Pyramiding resistances based on translation initiation factors in Arabidopsis is impaired by male gametophyte lethality

Plant Signaling and Behavior

Volumn 9, Issue FEB, 2014, Pages

  Callot, Caroline ^a   Gallois, Jean Luc ^a  

^a CEMAGREF   (France)

Author keywords

Arabidopsis; eIF4E; Gametophyte development; Translation initiation; Virus resistance

Indexed keywords

ARABIDOPSIS PROTEIN; INITIATION FACTOR; TRANSCRIPTOME;

ALLELE; ARABIDOPSIS; CROSS BREEDING; DISEASE RESISTANCE; GENE EXPRESSION REGULATION; GENETICS; GENOTYPING TECHNIQUE; IMMUNOLOGY; METABOLISM; MUTATION; PHYSIOLOGY; PLANT DISEASE; PLANT GENE; POLLEN;

ALLELES; ARABIDOPSIS; ARABIDOPSIS PROTEINS; CROSSES, GENETIC; DISEASE RESISTANCE; GENE EXPRESSION REGULATION, PLANT; GENES, PLANT; GENOTYPING TECHNIQUES; MUTATION; PEPTIDE INITIATION FACTORS; PLANT DISEASES; POLLEN; TRANSCRIPTOME;

ARABIDOPSIS; ARABIDOPSIS THALIANA; EUKARYOTA;

EID: 84898731498     PISSN: 15592316     EISSN: 15592324     Source Type: Journal    
DOI: 10.4161/psb.27940     Document Type: Article

References (26)

1. Hernández G, Altmann M, Lasko P. Origins and evolution of the mechanisms regulating translation initiation in eukaryotes. Trends Biochem Sci 2010; 35:63-73;PMID:19926289; http://dx.doi.org/10.1016/j.tibs.2009.10.009
2. Altmann M, Handschin C, Trachsel H. mRNA cap-binding protein: cloning of the gene encoding protein synthesis initiation factor eIF-4E from Saccharomyces cerevisiae. Mol Cell Biol 1987; 7:998-1003;PMID:3550438
3. Brenner C, Nakayama N, Goebl M, Tanaka K, Toh-e A, Matsumoto K. CDC33 encodes mRNA cap-binding protein eIF-4E of Saccharomyces cerevisiae. Mol Cell Biol 1988; 8:3556-9;PMID:3062383
4. Patrick RM, Browning KS. The eIF4F and eIFiso4F Complexes of Plants: An Evolutionary Perspective. Comp Funct Genomics 2012; 2012:287814.
5. Lellis AD, Allen ML, Aertker AW, Tran JK, Hillis DM, Harbin CR, Caldwell C, Gallie DR, Browning KS. Deletion of the eIFiso4G subunit of the Arabidopsis eIFiso4F translation initiation complex impairs health and viability. Plant Mol Biol 2010; 74:249-63;PMID:20694742; http://dx.doi.org/10.1007/s11103-010-9670-z
6. Robaglia C, Caranta C. Translation initiation factors: a weak link in plant RNA virus infection. Trends Plant Sci 2006; 11:40-5;PMID:16343979; http://dx.doi.org/10.1016/j.tplants.2005.11.004
7. Ruud KA, Kuhlow C, Goss DJ, Browning KS. Identification and characterization of a novel cap-binding protein from Arabidopsis thaliana. J Biol Chem 1998; 273:10325-30;PMID:9553087; http://dx.doi.org/10.1074/jbc.273.17.10325
8. Duprat A, Caranta C, Revers F, Menand B, Browning KS, Robaglia C. The Arabidopsis eukaryotic initiation factor (iso)4E is dispensable for plant growth but required for susceptibility to potyviruses. Plant J 2002; 32:927-34;PMID:12492835; http://dx.doi.org/10.1046/j.1365-313X.2002.01481.x
9. Nicaise V, Gallois JL, Chafiai F, Allen LM, Schurdi-Levraud V, Browning KS, Candresse T, Caranta C, Le Gall O, German-Retana S. Coordinated and selective recruitment of eIF4E and eIF4G factors for potyvirus infection in Arabidopsis thaliana. FEBS Lett 2007; 581:1041-6;PMID:17316629; http://dx.doi.org/10.1016/j.febslet.2007.02.007
10. Yoshii M, Nishikiori M, Tomita K, Yoshioka N, Kozuka R, Naito S, Ishikawa M. The Arabidopsis cucumovirus multiplication 1 and 2 loci encode translation initiation factors 4E and 4G. J Virol 2004; 78:6102-11;PMID:15163703; http://dx.doi.org/10.1128/JVI.78.12.6102-6111.2004
11. Mazier M, Flamain F, Nicolaï M, Sarnette V, Caranta C. Knock-down of both eIF4E1 and eIF4E2 genes confers broad-spectrum resistance against potyviruses in tomato. PLoS One 2011; 6:e29595;PMID:22242134; http://dx.doi.org/10.1371/journal.pone.0029595
12. Combe JP, Petracek ME, van Eldik G, Meulewaeter F, Twell D. Translation initiation factors eIF4E and eIFiso4E are required for polysome formation and regulate plant growth in tobacco. Plant Mol Biol 2005; 57:749-60;PMID:15988567; http://dx.doi.org/10.1007/s11103-005-3098-x
13. Wang A, Krishnaswamy S. Eukaryotic translation initiation factor 4E-mediated recessive resistance to plant viruses and its utility in crop improvement. Mol Plant Pathol 2012; 13:795-803;PMID:22379950; http://dx.doi.org/10.1111/j.1364-3703.2012.00791.x
14. Sato M, Nakahara K, Yoshii M, Ishikawa M, Uyeda I. Selective involvement of members of the eukaryotic initiation factor 4E family in the infection of Arabidopsis thaliana by potyviruses. FEBS Lett 2005; 579:1167-71;PMID:15710407; http://dx.doi.org/10.1016/j.febslet.2004.12.086
15. Gallois JL, Charron C, Sánchez F, Pagny G, Houvenaghel MC, Moretti A, Ponz F, Revers F, Caranta C, German-Retana S. Single amino acid changes in the turnip mosaic virus viral genome-linked protein (VPg) confer virulence towards Arabidopsis thaliana mutants knocked out for eukaryotic initiation factors eIF(iso)4E and eIF(iso)4G. J Gen Virol 2010; 91:288-93;PMID:19741065; http://dx.doi.org/10.1099/vir.0.015321-0
16. Reinbold C, Lacombe S, Ziegler-Graff V, Scheidecker D, Wiss L, Beuve M, Caranta C, Brault V. Closely related poleroviruses depend on distinct translation initiation factors to infect Arabidopsis thaliana. Mol Plant Microbe Interact 2013; 26:257-65;PMID:23013438; http://dx.doi.org/10.1094/MPMI-07-12-0174-R
17. Boavida LC, Becker JD, Feijó JA. The making of gametes in higher plants. Int J Dev Biol 2005; 49:595-614;PMID:16096968; http://dx.doi.org/10.1387/ijdb.052019lb
18. Page DR, Grossniklaus U. The art and design of genetic screens: Arabidopsis thaliana. Nat Rev Genet 2002; 3:124-36;PMID:11836506; http://dx.doi.org/10.1038/nrg730
19. Bonhomme S, Horlow C, Vezon D, de Laissardière S, Guyon A, Férault M, Marchand M, Bechtold N, Pelletier G. T-DNA mediated disruption of essential gametophytic genes in Arabidopsis is unexpectedly rare and cannot be inferred from segregation distortion alone. Mol Gen Genet 1998; 260:444-52;PMID:9894914; http://dx.doi.org/10.1007/s004380050915
20. Gallois JL, Guyon-Debast A, Lécureuil A, Vezon D, Carpentier V, Bonhomme S, Guerche P. The Arabidopsis proteasome RPT5 subunits are essential for gametophyte development and show accession-dependent redundancy. Plant Cell 2009; 21:442-59;PMID:19223514; http://dx.doi.org/10.1105/tpc.108.062372
21. Honys D, Twell D. Transcriptome analysis of haploid male gametophyte development in Arabidopsis. Genome Biol 2004; 5:R85;PMID:15535861; http://dx.doi.org/10.1186/gb-2004-5-11-r85
22. Alexander MP. Differential staining of aborted and nonaborted pollen. Stain Technol 1969; 44:117-22;PMID:4181665
23. Peterson R, Slovin JP, Chen C. A simplified method for differential staining of aborted and non-aborted pollen grains. Int J Plant Biol 2010; 1:e13; http://dx.doi.org/10.4081/pb.2010.e13
24. Dai S, Chen T, Chong K, Xue Y, Liu S, Wang T. Proteomics identification of differentially expressed proteins associated with pollen germination and tube growth reveals characteristics of germinated Oryza sativa pollen. Mol Cell Proteomics 2007; 6:207-30;PMID:17132620; http://dx.doi.org/10.1074/mcp.M600146-MCP200
25. Charron C, Nicolaï M, Gallois JL, Robaglia C, Moury B, Palloix A, Caranta C. Natural variation and functional analyses provide evidence for co-evolution between plant eIF4E and potyviral VPg. Plant J 2008; 54:56-68;PMID:18182024; http://dx.doi.org/10.1111/j.1365-313X.2008.03407.x
26. Piron F, Nicolaï M, Minoïa S, Piednoir E, Moretti A, Salgues A, Zamir D, Caranta C, Bendahmane A. An induced mutation in tomato eIF4E leads to immunity to two potyviruses. PLoS One 2010; 5:e11313;PMID:20593023; http://dx.doi.org/10.1371/journal.pone.0011313