC1 protein is a new member of the Fe(II)/ascorbate oxidase superfamily, and that SRG2 codes for a protein with significant homology to beta-glucosidases. Significantly, all three SRC genes are expressed in senescing organs of Arabidopsis plants. Two previously characterized genes, SAG2 and SAG4, induced during natural senescence in Arabidopsis, were also found to be expressed in cell-suspension cultures and have expression kinetics similar to those observed for the SRG1 gene. Taken together these findings suggest that certain molecular events are common to both plant senescence and growth arrest in Arabidopsis cell suspensions. Both internucleosomal cleavage of nDNA and an apparent compaction of chromatin, two characteristic features of programmed cell death in animal cells, have been observed in Arabidopsis cell cultures at a stage corresponding to loss of cell viability.
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收藏
页码:705 / 715
页数:11
相关论文
共 49 条
[31]   RIPENING-RELATED GENE FROM AVOCADO FRUIT - ETHYLENE-INDUCIBLE EXPRESSION OF THE MESSENGER-RNA AND POLYPEPTIDE [J].
MCGARVEY, DJ ;
SIREVAG, R ;
CHRISTOFFERSEN, RE .
PLANT PHYSIOLOGY, 1992, 98 (02) :554-559
[32]   Sacrifice in the face of foes: Pathogen-induced programmed cell death in plants [J].
Mittler, R ;
Lam, E .
TRENDS IN MICROBIOLOGY, 1996, 4 (01) :10-15
[33]   IN-SITU DETECTION OF NDNA FRAGMENTATION DURING THE DIFFERENTIATION OF TRACHEARY ELEMENTS IN HIGHER-PLANTS [J].
MITTLER, R ;
LAM, E .
PLANT PHYSIOLOGY, 1995, 108 (02) :489-493
[34]   CYANOGENESIS IN PLANTS [J].
POULTON, JE .
PLANT PHYSIOLOGY, 1990, 94 (02) :401-405
[35]   SOCIAL CONTROLS ON CELL-SURVIVAL AND CELL-DEATH [J].
RAFF, MC .
NATURE, 1992, 356 (6368) :397-400
[36]   CDNA CLONING AND EXPRESSION OF AN ARABIDOPSIS GTP-BINDING PROTEIN OF THE ARF FAMILY [J].
REGAD, F ;
BARDET, C ;
TREMOUSAYGUE, D ;
MOISAN, A ;
LESCURE, B ;
AXELOS, M .
FEBS LETTERS, 1993, 316 (02) :133-136
[37]   INDUCTION OF APOPLASTIC INVERTASE OF CHENOPODIUM-RUBRUM BY D-GLUCOSE AND A GLUCOSE ANALOG AND TISSUE-SPECIFIC EXPRESSION SUGGEST A ROLE IN SINK-SOURCE REGULATION [J].
ROITSCH, T ;
BITTNER, M ;
GODT, DE .
PLANT PHYSIOLOGY, 1995, 108 (01) :285-294
[38]  
Sambrook J., 2002, MOL CLONING LAB MANU
[39]   DNA SEQUENCING WITH CHAIN-TERMINATING INHIBITORS [J].
SANGER, F ;
NICKLEN, S ;
COULSON, AR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (12) :5463-5467
[40]   CONTROL OF TRANSCRIPTION AND MESSENGER-RNA TURNOVER AS MECHANISMS OF METABOLIC REPRESSION OF ALPHA-AMYLASE GENE-EXPRESSION [J].
SHEU, JJ ;
JAN, SP ;
LEE, HT ;
YU, SM .
PLANT JOURNAL, 1994, 5 (05) :655-664