The promoter of the Vicia faba L. leghemoglobin gene VfLb29 is specifically activated in the infected cells of root nodules and in the arbuscule-containing cells of mycorrhizal roots from different legume and nonlegume plants

Vieweg MF, Fruhling M, Quandt HJ, Heim U, Baumlein H, Pühler A, Küster H, Perlick AM (2004)
Mol Plant Microbe Interact 17(1): 62-69.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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DOI
Autor*in
Vieweg, MF; Fruhling, M; Quandt, HJ; Heim, U; Baumlein, H; Pühler, AlfredUniBi ; Küster, Helge; Perlick, AM
Einrichtung
Centrum für Biotechnologie > Arbeitsgruppe A. Pühler
Fakultät für Biologie
Centrum für Biotechnologie > Institut für Genomforschung und Systembiologie
Stichworte
root transformation
Erscheinungsjahr
2004
Zeitschriftentitel
Mol Plant Microbe Interact
Band
17
Ausgabe
1
Seite(n)
62-69
ISSN
0894-0282
Page URI
https://pub.uni-bielefeld.de/record/1608336

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Vieweg MF, Fruhling M, Quandt HJ, et al. The promoter of the Vicia faba L. leghemoglobin gene VfLb29 is specifically activated in the infected cells of root nodules and in the arbuscule-containing cells of mycorrhizal roots from different legume and nonlegume plants. Mol Plant Microbe Interact. 2004;17(1):62-69.
Vieweg, M. F., Fruhling, M., Quandt, H. J., Heim, U., Baumlein, H., Pühler, A., Küster, H., et al. (2004). The promoter of the Vicia faba L. leghemoglobin gene VfLb29 is specifically activated in the infected cells of root nodules and in the arbuscule-containing cells of mycorrhizal roots from different legume and nonlegume plants. Mol Plant Microbe Interact, 17(1), 62-69. https://doi.org/10.1094/MPMI.2004.17.1.62
Vieweg, MF, Fruhling, M, Quandt, HJ, Heim, U, Baumlein, H, Pühler, Alfred, Küster, Helge, and Perlick, AM. 2004. “The promoter of the Vicia faba L. leghemoglobin gene VfLb29 is specifically activated in the infected cells of root nodules and in the arbuscule-containing cells of mycorrhizal roots from different legume and nonlegume plants”. Mol Plant Microbe Interact 17 (1): 62-69.
Vieweg, M. F., Fruhling, M., Quandt, H. J., Heim, U., Baumlein, H., Pühler, A., Küster, H., and Perlick, A. M. (2004). The promoter of the Vicia faba L. leghemoglobin gene VfLb29 is specifically activated in the infected cells of root nodules and in the arbuscule-containing cells of mycorrhizal roots from different legume and nonlegume plants. Mol Plant Microbe Interact 17, 62-69.
Vieweg, M.F., et al., 2004. The promoter of the Vicia faba L. leghemoglobin gene VfLb29 is specifically activated in the infected cells of root nodules and in the arbuscule-containing cells of mycorrhizal roots from different legume and nonlegume plants. Mol Plant Microbe Interact, 17(1), p 62-69.
M.F. Vieweg, et al., “The promoter of the Vicia faba L. leghemoglobin gene VfLb29 is specifically activated in the infected cells of root nodules and in the arbuscule-containing cells of mycorrhizal roots from different legume and nonlegume plants”, Mol Plant Microbe Interact, vol. 17, 2004, pp. 62-69.
Vieweg, M.F., Fruhling, M., Quandt, H.J., Heim, U., Baumlein, H., Pühler, A., Küster, H., Perlick, A.M.: The promoter of the Vicia faba L. leghemoglobin gene VfLb29 is specifically activated in the infected cells of root nodules and in the arbuscule-containing cells of mycorrhizal roots from different legume and nonlegume plants. Mol Plant Microbe Interact. 17, 62-69 (2004).
Vieweg, MF, Fruhling, M, Quandt, HJ, Heim, U, Baumlein, H, Pühler, Alfred, Küster, Helge, and Perlick, AM. “The promoter of the Vicia faba L. leghemoglobin gene VfLb29 is specifically activated in the infected cells of root nodules and in the arbuscule-containing cells of mycorrhizal roots from different legume and nonlegume plants”. Mol Plant Microbe Interact 17.1 (2004): 62-69.

60 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Molecular identification of a root apical cell-specific and stress-responsive enhancer from an Arabidopsis enhancer trap line.
Zhang L, Qin LN, Zeng ZR, Wu CZ, Gong YY, Liu LH, Cao FQ., Plant Methods 15(), 2019
PMID: 30733820
Insights into the complex role of GRAS transcription factors in the arbuscular mycorrhiza symbiosis.
Hartmann RM, Schaepe S, Nübel D, Petersen AC, Bertolini M, Vasilev J, Küster H, Hohnjec N., Sci Rep 9(1), 2019
PMID: 30833646
Integrative Analysis of the Wheat PHT1 Gene Family Reveals A Novel Member Involved in Arbuscular Mycorrhizal Phosphate Transport and Immunity.
Zhang Y, Hu L, Yu D, Xu K, Zhang J, Li X, Wang P, Chen G, Liu Z, Peng C, Li C, Guo T., Cells 8(5), 2019
PMID: 31121904
The mycorrhiza-dependent defensin MtDefMd1 of Medicago truncatula acts during the late restructuring stages of arbuscule-containing cells.
Uhe M, Hogekamp C, Hartmann RM, Hohnjec N, Küster H., PLoS One 13(1), 2018
PMID: 29370287
Protocol: high-efficiency in-planta Agrobacterium-mediated transgenic hairy root induction of Camellia sinensis var. sinensis.
Alagarsamy K, Shamala LF, Wei S., Plant Methods 14(), 2018
PMID: 29483937
Cooperation and coexpression: How coexpression networks shift in response to multiple mutualists.
Palakurty SX, Stinchcombe JR, Afkhami ME., Mol Ecol 27(8), 2018
PMID: 29533484
Tomato CYCLOPS/IPD3 is required for mycorrhizal symbiosis but not tolerance to Fusarium wilt in mycorrhiza-deficient tomato mutant rmc.
Prihatna C, Larkan NJ, Barbetti MJ, Barker SJ., Mycorrhiza 28(5-6), 2018
PMID: 29948410
Comparative Expression Analysis of Rice and Arabidopsis Peroxiredoxin Genes Suggests Conserved or Diversified Roles Between the Two Species and Leads to the Identification of Tandemly Duplicated Rice Peroxiredoxin Genes Differentially Expressed in Seeds.
Gho YS, Park SA, Kim SR, Chandran AKN, An G, Jung KH., Rice (N Y) 10(1), 2017
PMID: 28647924
Efficient generation of mutations mediated by CRISPR/Cas9 in the hairy root transformation system of Brassica carinata.
Kirchner TW, Niehaus M, Debener T, Schenk MK, Herde M., PLoS One 12(9), 2017
PMID: 28937992
Fatty acid ω-hydroxylases from Solanum tuberosum.
Bjelica A, Haggitt ML, Woolfson KN, Lee DP, Makhzoum AB, Bernards MA., Plant Cell Rep 35(12), 2016
PMID: 27565479
OsEXPB2, a β-expansin gene, is involved in rice root system architecture
Zou H, Wenwen Y, Zang G, Kang Z, Zhang Z, Huang J, Wang G., Mol Breed 35(1), 2015
PMID: IND601201642
Responses of rose RhACS1 and RhACS2 promoters to abiotic stresses in transgenic Arabidopsis thaliana.
Khan MA, Meng Y, Liu D, Tang H, Lü S, Imtiaz M, Jiang G, Lü P, Ji Y, Gao J, Ma N., Plant Cell Rep 34(5), 2015
PMID: 25596927
Polymorphisms in the AOX2 gene are associated with the rooting ability of olive cuttings.
Hedayati V, Mousavi A, Razavi K, Cultrera N, Alagna F, Mariotti R, Hosseini-Mazinani M, Baldoni L., Plant Cell Rep 34(7), 2015
PMID: 25749737
MtZR1, a PRAF protein, is involved in the development of roots and symbiotic root nodules in Medicago truncatula.
Hopkins J, Pierre O, Kazmierczak T, Gruber V, Frugier F, Clement M, Frendo P, Herouart D, Boncompagni E., Plant Cell Environ 37(3), 2014
PMID: 23961805
Molecular cloning and characterization of a cassava translationally controlled tumor protein gene potentially related to salt stress response.
Santa Brígida AB, dos Reis SP, Costa Cde N, Cardoso CM, Lima AM, de Souza CR., Mol Biol Rep 41(3), 2014
PMID: 24413992
Involvement of papain and legumain proteinase in the senescence process of Medicago truncatula nodules.
Pierre O, Hopkins J, Combier M, Baldacci F, Engler G, Brouquisse R, Hérouart D, Boncompagni E., New Phytol 202(3), 2014
PMID: 24527680
Composite potato plants with transgenic roots on non-transgenic shoots: a model system for studying gene silencing in roots.
Horn P, Santala J, Nielsen SL, Hühns M, Broer I, Valkonen JP., Plant Cell Rep 33(12), 2014
PMID: 25182479
Temporal and spatial control of gene expression in horticultural crops.
Dutt M, Dhekney SA, Soriano L, Kandel R, Grosser JW., Hortic Res 1(), 2014
PMID: 26504550
Expression level of a flavonoid 3'-hydroxylase gene determines pathogen-induced color variation in sorghum.
Mizuno H, Yazawa T, Kasuga S, Sawada Y, Ogata J, Ando T, Kanamori H, Yonemaru J, Wu J, Hirai MY, Matsumoto T, Kawahigashi H., BMC Res Notes 7(), 2014
PMID: 25346182
The cis-acting CTTC-P1BS module is indicative for gene function of LjVTI12, a Qb-SNARE protein gene that is required for arbuscule formation in Lotus japonicus.
Lota F, Wegmüller S, Buer B, Sato S, Bräutigam A, Hanf B, Bucher M., Plant J 74(2), 2013
PMID: 23452278
An organ-specific role for ethylene in rose petal expansion during dehydration and rehydration.
Liu D, Liu X, Meng Y, Sun C, Tang H, Jiang Y, Khan MA, Xue J, Ma N, Gao J., J Exp Bot 64(8), 2013
PMID: 23599274
Role of protein farnesylation events in the ABA-mediated regulation of the Pinoresinol-Lariciresinol Reductase 1 (LuPLR1) gene expression and lignan biosynthesis in flax (Linum usitatissimum L.).
Corbin C, Decourtil C, Marosevic D, Bailly M, Lopez T, Renouard S, Doussot J, Dutilleul C, Auguin D, Giglioli-Guivarc'h N, Lainé E, Lamblin F, Hano C., Plant Physiol Biochem 72(), 2013
PMID: 23816064
A cytochrome P450 regulates a domestication trait in cultivated tomato.
Chakrabarti M, Zhang N, Sauvage C, Muños S, Blanca J, Cañizares J, Diez MJ, Schneider R, Mazourek M, McClead J, Causse M, van der Knaap E., Proc Natl Acad Sci U S A 110(42), 2013
PMID: 24082112
A sweetpotato SRD1 promoter confers strong root-, taproot-, and tuber-specific expression in Arabidopsis, carrot, and potato.
Noh SA, Lee HS, Huh GH, Oh MJ, Paek KH, Shin JS, Bae JM., Transgenic Res 21(2), 2012
PMID: 21660481
Two novel positive cis-regulatory elements involved in green tissue-specific promoter activity in rice (Oryza sativa L ssp.).
Ye R, Zhou F, Lin Y., Plant Cell Rep 31(7), 2012
PMID: 22388917
Screening of tissue-specific genes and promoters in tomato by comparing genome wide expression profiles of Arabidopsis orthologues.
Lim CJ, Lee HY, Kim WB, Lee BS, Kim J, Ahmad R, Kim HA, Yi SY, Hur CG, Kwon SY., Mol Cells 34(1), 2012
PMID: 22699756
Characterization of a set of novel meiotically-active promoters in Arabidopsis.
Li J, Farmer AD, Lindquist IE, Dukowic-Schulze S, Mudge J, Li T, Retzel EF, Chen C., BMC Plant Biol 12(), 2012
PMID: 22776406
Nitric oxide (NO): a key player in the senescence of Medicago truncatula root nodules.
Cam Y, Pierre O, Boncompagni E, Hérouart D, Meilhoc E, Bruand C., New Phytol 196(2), 2012
PMID: 22937888
The non-specific lipid transfer protein N5 of Medicago truncatula is implicated in epidermal stages of rhizobium-host interaction.
Pii Y, Molesini B, Masiero S, Pandolfini T., BMC Plant Biol 12(), 2012
PMID: 23217154
Identification of two conserved cis-acting elements, MYCS and P1BS, involved in the regulation of mycorrhiza-activated phosphate transporters in eudicot species.
Chen A, Gu M, Sun S, Zhu L, Hong S, Xu G., New Phytol 189(4), 2011
PMID: 21106037
Both plant and bacterial nitrate reductases contribute to nitric oxide production in Medicago truncatula nitrogen-fixing nodules.
Horchani F, Prévot M, Boscari A, Evangelisti E, Meilhoc E, Bruand C, Raymond P, Boncompagni E, Aschi-Smiti S, Puppo A, Brouquisse R., Plant Physiol 155(2), 2011
PMID: 21139086
Laser microdissection unravels cell-type-specific transcription in arbuscular mycorrhizal roots, including CAAT-box transcription factor gene expression correlating with fungal contact and spread.
Hogekamp C, Arndt D, Pereira PA, Becker JD, Hohnjec N, Küster H., Plant Physiol 157(4), 2011
PMID: 22034628
Rapid in planta evaluation of root expressed transgenes in chimeric soybean plants.
Li J, Todd TC, Trick HN., Plant Cell Rep 29(2), 2010
PMID: 20012965
Model legumes contribute to faba bean breeding
Rispail Nicolas, Kaló Péter, Kiss GyörgyB, Ellis THNoel, Gallardo Karine, Thompson RichardD, Prats Elena, Larrainzar Estibaliz, Ladrera Ruben, González EstherM, Arrese-Igor Cesar, Ferguson BrettJ, Gresshoff PeterM, Rubiales Diego., Field Crops Res 115(3), 2010
PMID: IND44316555
Promoters of the barley germin-like GER4 gene cluster enable strong transgene expression in response to pathogen attack.
Himmelbach A, Liu L, Zierold U, Altschmied L, Maucher H, Beier F, Müller D, Hensel G, Heise A, Schützendübel A, Kumlehn J, Schweizer P., Plant Cell 22(3), 2010
PMID: 20305123
The signal peptide of the Medicago truncatula modular nodulin MtNOD25 operates as an address label for the specific targeting of proteins to nitrogen-fixing symbiosomes.
Hohnjec N, Lenz F, Fehlberg V, Vieweg MF, Baier MC, Hause B, Küster H., Mol Plant Microbe Interact 22(1), 2009
PMID: 19061403
Composite Medicago truncatula plants harbouring Agrobacterium rhizogenes-transformed roots reveal normal mycorrhization by Glomus intraradices.
Mrosk C, Forner S, Hause G, Küster H, Kopka J, Hause B., J Exp Bot 60(13), 2009
PMID: 19574251
Metabolite profiling of mycorrhizal roots of Medicago truncatula.
Schliemann W, Ammer C, Strack D., Phytochemistry 69(1), 2008
PMID: 17706732
Heterologous expression of IAP1, a seed protein from bean modified by indole-3-acetic acid, in Arabidopsis thaliana and Medicago truncatula.
Walz A, Seidel C, Rusak G, Park S, Cohen JD, Ludwig-Müller J., Planta 227(5), 2008
PMID: 18097685
Molecular cloning, characterization and regulation of two different NADH-glutamate synthase cDNAs in bean nodules.
Blanco L, Reddy PM, Silvente S, Bucciarelli B, Khandual S, Alvarado-Affantranger X, Sánchez F, Miller S, Vance C, Lara-Flores M., Plant Cell Environ 31(4), 2008
PMID: 18182018
A transgenic dTph1 insertional mutagenesis system for forward genetics in mycorrhizal phosphate transport of Petunia.
Wegmüller S, Svistoonoff S, Reinhardt D, Stuurman J, Amrhein N, Bucher M., Plant J 54(6), 2008
PMID: 18315538
Evidence for sugar signalling in the regulation of asparagine synthetase gene expressed in Phaseolus vulgaris roots and nodules.
Silvente S, Reddy PM, Khandual S, Blanco L, Alvarado-Affantranger X, Sanchez F, Lara-Flores M., J Exp Bot 59(6), 2008
PMID: 18407964
Two ABREs, two redundant root-specific and one W-box cis-acting elements are functional in the sunflower HAHB4 promoter.
Manavella PA, Dezar CA, Ariel FD, Chan RL., Plant Physiol Biochem 46(10), 2008
PMID: 18586510
Knock-down of the MEP pathway isogene 1-deoxy-D-xylulose 5-phosphate synthase 2 inhibits formation of arbuscular mycorrhiza-induced apocarotenoids, and abolishes normal expression of mycorrhiza-specific plant marker genes.
Floss DS, Hause B, Lange PR, Küster H, Strack D, Walter MH., Plant J 56(1), 2008
PMID: 18557838
Functional biology of plant phosphate uptake at root and mycorrhiza interfaces.
Bucher M., New Phytol 173(1), 2007
PMID: 17176390
Arbuscular mycorrhizal fungi reduce the construction of extrafloral nectaries in Vicia faba.
Laird RA, Addicott JF., Oecologia 152(3), 2007
PMID: 17356811
Regulation of arbuscular mycorrhization by carbon. The symbiotic interaction cannot be improved by increased carbon availability accomplished by root-specifically enhanced invertase activity.
Schaarschmidt S, González MC, Roitsch T, Strack D, Sonnewald U, Hause B., Plant Physiol 143(4), 2007
PMID: 17416641
Transcriptome analysis of arbuscular mycorrhizal roots during development of the prepenetration apparatus.
Siciliano V, Genre A, Balestrini R, Cappellazzo G, deWit PJ, Bonfante P., Plant Physiol 144(3), 2007
PMID: 17468219
A rice promoter containing both novel positive and negative cis-elements for regulation of green tissue-specific gene expression in transgenic plants.
Cai M, Wei J, Li X, Xu C, Wang S., Plant Biotechnol J 5(5), 2007
PMID: 17596180
Transcriptional snapshots provide insights into the molecular basis of arbuscular mycorrhiza in the model legume Medicago truncatula.
Hohnjec N, Henckel K, Bekel T, Gouzy J, Dondrup M, Goesmann A, Kuster H., Functional plant biology : FPB. 33(8), 2006
PMID: IND43838506
Expression of SK3-type dehydrin in transporting organs is associated with cold acclimation in Solanum species.
Rorat T, Szabala BM, Grygorowicz WJ, Wojtowicz B, Yin Z, Rey P., Planta 224(1), 2006
PMID: 16404580
Two genes encoding different truncated hemoglobins are regulated during root nodule and arbuscular mycorrhiza symbioses of Medicago truncatula.
Vieweg MF, Hohnjec N, Küster H., Planta 220(5), 2005
PMID: 15517353
Signaling in the arbuscular mycorrhizal symbiosis.
Harrison MJ., Annu Rev Microbiol 59(), 2005
PMID: 16153162
Legume haemoglobins: symbiotic nitrogen fixation needs bloody nodules.
Downie JA., Curr Biol 15(6), 2005
PMID: 15797009
The mycorrhizal fungus Gigaspora margarita possesses a CuZn superoxide dismutase that is up-regulated during symbiosis with legume hosts.
Lanfranco L, Novero M, Bonfante P., Plant Physiol 137(4), 2005
PMID: 15749992
Overlaps in the transcriptional profiles of Medicago truncatula roots inoculated with two different Glomus fungi provide insights into the genetic program activated during arbuscular mycorrhiza.
Hohnjec N, Vieweg MF, Pühler A, Becker A, Küster H., Plant Physiol 137(4), 2005
PMID: 15778460
Combined transcriptome profiling reveals a novel family of arbuscular mycorrhizal-specific Medicago truncatula lectin genes.
Frenzel A, Manthey K, Perlick AM, Meyer F, Pühler A, Küster H, Krajinski F., Mol Plant Microbe Interact 18(8), 2005
PMID: 16134889
Suppression of allene oxide cyclase in hairy roots of Medicago truncatula reduces jasmonate levels and the degree of mycorrhization with Glomus intraradices.
Isayenkov S, Mrosk C, Stenzel I, Strack D, Hause B., Plant Physiol 139(3), 2005
PMID: 16244141
MtENOD11 gene activation during rhizobial infection and mycorrhizal arbuscule development requires a common AT-rich-containing regulatory sequence.
Boisson-Dernier A, Andriankaja A, Chabaud M, Niebel A, Journet EP, Barker DG, de Carvalho-Niebel F., Mol Plant Microbe Interact 18(12), 2005
PMID: 16478046
Transcriptome profiling in root nodules and arbuscular mycorrhiza identifies a collection of novel genes induced during Medicago truncatula root endosymbioses.
Manthey K, Krajinski F, Hohnjec N, Firnhaber C, Pühler A, Perlick AM, Küster H., Mol Plant Microbe Interact 17(10), 2004
PMID: 15497399

38 References

Daten bereitgestellt von Europe PubMed Central.

Hydrogen peroxide accumulation in Medicago truncatula roots colonized by the arbuscular mycorrhiza-forming fungus Glomus intraradices
Salzer, Planta 208(3), 1999
Nitric oxide in plants. To NO or not to NO.
Wojtaszek P., Phytochemistry 54(1), 2000
PMID: 10846738
Defense gene induction in tobacco by nitric oxide, cyclic GMP, and cyclic ADP-ribose.
Durner J, Wendehenne D, Klessig DF., Proc. Natl. Acad. Sci. U.S.A. 95(17), 1998
PMID: 9707647
Plant Cell Responses to Arbuscular Mycorrhizal Fungi: Getting to the Roots of the Symbiosis.
Gianinazzi-Pearson V., Plant Cell 8(10), 1996
PMID: 12239368
A promoter for strong and ubiquitous anaerobic gene expression in tobacco
Kohler, The Plant Journal 10(1), 1996
Synchronous expression of leghaemoglobin genes in Medicago truncatula during nitrogen-fixing root nodule development and response to exogenously supplied nitrate.
Gallusci P, Dedieu A, Journet EP, Huguet T, Barker DG., Plant Mol. Biol. 17(3), 1991
PMID: 1883994
The Vicia faba leghemoglobin gene VfLb29 is induced in root nodules and in roots colonized by the arbuscular mycorrhizal fungus Glomus fasciculatum.
Fruhling M, Roussel H, Gianinazzi-Pearson V, Puhler A, Perlick AM., Mol. Plant Microbe Interact. 10(1), 1997
PMID: 9002275
Nod factor-induced expression of leghemoglobin to study the mechanism of NH4NO3 inhibition on root hair deformation.
Heidstra R, Nilsen G, Martinez-Abarca F, van Kammen A, Bisseling T., Mol. Plant Microbe Interact. 10(2), 1997
PMID: 9057327
Soybean (lbc3), Parasponia, and Trema Hemoglobin Gene Promoters Retain Symbiotic and Nonsymbiotic Specificity in Transgenic Casuarinaceae: Implications for Hemoglobin Gene Evolution and Root Nodule Symbioses
Franche, Molecular Plant-Microbe Interactions 11(9), 1998
Agrobacterium rhizogenes-transformed roots of Medicago truncatula for the study of nitrogen-fixing and endomycorrhizal symbiotic associations.
Boisson-Dernier A, Chabaud M, Garcia F, Becard G, Rosenberg C, Barker DG., Mol. Plant Microbe Interact. 14(6), 2001
PMID: 11386364
Medicago truncatula ENOD11: a novel RPRP-encoding early nodulin gene expressed during mycorrhization in arbuscule-containing cells.
Journet EP, El-Gachtouli N, Vernoud V, de Billy F, Pichon M, Dedieu A, Arnould C, Morandi D, Barker DG, Gianinazzi-Pearson V., Mol. Plant Microbe Interact. 14(6), 2001
PMID: 11386369
Reactive oxygen species, nitric oxide and glutathione: a key role in the establishment of the legume–Rhizobium symbiosis?
Hérouart, Plant Physiology and Biochemistry 40(6-8), 2002
Cross walls in arbuscular trunk hyphae form after loss of metabolic activity.
Dickson S, Smith SE., New Phytol. 151(3), 2001
PMID: IND23236754
A new hemoglobin gene from soybean: a role for hemoglobin in all plants.
Anderson CR, Jensen EO, LLewellyn DJ, Dennis ES, Peacock WJ., Proc. Natl. Acad. Sci. U.S.A. 93(12), 1996
PMID: 8650152
Two hemoglobin genes in Arabidopsis thaliana: the evolutionary origins of leghemoglobins.
Trevaskis B, Watts RA, Andersson CR, Llewellyn DJ, Hargrove MS, Olson JS, Dennis ES, Peacock WJ., Proc. Natl. Acad. Sci. U.S.A. 94(22), 1997
PMID: 9342391
A hemoglobin from plants homologous to truncated hemoglobins of microorganisms.
Watts RA, Hunt PW, Hvitved AN, Hargrove MS, Peacock WJ, Dennis ES., Proc. Natl. Acad. Sci. U.S.A. 98(18), 2001
PMID: 11526234
Expression of early nodulin genes in alfalfa mycorrhizae indicates that signal transduction pathways used in forming arbuscular mycorrhizae and Rhizobium-induced nodules may be conserved.
van Rhijn P, Fang Y, Galili S, Shaul O, Atzmon N, Wininger S, Eshed Y, Lum M, Li Y, To V, Fujishige N, Kapulnik Y, Hirsch AM., Proc. Natl. Acad. Sci. U.S.A. 94(10), 1997
PMID: 11038545
Cell-specific expression of the promoters of two nonlegume hemoglobin genes in a transgenic legume, Lotus corniculatus.
Andersson CR, Llewellyn DJ, Peacock WJ, Dennis ES., Plant Physiol. 113(1), 1997
PMID: 9008386
Plant hemoglobins
Arredondo-Peter R, Hargrove MS, Moran JF, Sarath G, Klucas RV., Plant Physiol. 118(4), 1998
PMID: 9847086
Symbiotic and nonsymbiotic hemoglobin genes of Casuarina glauca.
Jacobsen-Lyon K, Jensen EO, Jorgensen JE, Marcker KA, Peacock WJ, Dennis ES., Plant Cell 7(2), 1995
PMID: 7756831
MOLECULAR AND CELLULAR ASPECTS OF THE ARBUSCULAR MYCORRHIZAL SYMBIOSIS.
Harrison MJ., Annu. Rev. Plant Physiol. Plant Mol. Biol. 50(), 1999
PMID: 15012214
Hemoglobin genes in non-legumes: cloning and characterization of a Casuarina glauca hemoglobin gene.
Christensen T, Dennis ES, Peacock JW, Landsmann J, Marcker KA., Plant Mol. Biol. 16(2), 1991
PMID: 1893106
Use of Mycorrhizae in Agriculture
Jeffries, Critical Reviews in Biotechnology 5(4), 1987
A new method for observing the morphology of vesicular-arbuscular mycorrhizae
Brundrett, Botany 62(10), 1984
Expression and evolution of functionally distinct haemoglobin genes in plants.
Hunt PW, Watts RA, Trevaskis B, Llewelyn DJ, Burnell J, Dennis ES, Peacock WJ., Plant Mol. Biol. 47(5), 2001
PMID: 11725952
A phosphate transporter expressed in arbuscule-containing cells in potato.
Rausch C, Daram P, Brunner S, Jansa J, Laloi M, Leggewie G, Amrhein N, Bucher M., Nature 414(6862), 2001
PMID: 11719809
Nitric oxide functions as a signal in plant disease resistance.
Delledonne M, Xia Y, Dixon RA, Lamb C., Nature 394(6693), 1998
PMID: 9707120
Local Induction of a Mycorrhiza-Specific Class III Chitinase Gene in Cortical Root Cells of Medicago truncatula Containing Developing or Mature Arbuscules
Bonanomi, Plant Biology 3(2), 2001
What are hemoglobins doing in plants?
Hill, Botany 76(5), 1998
Developmental genetics and evolution of symbiotic structures in nitrogen-fixing nodules and arbuscular mycorrhiza.
Provorov NA, Borisov AY, Tikhonovich IA., J. Theor. Biol. 214(2), 2002
PMID: 11812174
A phosphate transporter from Medicago truncatula involved in the acquisition of phosphate released by arbuscular mycorrhizal fungi.
Harrison MJ, Dewbre GR, Liu J., Plant Cell 14(10), 2002
PMID: 12368495
Targeted inoculation of Medicago truncatula in vitro root cultures reveals MtENOD11 expression during early stages of infection by arbuscular mycorrhizal fungi.
Chabaud M, Venard C, Defaux-Petras A, Becard G, Barker DG., New Phytol. 156(2), 2002
PMID: IND23302762
Expression of symbiotic and nonsymbiotic globin genes responding to microsymbionts on Lotus japonicus.
Uchiumi T, Shimoda Y, Tsuruta T, Mukoyoshi Y, Suzuki A, Senoo K, Sato S, Kato T, Tabata S, Higashi S, Abe M., Plant Cell Physiol. 43(11), 2002
PMID: 12461135
First report of non-mycorrhizal plant mutants (Myc−) obtained in pea (Pisum sativum L.) and fababean (Vicia faba L.)
DUC, Plant Science 60(2), 1989
Primary structure and promoter analysis of leghemoglobin genes of the stem-nodulated tropical legume Sesbania rostrata: conserved coding sequences, cis-elements and trans-acting factors.
Metz BA, Welters P, Hoffmann HJ, Jensen EO, Schell J, de Bruijn FJ., Mol. Gen. Genet. 214(2), 1988
PMID: 3237206
The promoter of the Vicia faba L. VfENOD-GRP3 gene encoding a glycine-rich early nodulin mediates a predominant gene expression in the interzone II-III region of transgenic Vicia hirsuta root nodules.
Kuster H, Quandt HJ, Broer I, Perlick AM, Puhler A., Plant Mol. Biol. 29(4), 1995
PMID: 8541502
NewAgrobacterium helper plasmids for gene transfer to plants
Hood, Transgenic Research 2(4), 1993
Oxygen and the regulation of nitrogen fixation in legume nodules
Layzell, Physiologia Plantarum 80(2), 1990
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