Transcriptional regulation of proline biosynthesis in Medicago truncatula reveals developmental and environmental specific features

被引:215
作者
Armengaud, P
Thiery, L
Buhot, N
Grenier-de March, G
Savouré, A
机构
[1] Univ Paris 06, CNRS, UMR 7632, Lab Physiol Cellulaire & Mol Plantes, F-75252 Paris 05, France
[2] Univ Picardie, Ctr Ressources Reg Biol Mol, F-80039 Amiens, France
[3] Inst Super Agr Beauvais, Lab Biotechnol Vegetales, F-60026 Beauvais, France
关键词
D O I
10.1111/j.0031-9317.2004.00251.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The model legume plant Medicago truncatula accumulates free proline in response to hyperosmotic stress as do many other organisms. In order to analyse the transcriptional regulation of proline biosynthesis in M. truncatula, three cDNAs encoding Delta(1)-pyrroline-5-carboxylate synthetase (P5CS1, P5CS2; EC not assigned) and ornithine delta-aminotransferase (OAT; EC 2.6.1.13) were isolated. The cDNAs shared high homologies with the other plant sequences and genomic organization analysis indicated the presence of two P5CS and two putative OAT genes. The two P5CS genes showed differing transcript level regulation according to organs and in response to osmotic stress. MtP5CS1 steady-state transcript levels in the different plant organs were correlated with proline levels but transcript abundance was unaffected by osmotic stresses. MtP5CS2 transcripts were poorly detected in all organs but were strongly accumulated in shoots of salt-stressed plants. We suggest a specific of MtP5CS1 and MtP5CS2 as a housekeeping product and as a stress specific isoform, respectively. MtOAT transcripts were predominantly detected in roots and shoots of unstressed plants. Salt-stress treatment induced the accumulation of MtOAT transcripts in the whole plant whatever the developmental stage. In salt-stressed roots, a positive correlation was found between proline and MtOAT transcript accumulation. These results suggest that both ornithine and glutamate biosynthesis pathways contribute to the osmotic stress-induced proline accumulation in M. truncatula.
引用
收藏
页码:442 / 450
页数:9
相关论文
共 40 条
[1]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[2]   Subcellular compartmentation of proline in the leaves of the subantarctic Kerguelen cabbage Pringlea antiscorbutica R-Br. in vivo 13C-NMR study [J].
Aubert, S ;
Hennion, F ;
Bouchereau, A ;
Gout, E ;
Bligny, R ;
Dorne, AJ .
PLANT CELL AND ENVIRONMENT, 1999, 22 (03) :255-259
[3]   RAPID DETERMINATION OF FREE PROLINE FOR WATER-STRESS STUDIES [J].
BATES, LS ;
WALDREN, RP ;
TEARE, ID .
PLANT AND SOIL, 1973, 39 (01) :205-207
[4]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[5]  
DELAUNEY AJ, 1993, J BIOL CHEM, V268, P18673
[6]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[7]  
Doyle JJ., 1987, FOCUS, V19, P11, DOI DOI 10.2307/2419362
[8]   Comparative analysis of the regulation of expression and structures of two evolutionarily divergent genes for Δ1-pyrroline-5-carboxylate synthetase from tomato [J].
Fujita, T ;
Maggio, A ;
Garcia-Rios, M ;
Bressan, RA ;
Csonka, LN .
PLANT PHYSIOLOGY, 1998, 118 (02) :661-674
[9]   Cloning of a polycistronic cDNA from tomato encoding gamma-glutamyl kinase and gamma-glutamyl phosphate reductase [J].
GarciaRios, M ;
Fujita, T ;
LaRosa, PC ;
Locy, RD ;
Clithero, JM ;
Bressan, RA ;
Csonka, LN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (15) :8249-8254
[10]   Isolation and characterization of two different cDNAs of Δ1-pyrroline-5-carboxylate synthase in alfalfa, transcriptionally induced upon salt stress [J].
Ginzberg, I ;
Stein, H ;
Kapulnik, Y ;
Szabados, L ;
Strizhov, N ;
Schell, J ;
Koncz, C ;
Zilberstein, A .
PLANT MOLECULAR BIOLOGY, 1998, 38 (05) :755-764