Corrigendum: Suppression of B function strongly supports the modified ABCE model in Tricyrtis sp. (Liliaceae) (Scientific Reports (2017) 6 (24549) DOI: 10.1038/srep24549);Suppression of B function strongly supports the modified ABCE model in Tricyrtis sp. (Liliaceae)

Scientific Reports

Volumn 6, Issue , 2016, Pages

  Otani, Masahiro ^a   Sharifi, Ahmad ^b   Kubota, Shosei ^c,d,e   Oizumi, Kanako ^c   Uetake, Fumi ^c   Hirai, Masayo ^c   Hoshino, Yoichiro ^f   Kanno, Akira ^c   Nakano, Masaru ^a  

^a NIIGATA UNIVERSITY   (Japan)

^b AVICENNA RESEARCH INSTITUTE   (Iran)

^c TOHOKU UNIVERSITY   (Japan)

^d UNIVERSITY OF TOKYO   (Japan)

^e NIHON UNIVERSITY   (Japan)

^f HOKKAIDO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

GENE INACTIVATION; GENE SILENCING; IDENTITY; LILIACEAE; MODEL; ORGAN; OVULE; REPRESSOR GENE; SPECIES; STAMEN; STIGMA; TRANSGENIC PLANT; BIOLOGICAL MODEL; FLOWER; GENE EXPRESSION REGULATION; GENETICS; PHYLOGENY; PLANT GENE; REAL TIME POLYMERASE CHAIN REACTION; SCANNING ELECTRON MICROSCOPY;

FLOWERS; GENE EXPRESSION REGULATION, PLANT; GENES, PLANT; LILIACEAE; MICROSCOPY, ELECTRON, SCANNING; MODELS, GENETIC; PHYLOGENY; PLANTS, GENETICALLY MODIFIED; REAL-TIME POLYMERASE CHAIN REACTION;

EID: 84964258844     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep42322     Document Type: Erratum

References (45)

1. Bowman, J. L., Smyth, D. R. & Meyerowitz, E. M. Genetic interactions among floral homeotic genes of Arabidopsis. Development 112, 1-20 (1991).
2. Coen, E. S. & Meyerowitz, E. M. The war of the whorls: genetic interactions controlling flower development. Nature 353, 31-37 (1991).
3. Goto, K. & Meyerowitz, E. M. Function and regulation of the Arabidopsis floral homeotic gene PISTILLATA. Genes Dev. 8, 1548-1560 (1994).
4. Riechmann, J. L., Krizek, B. A. & Meyerowitz, E. M. Dimerization specificity of Arabidopsis MADS domain homeotic proteins APETALA1, APETALA3, PISTILLATA, and AGAMOUS. Proc. Natl. Acad. Sci. USA 93, 4793-4798 (1996).
5. Kim, S. et al. Phylogeny and diversification of B-function MADS-box genes in angiosperms: evolutionary and functional implications of a 260-million-year-old duplication. Am. J. Bot. 9, 2102-2118 (2004).
6. Hernández-Hernández, T., Martínez-Castilla, L. P. & Alvarez-Buylla, E. R. Functional diversification of B MADS-box homeotic regulators of flower development: Adaptive evolution in protein-protein interaction domains after major gene duplication events. Mol. Biol. Evol. 24, 465-481 (2007).
7. de Martino, G. et al. Functional analyses of two tomato APETALA3 genes demonstrate diversification in their roles in regulating floral development. Plant Cell 18, 1833-1845 (2006).
8. Geuten, K. & Irish, V. Hidden variability of floral homeotic B genes in Solanaceae provides a molecular basis for the evolution of novel functions. Plant Cell 22, 2562-2578 (2010).
9. Sharma, B. & Kramer, E. Sub- and neo-functionalization of APETALA3 paralogs have contributed to the evolution of novel floral organ identity in Aquilegia (columbine, Ranunculaceae). New Phytol. 197, 949-957 (2013).
10. Zhang, J. S. et al. Deciphering the Physalis floridana Double-Layered-Lantern1 mutant provides insights into functional divergence of the GLOBOSA duplicates within the Solanaceae. Plant Physiol. 164, 748-764 (2014).
11. Pelaz, S. et al. B and C floral organ identity functions require SEPALLATA MADS-box genes. Nature 405, 200-203 (2000).
12. Ditta, G. et al. The SEP4 gene of Arabidopsis thaliana functions in floral organ and meristem identity. Curr. Biol. 14, 1935-1940 (2004).
13. Van Tunen, A. J., Eikelboom, W. & Angenent, G. C. Floral organogenesis in Tulipa. Flowering Newslett. 16, 33-37 (1993).
14. Tzeng, T. Y. & Yang, C. H. A MADS box gene from lily (Lilium longiflorum) is sufficient to generate dominant negative mutation by interacting with PISTILLATA (PI) In Arabidopsis thaliana. Plant Cell Physiol. 42, 1156-1168 (2001).
15. Kanno, A. et al. Heterotopic expression of class B floral homeotic genes supports a modified ABC model for tulip (Tulipa gesneriana). Plant Mol. Biol. 52, 831-841 (2003).
16. Nakamura, T. et al. The modified ABC model explains the development of the petaloid perianth of Agapanthus praecox ssp. orientalis (Agapanthaceae) flowers. Plant Mol. Biol. 58, 435-445 (2005).
17. Nakada, M. et al. Isolation of MaDEF from Muscari armeniacum and analysis of its expression using laser microdissection. Plant Sci. 170, 143-150 (2006).
18. Xu, Y. et al. Floral organ identity genes in the orchid Dendrobium crumenatum. Plant J. 46, 54-68 (2006).
19. Tsaftaris, A., Polidoros, A. N., Pasentsis, K. & Kalivas, A. Tepal formation and expression pattern of B-class paleoAP3-like MADSbox genes in crocus (Crocus sativus L.). Plant Sci. 170, 238-246 (2006).
20. Hirai, M., Kamimura, T. & Kanno, A. The expression patterns of three class B genes in two distinctive whorls of petaloid tepals in Alstroemeria ligtu. Plant Cell Physiol. 48, 310-321 (2007).
21. Hirai, M., Ochiai, T. & Kanno, A. The expression of two DEFICIENS-like genes was reduced in the sepaloid tepals of viridiflora tulips. Breed. Sci. 60, 110-120 (2010).
22. Su, C. L. et al. A modified ABCDE model of flowering in orchids based on gene expression profiling studies of the moth orchid Phalaenopsis aphrodite. Plos ONE 8, e80462 (2013).
23. Bowman, J. L., Smyth, D. R. & Meyerowitz, E. M. Genes directing flower development in Arabidopsis. Plant Cell 1, 37-52 (1989).
24. Tröbner, W. et al. GLOBOSA: a homeotic gene which interacts with DEFICIENS in the control of Antirrhinum floral organogenesis. EMBO J. 11, 4693-4704 (1992).
25. Angenent, G. C. et al. Petal and stamen formation in petunia is regulated by the homeotic gene fbp1. Plant J. 4, 101-112 (1993).
26. Lange, M. et al. The seirena B class floral homeotic mutant of California Poppy (Eschscholzia californica) reveals a function of the enigmatic PI motif in the formation of specific multimeric MADS domain protein complexes. Plant Cell 25, 438-53 (2013).
27. Benlloch, R. et al. Analysis of B function in legumes: PISTILLATA proteins do not require the PI motif for floral organ development in Medicago truncatula. Plant J. 60, 102-111 (2009).
28. Yan, X. et al. Functional identification and characterization of the Brassica napus transcription factor gene BnAP2, the ortholog of Arabidopsis thaliana APETALA2. Plos ONE 7, e33890 (2012).
29. Roque, E. et al. Functional specialization of duplicated AP3-like genes in Medicago truncatula. Plant J. 73, 663-675 (2013).
30. Adachi, Y., Mori, S. & Nakano, M. Agrobacterium-mediated production of transgenic plants in Tricyrtis hirta (Liliaceae). Acta Hort. 673, 415-419 (2004).
31. Mori, S. et al. Stability of β-glucuronidase gene expression in transgenic Tricyrtis hirta plants after two years of cultivation. Biol. Plant 52, 513-516 (2008).
32. Hiei, Y., Ohta, S., Komari, T. & Kumashiro, T. Efficient transformation of rice (Oryza sativa L.) mediated by Agrobacterium and sequence analysis of the boundaries of the T-DNA. Plant J. 6, 271-282 (1994).
33. Kim, S. et al. Expression of floral MADS-box genes in basal angiosperms: implications for the evolution of floral regulators. Plant J. 43, 724-744 (2005).
34. Guo, X. et al. The tomato floral homeotic protein FBP1-like gene, SlGLO1, plays key roles in petal and stamen development. Sci. Rep. 6, 20454 (2016).
35. van Doorn, W. G. & Van Meeteren, U. Flower opening and closure: a review. J. Exp. Bot. 54, 1801-1812 (2003).
36. Vandenbussche, M. et al. The duplicated B-class heterodimer model: whorl-specific effects and complex genetic interactions in Petunia hybrida flower development. Plant Cell 16, 741-754 (2004).
37. Manchado-Rojo, M. et al. Quantitative levels of Deficiens and Globosa during late petal development show a complex transcriptional network topology of B function. Plant J. 72, 294-307 (2012).
38. Nakano, M. et al. Somatic embryogenesis and plant regeneration from callus cultures of several species in the genus Tricyrtis. In Vitro Cell Dev. Biol. Plant 40, 274-278 (2004).
39. Frohman, M. A., Dush, M. K. & Martin, G. R. Rapid production of full length cDNAs from rare transcripts: Amplification using a single gene specific oligonucleotide primer. Proc. Natl Acad. Sci. USA 85, 8998-9002 (1988).
40. Tamura, K. et al. MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0. Mol. Biol. Evol. 30, 2725-2729 (2013).
41. Kamiishi, Y. et al. Flower color alteration in the liliaceous ornamental Tricyrtis sp. by RNA interference-mediated suppression of the chalcone synthase gene. Mol. Breed. 30, 671-680 (2012).
42. Ririe, K., M. Rasmussen, R. P. & Wittwer, C. T. Product differentiation by analysis of DNA melting curves during the polymerase chain reaction. Anal. Biochem. 245, 154-160 (1997).
43. Ohta, M. et al. Repression domains of class II ERF transcriptional repressors share an essential motif for active repression. Plant Cell 13, 1959-1968 (2001).
44. Koike, Y., Hoshino, Y., Mii, M. & Nakano, M. Horticultural characterization of Angelonia salicariifolia plants transformed with wildtype strains of Agrobacterium rhizogenes. Plant Cell Rep. 21, 981-987 (2003).
45. Nonaka, T. et al. Chromosome doubling of Lychnis spp. by in vitro spindle toxin treatment of nodal segments. Sci. Hort. 129, 832-839 (2011).