Antagonistic Action of Yucasine and DMSO on Apogamy in the Fern Dryopteris affinis ssp. affinis

  1. Sánchez, Eugenio
  2. Menéndez, Alejandro
  3. Rivera, Alejandro
  4. Cañal, María Jesús
  5. Fernández, Helena
  1. 1 Universidad de Oviedo
    info

    Universidad de Oviedo

    Oviedo, España

    ROR https://ror.org/006gksa02

Libro:
Ferns

ISBN: 9789811661693 9789811661709

Año de publicación: 2022

Páginas: 309-323

Tipo: Capítulo de Libro

DOI: 10.1007/978-981-16-6170-9_14 GOOGLE SCHOLAR lock_openAcceso abierto editor

Resumen

Apogamy is a peculiar case of apomixis, very frequent in ferns, in which an asexual embryo evolves from somatic cells of the gametophyte generation. This work reports about the effect of the yucasine, an inhibitor of the auxin biosynthesis, on vegetative and reproductive development of the gametophyte of Dryopteris affinis ssp. affinis, an obligate apogamous species. To cope with it, homogenized gametophytes were cultured in vitro in liquid Murashige and Skoog medium, supplemented with sucrose 2% (w/v), and tested up to three concentrations of yucasine (0.47, 4.7, and 23.6 μM). This compound was dissolved using dimethyl sulfoxide (DMSO), and therefore a control with the maximum dose (0.5%) used of this agent was included in the experiment.

Referencias bibliográficas

  • Asker SE, Jerling L (1992) Apomixis in plants. CRC Press, Boca Ratón. ISBN 978-0-8493-4545-6
  • Berleth T, Sachs T (2001) Plant morphogenesis: long-distance coordination and local patterning. Curr Opin Plant Biol 4(1):57–62
  • Casanova-Sáez R, Voß U (2019) Auxin metabolism controls developmental decisions in land plants. Trends Plant Sci 24(8):741–754
  • Chen X, Lai HG, Sun Q, Liu JP, Chen SB, Zhu WL (2018) Induction of apomixis by dimethyl sulfoxide (DMSO) and genetic identification of apomictic plants in cassava. Breed Sci 68(2):227–232. https://doi.org/10.1270/jsbbs.17089
  • Cheng Y, Dai X, Zhao Y (2007) Auxin synthesized by the YUCCA flavin monooxygenases is essential for embryogenesis and leaf formation in Arabidopsis. Plant Cell 19(8):2430–2439
  • Dai X, Mashiguchi K, Chen Q, Kasahara H, Kamiya Y, Ojha S, DuBois J, Ballou D, Zhao Y (2013) The biochemical mechanism of auxin biosynthesis by an Arabidopsis YUCCA flavin-containing monooxygenase. J Biol Chem 288(3):1448–1457
  • Davies PJ (ed) (2010) Plant hormones: biosynthesis, signal transduction, action. Springer, Dordrecht, p 802. ISBN 978-1-4020-2684-3
  • Dyer RJ, Savolainen V, Schneider H (2012) Apomixis and reticulate evolution in the Asplenium monanthes fern complex. Ann Bot 110(8):1515–1529
  • Ekrt L, Koutecký P (2015) Between sexual and apomictic: unexpectedly variable sporogenesis and production of viable polyhaploids in the pentaploid fern of the Dryopteris affinis agg. (Dryopteridaceae). Ann Bot 117(1):97–106
  • Fei X, Shi J, Liu Y, Niu J, Wei A (2019) The steps from sexual reproduction to apomixis. Planta 249(6):1715–1730
  • Fernández H and Revilla MA. (2003). In vitro culture of ornamental ferns. Plant Cell Tissue Organ Cult 73, 1–13
  • Fraser-Jenkins CR (1980) Dryopteris affinis: a new treatment for a complex species in the European Pteridophyte Flora, vol 10. Botanischer Garten und Botanisches Museum, Berlin
  • Fujino K, Matsuda Y, Ozawa K, Nishimura T, Koshiba T, Fraaije MW, Sekiguchi H (2008) NARROW LEAF 7 controls LEAF shape mediated by auxin in rice. Mol Genet Genomics 279(5):499–507
  • Gallavotti A, Barazesh S, Malcomber S, Hall D, Jackson D, Schmidt RJ, McSteen P (2008) Sparse inflorescence1 encodes a monocot-specific YUCCA-like gene required for vegetative and reproductive development in maize. PNAS 105(39):15196–15201
  • Grossmann J, Fernández H, Chaubey PM, Valdés AE, Gagliardini V, Cañal MJ, Russo G, Grossniklaus U (2017) Proteogenomic analysis greatly expands the identification of proteins related to reproduction in the apogamous fern Dryopteris affinis ssp affinis. Front Plant Sci. 8:336
  • Grossniklaus U, Koltunow AM, Van Lookeren M (1998) A bright future for apomixis. Trends Plant Sci 3:415–416
  • Grusz AL (2016) A current perspective on apomixis in ferns. J Syst Evol 54:656–665
  • Kandemir N, Saygili I (2015) Apomixis: new horizons in plant breeding. Turk J Agric For 39:549–556
  • Koltunow AM, Grossniklaus U (2003) Apomixis: a developmental perspective. Ann Rev Plant Biol 54(1):547–574
  • Limera C, Wang K, Xu L, Wang Y, Zhu X, Feng H, Sha Y, Gong Y, Liu L (2016) Induction of autotetraploidy using colchicine and its identification in radish (Raphanus sativus L.). J Hortic Sci Biotechnol 91:63–70
  • Liu HM, Dyer RJ, Guo ZY, Meng Z, Li JH, Schneider H (2012) The evolutionary dynamics of apomixis in ferns: a case study from Polystichoid ferns. J Bot:510478. https://doi.org/10.1155/2012/510478
  • Lovis JD (1978) Evolutionary patterns and processes in ferns. Adv Bot Res 4(January):229–415
  • Mashiguchi K, Tanaka K, Sakai T, Sugawara S, Kawaide H, Natsume M, Hanada A, Yaeno T, Shirasu K, Yao H, McSteen P, Zhao Y, Hayashi K, Kamiya Y, Kasahara H (2011) The main auxin biosynthesis pathway in Arabidopsis. PNAS 108(45):18512–18517
  • Menéndez V, Villacorta NF, Revilla MA, Gotor V, Bernard P, Fernández H (2006) Exogenous and endogenous growth regulators on apogamy in Dryopteris affinis (Lowe) Fraser-Jenkins sp. affinis. Plant Cell Rep 25(2):85–91
  • Mikuła A, Pożoga M, Tomiczak K, Rybczyński JJ (2015) Somatic embryogenesis in ferns: a new experimental system. Plant Cell Rep 34:783–794
  • Murashige T, Skoog F (1962) A revised medium for rapid growth and bioassays with tobacco tissue cultures. Plant Physiol. 15:473–497
  • Nishimura T, Hayash KI, Suzuki H, Gyohda A, Takaoka C, Sakaguchi Y, Matsumoto S, Kasahara H, Sakai T, Kato JI, Kamiya Y, Koshiba T (2014) Yucasin is a potent inhibitor of YUCCA, a key enzyme in auxin biosynthesis. Plant J 77(3):352–366
  • Ozias-Akins P (2006) Apomixis: developmental characteristics and genetics. Crit Rev Plant Sci 25:199–214
  • Pacifici E, Polverari L, Sabatini S (2015) Plant hormone cross-talk: the pivot of root growth. J Exp Bot 66:1113–1121
  • Somer M, Arbesú R, Menéndez V, Revilla MA, Fernández H (2010) Sporophyte induction studies in ferns in vitro. Euphytica 171(2):203–210
  • Stepanova AN, Robertson-Hoyt J, Yun J, Benavente LM, Xie DY, Doležal K, Schlereth A, Jürgens G, Alonso JM (2008) TAA1-mediated auxin biosynthesis is essential for hormone crosstalk and plant development. Cell 133(1):177–191
  • Tao Y, Ferrer JJ, Ljung K, Pojer F, Hong F, Long JA, Li L, Moreno JE, Bowman ME, Ivans LJ, Cheng Y, Lim J, Zhao Y, Ballaré CL, Sandberg G, Noel JP, Chory J (2008) Rapid synthesis of auxin via a new tryptophan-dependent pathway is required for shade avoidance in plants. Cell 133(1):164–176
  • Team Rs (2016) RStudio: integrated development for R. RStudio, Boston
  • Thao NTP, Ureshino K, Miyajima I, Ozaki Y, Okubo H (2003) Induction of tetraploids in ornamental Alocasia through colchicine and oryzalin treatments. Plant Cell Tissue Organ Cult 72:19–25. https://doi.org/10.1023/A:1021292928295
  • Thimann KV (1977) Hormone action in the whole life of plants. The University of Massachusetts Press, Amherst, p 464. ISBN 978-0870232244
  • Tucker MR, Araujo ACG, Paech NA, Hecht V, Schmidt EDL, Rossell JB, De Vries SC, Koltunow AMG (2003) Sexual and apomictic reproduction in Hieracium subgenus Pilosella are closely interrelated developmental pathways. Plant Cell 15:152437
  • White RA (1979) Experimental investigations of fern sporophyte development. BioSci 21(6):271–275
  • Won C, Shen X, Mashiguchi K, Zheng Z, Dai X, Cheng Y, Kasahara H, Kamiya Y, Chory J, Zhao Y (2011) Conversion of tryptophan to indole-3-acetic acid by TRYPTOPHAN AMINOTRANSFERASES OF ARABIDOPSIS and YUCCAs in Arabidopsis. PNAS 108(45):18518–18523
  • Woodward AW, Bartel B (2005) Auxin: regulation, action, and interaction. Ann Bot 95(5):707–735
  • Wyder S, Rivera A, Valdés AE, Cañal MJ, Gagliardini V, Fernández H, Grossniklaus U (2020) Differential gene expression profiling of one- and two-dimensional apogamous gametophytes of the fern Dryopteris affinis ssp. affinis. Plant Physiol Biochem 148(January):302–311
  • Yamada M, Greenham K, Prigge MJ, Jensen PJ, Estelle M (2009) The TRANSPORT INHIBITOR RESPONSE2 gene is required for auxin synthesis and diverse aspects of plant development. Plant Physiol 151(1):168–179
  • Yamamoto Y, Kamiya N, Morinaka Y, Matsuoka M, Sazuka T (2007) Auxin biosynthesis by the YUCCA genes in Rice. Plant Physiol 143(3):1362–1371
  • Zhao Z, Gu MG (1984) Production of diploid pure lines of maize through parthenogenesis induced by chemicals. Acta Genet Sin 11:39–46