A new member of the LIR gene family from perennial ryegrass is cold-responsive, and promotes vegetative growth in Arabidopsis

Plant Science

Volumn 172, Issue 2, 2007, Pages 221-227

  Ciannamea, Stefano ^c   Jensen, Christian Sig ^a,b   Agerskov, Henrik ^b   Petersen, Klaus ^b   Lenk, Ingo ^a   Didion, Thomas ^b   Immink, Richard G H ^c   Angenent, Gerco C ^c   Nielsen, Klaus K ^a,b  

^a DLF Trifolium AS   (Denmark)

^b TECHNICAL UNIVERSITY OF DENMARK   (Denmark)

^c WAGENINGEN UNIVERSITY   (Netherlands)

Author keywords

Arabidopsis; Cold responses; Lolium; Photoperiod

Indexed keywords

GENES; GROWTH KINETICS; RNA;

ARABIDOPSIS; COLD RESPONSES; LOLIUM; PERENNIAL RYEGRASS; PHOTOPERIOD;

PLANTS (BOTANY);

GENES; GROWTH; NUCLEIC ACIDS; PLANTS; TISSUE;

ARABIDOPSIS; LOLIUM; LOLIUM PERENNE;

EID: 33846039212     PISSN: 01689452     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plantsci.2006.08.011     Document Type: Article

References (31)

1. Jensen C.S., Salchert K., and Nielsen K.K. A TERMINAL FLOWER-Like gene from perennial ryegrass involved in floral transition and axillary meristem identity. Plant Physiol. 125 (2001) 1517-1528
2. Macmillan C.P., Blundell C.A., and King R.W. Flowering of the grass Lolium perenne. Effects of vernalization and long days on gibberellin biosynthesis and signalling. Plant Physiol. 138 (2005) 1794-1806
3. Ausín I., Alonso-Blanco C., and Martinez-Zapater J.M. Environmental regulation of flowering. Int. J. Dev. Biol. 49 (2005) 689-705
4. Jensen L.B., Andersen J.R., Frei U., Xing Y., Taylor C., Holm P.B., and Lubberstedt T. QTL mapping of vernalization response in perennial ryegrass (Lolium perenne L.) reveals co-location with an orthologue of wheat VRN1. Theor. Appl. Genet. 110 (2005) 527-536
5. Petersen K., Didion T., Andersen C.H., and Nielsen K.K. MADS-box genes from perennial ryegrass differentially expressed during transition from vegetative to reproductive growth. J. Plant Physiol. 161 (2004) 439-447
6. Petersen K., Kolmos E., Folling M., Salchert K., Storgaard M., Jensen C.S., Didion T., and Nielsen K.K. Two MADS-box genes from perennial ryegrass are regulated by vernalization and involved in the floral transition. Physiol. Plant 126 (2006) 268-278
7. Wanner L.A., and Juntilla O. Cold-induced freezing tolerance in Arabidopsis. Plant Physiol. 120 (1999) 391-400
8. Fowler S., and Thomashow M.F. Arabidopsis transcriptome profiling indicates that multiple regulatory pathways are activated during cold acclimation in addition to the CBF cold response pathway. Plant Cell 14 (2002) 1675-1690
9. Ciannamea S., Busscher-Lange J., de Folter S., Angenent G.C., and Immink R.G.H. Characterization of the vernalization response in Lolium perenne by a cDNA microarray approach. Plant Cell Physiol. 47 (2006) 481-492
10. Kojima S., Takahashi Y., Kobayashi Y., Monna L., Sasaki T., Araki T., and Yano M. Hd3a, a rice ortholog of the Arabidopsis FT gene, promotes transition to flowering downstream of Hd1 under short-day conditions. Plant Cell Physiol. 43 (2000) 1096-1105
11. Yano M., Katayose Y., Ashikari M., Yamanouchi U., Monna L., Fuse T., Baba T., Yamamoto K., Umehara Y., Nagamura Y., and Sasaki T. Hd1, a major photoperiod sensitivity quantitative trait locus in rice, is closely related to the Arabidopsis flowering time gene CONSTANS. Plant Cell 1212 (2000) 2473-2484
12. Hayama R., Izawa T., and Shimamoto K. Isolation of rice genes possibly involved in the photoperiodic control of flowering by a fluorescent differential display method. Plant Cell Physiol. 43 (2002) 494-504
13. Reimmann C., and Dudler R. Circadian rhythmicity in the expression of a novel light-regulated rice gene. Plant Mol. Biol. 22 (1993) 165-170
14. Teramoto H., Momotani E., Takeba G., and Tsuji H. Isolation of a cDNA clone for a cytokinin-repressed gene in excised cucumber cotyledons. Planta 193 (1994) 573-579
15. Abied M.A., and Holland D. Two newly isolated genes from citrus exhibit a different pattern of diurnal expression and light response. Plant Mol. Biol. 26 (1994) 165-173
16. Cohn N.S., Zhang L., Mitchell J.P., and Vierheller C.H.Z. Gibberellin-stimulated changes in abundance of 2 messenger-rnas in the developing shoot of dwarf peas (Pisum sativum L.). Int. J. Plant Sci. 155 (1994) 498-505
17. Quigley F., Dao P., Cottet A., and Mache R. Sequence analysis of an 81 kb contig from Arabidopsis thaliana chromosome III. Nucleic Acids Res. 24 (1996) 4313-4318
18. Wang Z.L., Li P.H., Fredricksen M., Gong Z.Z., Kim C.S., Zhang C., Bohnert H.J., Zhu J.K., Bressan R.A., Hasegawa P.M., Zhao Y.X., and Zhang H. Expressed sequence tags from Thellungiella halophila, a new model to study plant salt-tolerance. Plant Sci. 166 (2004) 609-616
19. Lavery D.J., Lopez-Molina L., Fleury-Olela F., and Schibler U. Selective amplification via biotin- and restriction-mediated enrichment (SABRE), a novel selective amplification procedure for detection of differentially expressed mRNAs. Proc. Natl. Acad. Sci. U.S.A. 94 (1997) 6831-6836
20. Sambrook J., Fritsch E.F., and Maniatis T. Molecular Cloning: A Laboratory Manual (1989), Cold Spring Harbor Laboratory Press, NY
21. Feinberg A.P., and Vogelstein B. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal. Biochem. 137 (1984) 266-267
22. Angenent G.C., Busscher M., Franken J., Mol J.N., and van Tunen A.J. Differential expression of two MADS box genes in wild-type and mutant petunia flowers. Plant Cell 4 (1992) 983-993
23. Koncz C., and Schell J. The promoter of the TL-DNA gene 5 controls the tissue-specific expression of chimeric genes carried by a novel type of Agrobacterium binary vector. Mol. Gen. Genet. 204 (1986) 383-396
24. Clough S.J., and Bent A.F. Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. Plant J. 16 (1998) 735-743
25. Koornneef M., Alanso-Blanco C., Peeters A.J.M., and Soppe W. Genetic control of flowering time in Arabidopsis. Ann. Rev. Plant Physiol. Plant Mol. Biol. 49 (1998) 345-370
26. Zimmermann P., Hirsch-Hoffmann M., Hennig L., and Gruissem W. GENEVESTIGATOR. Arabidopsis microarray database and analysis toolbox. Plant Physiol. 136 (2004) 2621-2632
27. Bläsing O.E., Gibon Y., Gunther M., Höhne M., Morcuende R., Osuna D., Thimm O., Usadel B., Scheibe W.-R., and Stitt M. Sugars and circadian regulation make major contributions to the global regulation of diurnal gene expression in Arabidopsis. Plant Cell 17 (2005) 3257-3281
28. Sheldon C.C., Burn J.E., Perez P.P., Metzger J., Edwards J.A., Peacock W.J., and Dennis E.S. The FLF MADS box gene: a repressor of flowering in Arabidopsis regulated by vernalization and methylation. Plant Cell 11 (1999) 445-458
29. Rawson H.M., Zajac M., and Penrose L.D.J. Effect of seedling temperature and its duration on development of wheat cultivars differing in vernalization response. Field Crops Res. 57 (1998) 289-300
30. Bagnall D.J. Light quality and vernalization interact in controlling late flowering in Arabidopsis ecotypes and mutants. Ann. Bot. 71 (1993) 75-83
31. Hempel F.D., and Feldman L.J. Bidirectional inflorescence development in Arabidopsis thaliana-acropetal initiation of flowers and basipetal initiation of paraclades. Planta 192 (1994) 276-286