Differential expression profiles of poplar MAP kinase kinases in response to abiotic stresses and plant hormones, and overexpression of PtMKK4 improves the drought tolerance of poplar

Gene

Volumn 545, Issue 1, 2014, Pages 141-148

  Wang, Lei ^a   Su, Hongyan ^a   Han, Liya ^a   Wang, Chuanqi ^a   Sun, Yanlin ^a   Liu, Fenghong ^a  

^a LUDONG UNIVERSITY   (China)

Author keywords

Abiotic stresses; MAPKK; Poplar; PtMKK4; Signal molecules

Indexed keywords

HYDROGEN PEROXIDE; MITOGEN ACTIVATED PROTEIN KINASE KINASE 4; PHYTOHORMONE; PTDREB8 PROTEIN; PTLTP3 PROTEIN; PTP5CS PROTEIN; PTSUS3 PROTEIN; UNCLASSIFIED DRUG; VEGETABLE PROTEIN; ANTIOXIDANT; GENETIC MARKER; MITOGEN ACTIVATED PROTEIN KINASE KINASE;

ABIOTIC STRESS; ARTICLE; CONTROLLED STUDY; DROUGHT TOLERANCE; GENE EXPRESSION PROFILING; GENE OVEREXPRESSION; GENETIC ANALYSIS; MARKER GENE; MULTIGENE FAMILY; NONHUMAN; PLANT GENE; POPULUS TRICHOCARPA; PRIORITY JOURNAL; PROTEIN FUNCTION; SIGNAL TRANSDUCTION; TRANSGENE; WILD TYPE; DROUGHT; GENE EXPRESSION REGULATION; GENETIC MARKER; GENETICS; METABOLISM; OXIDATIVE STRESS; PHYSIOLOGICAL STRESS; PHYSIOLOGY; POPULUS; SALINITY; TRANSGENIC PLANT;

POPULUS TRICHOCARPA;

ANTIOXIDANTS; DROUGHTS; GENE EXPRESSION REGULATION, PLANT; GENETIC MARKERS; MITOGEN-ACTIVATED PROTEIN KINASE KINASES; OXIDATIVE STRESS; PLANT GROWTH REGULATORS; PLANT PROTEINS; PLANTS, GENETICALLY MODIFIED; POPULUS; SALINITY; STRESS, PHYSIOLOGICAL;

EID: 84901237452     PISSN: 03781119     EISSN: 18790038     Source Type: Journal    
DOI: 10.1016/j.gene.2014.04.058     Document Type: Article

References (33)

1. Agrawal G.K., Iwahashi H., Rakwal R. Rice MAPKs. Biochemical and Biophysical Research Communications 2003, 302:171-180.
2. Andreasson E., Ellis B. Convergence and specificity in the Arabidopsis MAPK nexus. Trends in Plant Science 2010, 15:106-113.
3. Armengaud P., Thiery L., Buhot N., Grenier-de March G., Savouré A. Transcriptional regulation of proline biosynthesis in Medicago truncatula reveals developmental and environmental specific features. Physiologia Plantarum 2004, 120:442-450.
4. Asai T., et al. MAP kinase signalling cascade in Arabidopsis innate immunity. Nature 2002, 415:977-983.
5. Bates L., Waldren R., Teare I. Rapid determination of free proline for water stress studies. Plant and Soil 1973, 39:205-207.
6. Chyzhykova O., Palladina T. The role of amino acids and sugars in supporting of osmotic homeostasis in maize seedlings under salinization conditions and treatment with synthetic growth regulators. Ukrainskiǐ Biokhimicheskiǐ Zhurnal 2006, 78:124-129.
7. Cohen D., et al. Comparative transcriptomics of drought responses in Populus: a meta-analysis of genome-wide expression profiling in mature leaves and root apices across two genotypes. BMC Genomics 2010, 11:630.
8. Doczi R., et al. The Arabidopsis mitogen-activated protein kinase kinase MKK3 is upstream of group C mitogen-activated protein kinases and participates in pathogen signaling. Plant Cell 2007, 19:3266-3279.
9. Hamel L.P., et al. Activation of stress-responsive mitogen-activated protein kinase pathways in hybrid poplar (Populus trichocarpa×Populus deltoides). Tree Physiology 2005, 25:277-288.
10. Hamel L.P., et al. Ancient signals: comparative genomics of plant MAPK and MAPKK gene families. Trends in Plant Science 2006, 11:192-198.
11. Jiang M., Zhang J. Effect of abscisic acid on active oxygen species, antioxidative defence system and oxidative damage in leaves of maize seedlings. Plant & Cell Physiology 2001, 42:1265-1273.
12. Jonak C., Okresz L., Bogre L., Hirt H. Complexity, cross talk and integration of plant MAP kinase signalling. Current Opinion in Plant Biology 2002, 5:415-424.
13. Kong X., et al. ZmMKK4, a novel group C MAPK kinase in maize (Zea mays), confers salt and cold tolerance in transgenic Arabidopsis. Plant, Cell & Environment 2011, 34:1291-1303.
14. Liu J., Zhu J.K. Proline accumulation and salt-stress-induced gene expression in a salt-hypersensitive mutant of Arabidopsis. Plant Physiology 1997, 114:591-596.
15. Lu W., Chu X., Li Y., Wang C., Guo X. Cotton GhMKK1 induces the tolerance of salt and drought stress, and mediates defence responses to pathogen infection in transgenic Nicotiana benthamiana. PloS One 2013, 8:e68503.
16. Ma H.S., Liang D., Shuai P., Xia X.L., Yin W.L. The salt- and drought-inducible poplar GRAS protein SCL7 confers salt and drought tolerance in Arabidopsis thaliana. Journal of Experimental Botany 2010, 61:4011-4019.
17. MAPK Group Mitogen-activated protein kinase cascades in plants: a new nomenclature. Trends in Plant Science 2002, 7:301-308.
18. Nicole M.C., Hamel L.P., Morency M.J., Beaudoin N., Ellis B.E., Séguin A. MAP-ping genomic organization and organ-specific expression profiles of poplar MAP kinases and MAP kinase kinases. BMC Genomics 2006, 7:223.
19. Ning J., Li X., Hicks L.M., Xiong L. A Raf-like MAPKKK gene DSM1 mediates drought resistance through reactive oxygen species scavenging in rice. Plant Physiology 2010, 152:876-890.
20. Pan J., et al. ZmMPK17, a novel maize group D MAP kinase gene, is involved in multiple stress responses. Planta 2012, 235:661-676.
21. Rao K.P., Richa T., Kumar K., Raghuram B., Sinha A.K. In silico analysis reveals 75 members of mitogen-activated protein kinase kinase kinase gene family in rice. DNA Research 2010, 17:139-153.
22. Ren D., et al. A fungal-responsive MAPK cascade regulates phytoalexin biosynthesis in Arabidopsis. Proceedings of the National Academy of Sciences of the United States of America 2008, 105:5638-5643.
23. Rodriguez M.C., Petersen M., Mundy J. Mitogen-activated protein kinase signaling in plants. Annual Review of Plant Biology 2010, 61:621-649.
24. Šamajová O., Plíhal O., Al-Yousif M., Hirt H., Šamaj J. Improvement of stress tolerance in plants by genetic manipulation of mitogen-activated protein kinases. Biotechnology Advances 2013, 31:118-128.
25. Smékalová V., Doskočilová A., Komis G., Samaj J. Crosstalk between secondary messengers, hormones and MAPK modules during abiotic stress signalling in plants. Biotechnology Advances 2014, 32:2-11.
26. Takahashi F., et al. The mitogen-activated protein kinase cascade MKK3-MPK6 is an important part of the jasmonate signal transduction pathway in Arabidopsis. Plant Cell 2007, 19:805-818.
27. Takahashi F., Mizoguchi T., Yoshida R., Ichimura K., Shinozaki K. Calmodulin-dependent activation of MAP kinase for ROS homeostasis in Arabidopsis. Molecular Cell 2011, 41:649-660.
28. Tang S., et al. Populus euphratica: the transcriptomic response to drought stress. Plant Molecular Biology 2013, 83:539-557.
29. Teige M., et al. The MKK2 pathway mediates cold and salt stress signaling in Arabidopsis. Molecular Cell 2004, 15:141-152.
30. Tuteja N. Abscisic acid and abiotic stress signaling. Plant Signaling & Behavior 2007, 2:135-138.
31. Zhang M., et al. ZmMKK3, a novel maize group B mitogen-activated protein kinase kinase gene, mediates osmotic stress and ABA signal responses. Journal of Plant Physiology 2012, 169:1501-1510.
32. Zhou Z., Wang M.J., Zhao S.T., Hu J.J., Lu M.Z. Changes in freezing tolerance in hybrid poplar caused by up- and down-regulation of PtFAD2 gene expression. Transgenic Research 2010, 19:647-654.
33. Zong X.J., Li D.P., Gu L.K., Li D.Q., Liu L.X., Hu X.L. Abscisic acid and hydrogen peroxide induce a novel maize group C MAP kinase gene ZmMPK7, which is responsible for the removal of reactive oxygen species. Planta 2009, 229:485-495.