Plant hemoglobin participation in cell fate determination

Plant Signaling and Behavior

Volumn 9, Issue JUN, 2014, Pages

  Huang, Shuanglong ^a   Hill, Robert D ^a   Stasolla, Claudio ^a  

^a UNIVERSITY OF MANITOBA   (Canada)

Author keywords

Cell fate; Embryogenesis; Hemoglobin; Hormone; Nitric oxide

Indexed keywords

ZEA MAYS;

HEMOGLOBIN; INDOLEACETIC ACID DERIVATIVE; NITRIC OXIDE; PHYTOHORMONE; PLANT PROTEIN;

APOPTOSIS; CELL DIFFERENTIATION; EMBRYOLOGY; GENE EXPRESSION REGULATION; GROWTH, DEVELOPMENT AND AGING; MAIZE; METABOLISM; PHYSIOLOGICAL STRESS; PLANT DEVELOPMENT; PLANT SEED;

APOPTOSIS; CELL DIFFERENTIATION; GENE EXPRESSION REGULATION, PLANT; HEMOGLOBINS; INDOLEACETIC ACIDS; NITRIC OXIDE; PLANT DEVELOPMENT; PLANT GROWTH REGULATORS; PLANT PROTEINS; SEEDS; STRESS, PHYSIOLOGICAL; ZEA MAYS;

EID: 84924267377     PISSN: 15592316     EISSN: 15592324     Source Type: Journal    
DOI: 10.4161/psb.29485     Document Type: Article

References (33)

1. Thorpe TA, Stasolla C. Somatic embryogenesis. Current Trends in the Embryology of Angiosperms. Bhojwani SS, Soh WY, eds. Dordrecht: Kluwer Academic Publisher, 2001:279-336
2. Chugh A, Khurana P. Gene expression during somatic embryogenesis: recent advances. Curr Sci 2002; 83:715-30
3. Thibaud-Nissen F, Shealy RT, Khanna A, Vodkin LO. Clustering of microarray data reveals transcript patterns associated with somatic embryogenesis in soybean. Plant Physiol 2003; 132:118-36; PMID:12746518; http://dx.doi.org/10.1104/pp.103.019968
4. Feher A, Pasternak TP, Dudits D. Transition of somatic plant cells to an embryogenic state. Plant Cell Tissue Organ Cult 2003; 74:201-28; http://dx.doi.org/10.1023/A:1024033216561
5. Zeng F, Zhang X, Zhu L, Tu L, Guo X, Nie Y. Isolation and characterization of genes associated to cotton somatic embryogenesis by suppression subtractive hybridization and macroarray. Plant Mol Biol 2006; 60:167-83; PMID:16429258; http://dx.doi.org/10.1007/s11103-005-3381-x
6. Karlova R, Boeren S, Russinova E, Aker J, Vervoort J, de Vries S. The Arabidopsis SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE1 protein complex includes BRASSINOSTEROIDINSENSITIVE1. Plant Cell 2006; 18:626-38; PMID:16473966; http://dx.doi.org/10.1105/tpc.105.039412
7. Müller B, Sheen J. Cytokinin and auxin interaction in root stem-cell specification during early embryogenesis. Nature 2008; 453:1094-7; PMID:18463635; http://dx.doi.org/10.1038/nature06943
8. Iwase A, Mitsuda N, Koyama T, Hiratsu K, Kojima M, Arai T, Inoue Y, Seki M, Sakakibara H, Sugimoto K, et al. The AP2/ERF transcription factor WIND1 controls cell dedifferentiation in Arabidopsis. Curr Biol 2011; 21:508-14; PMID:21396822; http://dx.doi.org/10.1016/j.cub.2011.02.020
9. Otvös K, Pasternak TP, Miskolczi P, Domoki M, Dorjgotov D, Szucs A, Bottka S, Dudits D, Fehér A. Nitric oxide is required for, and promotes auxinmediated activation of, cell division and embryogenic cell formation but does not influence cell cycle progression in alfalfa cell cultures. Plant J 2005; 43:849-60; PMID:16146524; http://dx.doi. org/10.1111/j.1365-313X.2005.02494.x
10. Dordas C, Hasinoff BB, Igamberdiev AU, Manac'h N, Rivoal J, Hill RD. Expression of a stress-induced hemoglobin affects NO levels produced by alfalfa root cultures under hypoxic stress. Plant J 2003; 35:763-70; PMID:12969429; http://dx.doi. org/10.1046/j.1365-313X.2003.01846.x
11. Smagghe BJ, Blervacq AS, Blassiau C, Decottignies JP, Jacquot JP, Hargrove MS, Hilbert JL. Immunolocalization of non-symbiotic hemoglobins during somatic embryogenesis in chicory. PlantSign. Behav. 2007; 2:43-9
12. Parent C, Berger A, Folzer H, Dat J, Crevècoeur M, Badot PM, Capelli N. A novel nonsymbiotic hemoglobin from oak: cellular and tissue specificity of gene expression. New Phytol 2008; 177:142-54; PMID:17986182
13. Bustos-Sanmamed P, Tovar-Méndez A, Crespi M, Sato S, Tabata S, Becana M. Regulation of nonsymbiotic and truncated hemoglobin genes of Lotus japonicus in plant organs and in response to nitric oxide and hormones. New Phytol 2011; 189:765-76; PMID:21073469; http://dx.doi. org/10.1111/j.1469-8137.2010.03527.x
14. Leiva-Eriksson N, Pin PA, Kraft T, Dohm JC, Minoche AE, Himmelbauer H, Bülow L. Differential expression patterns of non-symbiotic hemoglobins in sugar beet (Beta vulgaris ssp. vulgaris). Plant Cell Physiol 2014; 55:834-44; PMID:24486763; http://dx.doi.org/10.1093/pcp/pcu027
15. Dumont E, Jokipii-Lukkari S, Parkash V, Vuosku J, Sundström R, Nymalm Y, Sutela S, Taskinen K, Kallio PT, Salminen TA, et al. Evolution, three-dimensional model and localization of truncated hemoglobin PttTrHb of hybrid aspen. PLoS One 2014; 9:e88573; PMID:24520401; http://dx.doi.org/10.1371/journal. pone.0088573
16. Elhiti M, Hebelstrup KH, Wang A, Li C, Cui Y, Hill RD, Stasolla C. Function of type-2 Arabidopsis hemoglobin in the auxin-mediated formation of embryogenic cells during morphogenesis. Plant J 2013; 74:946-58; PMID:23510449; http://dx.doi. org/10.1111/tpj.12181
17. Hill RD. Non-symbiotic haemoglobins-What's happening beyond nitric oxide scavenging? AoB Plants 2012.
18. Huang S, Hill RD, Wally OS, Dionisio G, Ayele BT, Jami SK, Stasolla C. Hemoglobin control of cell survival/death decision regulates in vitro plant embryogenesis. Plant Physiol 2014; 165:810-25; http://dx.doi.org/10.1104/pp.114.239335; PMID:24784758
19. Freschi L. Nitric oxide and phytohormone interactions: current status and perspectives. Front Plant Sci 2013; 4:398; PMID:24130567; http://dx.doi. org/10.3389/fpls.2013.00398
20. Yu M, Lamattina L, Spoel SH, Loake GJ. Nitric oxide function in plant biology: a redox cue in deconvolution. New Phytol 2014; 202:1142-56; PMID:24611485; http://dx.doi.org/10.1111/nph.12739
21. Jenik PD, Gillmor CS, Lukowitz W. Embryonic patterning in Arabidopsis thaliana. Annu Rev Cell Dev Biol 2007; 23:207-36; PMID:17539754; h t t p: / / d x. d o i. o r g / 1 0. 114 6 / a n n u r e v. cellbio.22.011105.102609
22. Möller B, Weijers D. Auxin control of embryo patterning. Cold Spring Harb Perspect Biol 2009; 1:a001545; PMID:20066117; http://dx.doi. org/10.1101/cshperspect.a001545
23. Michniewicz M, Zago MK, Abas L, Weijers D, Schweighofer A, Meskiene I, Heisler MG, Ohno C, Zhang J, Huang F, et al. Antagonistic regulation of PIN phosphorylation by PP2A and PINOID directs auxin flux. Cell 2007; 130:1044-56; PMID:17889649; http://dx.doi.org/10.1016/j. cell.2007.07.033
24. Kawashima T, Goldberg RB. The suspensor: not just suspending the embryo. Trends Plant Sci 2010; 15:23-30; PMID:19963427; http://dx.doi. org/10.1016/j.tplants.2009.11.002
25. Vanstraelen M, Benková E. Hormonal interactions in the regulation of plant development. Annu Rev Cell Dev Biol 2012; 28:463-87; PMID:22856461; http://dx.doi.org/10.1146/annurev-cellbio-101011-155741
26. Rademacher EH, Lokerse AS, Schlereth A, Llavata-Peris CI, Bayer M, Kientz M, Freire Rios A, Borst JW, Lukowitz W, Jürgens G, et al. Different auxin response machineries control distinct cell fates in the early plant embryo. Dev Cell 2012; 22:211-22; PMID:22264733; http://dx.doi.org/10.1016/j. devcel.2011.10.026
27. Dombrecht B, Xue GP, Sprague SJ, Kirkegaard JA, Ross JJ, Reid JB, Fitt GP, Sewelam N, Schenk PM, Manners JM, et al. MYC2 differentially modulates diverse jasmonate-dependent functions in Arabidopsis. Plant Cell 2007; 19:2225-45; PMID:17616737; http://dx.doi.org/10.1105/tpc.106.048017
28. Kazan K, Manners JM. MYC2: the master in action. Mol Plant 2013; 6:686-703; PMID:23142764; http://dx.doi.org/10.1093/mp/sss128
29. Xia QZ, Zhang XL, Nie YC, Guo XP. [Withdrawal of exogenous auxin induces programmed cell death of cotton embryogenic suspension cultures]. Zhi Wu Sheng Li Yu Fen Zi Sheng Wu Xue Xue Bao 2005; 31:78-84; PMID:15692182
30. Manac'h-Little N, Igamberdiev AU, Hill RD. Hemoglobin expression affects ethylene production in maize cell cultures. Plant Physiol Biochem 2005; 43:485-9; PMID:15914016; http://dx.doi. org/10.1016/j.plaphy.2005.03.012
31. Wang Y, Elhiti M, Hebelstrup KH, Hill RD, Stasolla C. Manipulation of hemoglobin expression affects Arabidopsis shoot organogenesis. Plant Physiol Biochem 2011; 49:1108-16; PMID:21741261; http://dx.doi.org/10.1016/j.plaphy.2011.06.005
32. Hill RD, Huang S, Stasolla C. Hemoglobins, programmed cell death and somatic embryogenesis. Plant Sci 2013; 211:35-41; PMID:23987809; http://dx.doi.org/10.1016/j.plantsci.2013.06.010
33. Mur LA, Sivakumaran A, Mandon J, Cristescu SM, Harren FJ, Hebelstrup KH. Haemoglobin modulates salicylate and jasmonate/ethylene-mediated resistance mechanisms against pathogens. J Exp Bot 2012; 63:4375-87; PMID:22641422; http://dx.doi. org/10.1093/jxb/ers116