DOI QR코드

DOI QR Code

An ARIA-Interacting AP2 Domain Protein Is a Novel Component of ABA Signaling

  • Lee, Sun-ji (Department of Molecular Biotechnology and Kumho Life Science Laboratory, College of Agriculture and Life Sciences, Chonnam National University) ;
  • Cho, Dong-im (Department of Molecular Biotechnology and Kumho Life Science Laboratory, College of Agriculture and Life Sciences, Chonnam National University) ;
  • Kang, Jung-youn (Department of Molecular Biotechnology and Kumho Life Science Laboratory, College of Agriculture and Life Sciences, Chonnam National University) ;
  • Kim, Soo Young (Department of Molecular Biotechnology and Kumho Life Science Laboratory, College of Agriculture and Life Sciences, Chonnam National University)
  • 투고 : 2008.12.14
  • 심사 : 2009.01.21
  • 발행 : 2009.04.30

초록

ADAP is an AP2-domain protein that interacts with ARIA, which, in turn, interacts with ABF2, a bZIP class transcription factor. ABF2 regulates various aspects of the abscisic acid (ABA) response by controlling the expression of a subset of ABA-responsive genes. Our expression analyses indicate that ADAP is expressed in roots, emerging young leaves, and flowers. We found that adap knockout mutant lines germinate more efficiently than wild-type plants and that the mutant seedlings grow faster. This suggests that ADAP is involved in the regulation of germination and seedling growth. Both germination and post-germination growth of the knockout mutants were partially insensitive to ABA, which indicates that ADAP is required for a full ABA response. The survival rates for mutants from which water was withheld were low compared with those for wild-type plants. The result shows that ADAP is necessary for the response to stress induced by water deprivation. Together, our data indicate that ADAP is a positive regulator of the ABA response and is also involved in regulating seedling growth. The role of ADAP is similar to that of ARIA, which is also a positive regulator of the ABA response. It appears that ADAP acts through the same ABA response pathway as ARIA.

키워드

과제정보

연구 과제 주관 기관 : Ministry of Education, Science, and Technology of Korea, Chonnam National University, Korea Science and Engineering Foundation

참고문헌

  1. Aida, M., Beis, D., Heidstra, R., Willemsen, V., Blilou, I., Galinha, C., Nussaume, L., Noh, Y.S., Amasino, R., and Scheres, B. (2004). The PLETHORA genes mediate patterning of the Arabidopsis root stem cell niche. Cell 119, 109-120 https://doi.org/10.1016/j.cell.2004.09.018
  2. Bardwell, V.J., and Treisman, R. (1994). The POZ domain: a conserved protein interaction motif. Genes Dev. 8, 1664-1677 https://doi.org/10.1101/gad.8.14.1664
  3. Bechtold, N., and Pelletier, G. (1998). In planta Agrobacteriummediated transformation of adult Arabidopsis thaliana plants by vacuum infiltration. Methods Mol. Biol. 82, 259-266
  4. Boutilier, K., Offringa, R., Sharma, V.K., Kieft, H., Ouellet, T., Zhang, L., Hattori, J., Liu, C.M., van Lammeren, A.A., Miki, B.L., et al. (2002). Ectopic expression of BABY BOOM triggers a conversion from vegetative to embryonic growth. Plant Cell 14, 1737-1749 https://doi.org/10.1105/tpc.001941
  5. Busk, P.K., and Pages, M. (1998). Regulation of abscisic acid induced transcription. Plant Mol. Biol. 37, 425-435 https://doi.org/10.1023/A:1006058700720
  6. Cernac, A., and Benning, C. (2004). WRINKLED1 encodes an AP2/EREB domain protein involved in the control of storage compound biosynthesis in Arabidopsis. Plant J. 40, 575-585 https://doi.org/10.1111/j.1365-313X.2004.02235.x
  7. Cernac, A., Andre, C., Hoffmann-Benning, S., and Benning, C. (2006). WRI1 is required for seed germination and seedling establishment. Plant Physiol. 141, 745-757 https://doi.org/10.1104/pp.106.079574
  8. Chien, C.T., Bartel, P.L., Sternglanz, R., and Fields, S. (1991). The two-hybrid system: a method to identify and clone genes for proteins that interact with a protein of interest. Proc. Natl. Acad. Sci. USA 88, 9578-9582 https://doi.org/10.1073/pnas.88.21.9578
  9. Choi, H., Hong, J., Kang, J., and Kim, S.Y. (2000). ABFs, a family of ABA-responsive element binding factors. J. Biol. Chem. 21, 1723-1730 https://doi.org/10.1074/jbc.275.3.1723
  10. Choi, H., Park, H., Park, J., Kim, S., Im, M., Seo, H., Kim, Y., Hwang, I., and Kim, S.Y. (2005). Arabidopsis calcium-dependent protein kinase AtCPK32 interacts with ABF4, a transcriptional regulator of abscisic acid-responsive gene expression, and modulates its activity. Plant Physiol. 139, 1750-61 https://doi.org/10.1104/pp.105.069757
  11. Chuck, G., Meeley, R.B., and Hake, S. (1998). The control of maize spikelet meristem fate by the APETALA2-like gene indeterminate spikelet1. Genes Dev. 12, 1145-1154 https://doi.org/10.1101/gad.12.8.1145
  12. Collins, T., Stone, J.R., and Williams, A.J. (2001). All in the family: the BTB/POZ, KRAB, and SCAN domains. Mol. Cell. Biol. 21, 3609-3615 https://doi.org/10.1128/MCB.21.11.3609-3615.2001
  13. Elliott, R.C., Betzner, A.S., Huttner, E., Oakes, M.P., Tucker, W.Q., Gerentes, D., Perez, P., and Smyth, D.R. (1996). AINTEGUMENTA, an APETALA2-like gene of Arabidopsis with pleiotropic roles in ovule development and floral organ growth. Plant Cell 8, 155-168 https://doi.org/10.1105/tpc.8.2.155
  14. Finkelstein, R.R., Gampala, S.S., and Rock, C.D. (2002). Abscisic acid signaling in seeds and seedlings. Plant Cell 14, S15-S45 https://doi.org/10.1105/tpc.010441
  15. Foster, R., Izawa, T., and Chua, N.H. (1994). Plant bZIP proteins gather at ACGT elements. FASEB J. 8, 192-200 https://doi.org/10.1096/fasebj.8.2.8119490
  16. Hirayama, T., and Shinozaki, K. (2007). Perception and transduction of abscisic acid signals: keys to the function of the versatile plant hormone ABA. Trends Plant Sci. 14, 343-351 https://doi.org/10.1016/j.tplants.2007.06.013
  17. Jefferson, R.A., Kavanagh, T.A., and Bevan, M.W. (1987). GUS fusions: b-glucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J. 20, 3901-3907
  18. Jofuku, K.D., den Boer, B.G., Van Montagu, M., and Okamuro, J.K. (1994). Control of Arabidopsis flower and seed development by the homeotic gene APETALA2. Plant Cell 6, 1211-1225 https://doi.org/10.1105/tpc.6.9.1211
  19. Kang, J., Choi, H., Im, M., and Kim, S.Y. (2002). Arabidopsis basic leucine zipper proteins that mediate stress-responsive abscisic acid signaling. Plant Cell 14, 343-357 https://doi.org/10.1105/tpc.010362
  20. Kim, J.-B., Kang, J.-Y., and Kim, S.Y. (2004a). Over-expression of a transcription factor regulating ABA-responsive gene expression confers multiple stress tolerance. Plant Biotechnol. J. 2, 459-466 https://doi.org/10.1111/j.1467-7652.2004.00090.x
  21. Kim, S., Kang, J., Cho, D.-I., Park, J.H., and Kim, S.Y. (2004b). ABF2, an ABRE-Binding bZIP factor, is an essential component of glucose signaling and its overexpression affects multiple stress tolerance. Plant J. 40, 75-87 https://doi.org/10.1111/j.1365-313X.2004.02192.x
  22. Kim, S., Choi, H., Ryu, H., Park, J., Kim, M., and Kim, S.Y. (2004c). ARIA, an Arabidopsis arm repeat protein interacting with a transcriptional regulator of abscisic acid-responsive gene expression, is a novel abscisic acid signaling component. Plant Physiol. 136, 3639-3648 https://doi.org/10.1104/pp.104.049189
  23. Klucher, K.M., Chow, H., Reiser, L., and Fischer, R.L. (1996). The AINTEGUMENTA gene of Arabidopsis required for ovule and female gametophyte development is related to the floral homeotic gene APETALA2. Plant Cell 8, 137-153 https://doi.org/10.1105/tpc.8.2.137
  24. Landschulz, W.H., Johnson, P.F., and McKnight, S.L. (1988). The leucine zipper: a hypothetical structure common to a new class of DNA binding proteins. Science 240, 1759-1764 https://doi.org/10.1126/science.3289117
  25. Moose, S.P., and Sisco, P.H. (1996). Glossy15, an APETALA2-like gene from maize that regulates leaf epidermal cell identity. Genes Dev. 10, 3018-3027 https://doi.org/10.1101/gad.10.23.3018
  26. Murashige, T., and Skoog, F. (1962). A revised medium for rapid growth and bioassay with tobacco tissue culture. Physiol. Plant. 15, 473-497 https://doi.org/10.1111/j.1399-3054.1962.tb08052.x
  27. Nakano, T., Suzuki, K., Fujimura, T., and Shinshi, H. (2006). Genome-wide analysis of the ERF gene family in Arabidopsis and rice. Plant Physiol. 140, 411-432 https://doi.org/10.1104/pp.105.073783
  28. Pandey, G.K., Grant, J.J., Cheong, Y.H., Kim, B.G., Li, L., and Luan, S. (2005). ABR1, an APETALA2-domain transcription factor that functions as a repressor of ABA response in Arabidopsis. Plant Physiol. 139, 1185-1193 https://doi.org/10.1104/pp.105.066324
  29. Sakuma, Y., Liu, Q., Dubouzet, J.G., Abe, H., Shinozaki, K., and Yamaguchi-Shinozaki, K. (2002). DNA-binding specificity of the ERF/AP2 domain of Arabidopsis DREBs, transcription factors involved in dehydration- and cold-inducible gene expression. Biochem. Biophys. Res. Commun. 290, 998-1009 https://doi.org/10.1006/bbrc.2001.6299
  30. Sakuma, Y., Maruyama, K., Osakabe, Y., Qin, F., Seki, M., Shinozaki, K., and Yamaguchi-Shinozaki, K. (2006a). Functional analysis of an Arabidopsis transcription factor, DREB2A, involved in drought-responsive gene expression. Plant Cell 18, 1292-1309 https://doi.org/10.1105/tpc.105.035881
  31. Sakuma, Y., Maruyama, K., Qin, F., Osakabe, Y., Shinozaki, K., and Yamaguchi-Shinozaki, K. (2006b). Dual function of an Arabidopsis transcription factor DREB2A in water-stress-responsive and heat-stress-responsive gene expression. Proc. Natl. Acad. Sci. USA 103, 18822-18827 https://doi.org/10.1073/pnas.0605639103
  32. Sambrook, J., and Russell, D.W. (2001). Molecular Cloning: A Laboratory Manual, 3rd eds., (New York, USA: Cold Spring Harbor Laboratory, Cold Spring Harbor)
  33. Song, C.P., Agarwal, M., Ohta, M., Guo, Y., Halfter, U., Wang, P., and Zhu, J.K. (2005). Role of an Arabidopsis AP2/EREBP-type transcriptional repressor in abscisic acid and drought stress responses. Plant Cell 17, 2384-2396 https://doi.org/10.1105/tpc.105.033043
  34. Uno, Y., Furihata, T., Abe, H., Yoshida, R., Shinozaki, K., and Yamaguchi-Shinozaki, K. (2000). Arabidopsis basic leucine zipper transcription factors involved in an abscisic acid-dependent signal transduction pathway under drought and high-salinity. Proc. Natl. Acad. Sci. USA 97, 11632-11637 https://doi.org/10.1073/pnas.190309197
  35. Xiong, L., Schumaker, K.S., and Zhu, J.-K. (2002). Cell signaling during cold, drought, and salt stress. Plant Cell 14, S165-S183 https://doi.org/10.1105/tpc.010278
  36. Yamaguchi-Shinozaki, K., and Shinozaki, K. (2005). Organization of cis-acting regulatory elements in osmotic- and cold-stressresponsive promoters. Trends Plant Sci. 10, 88-94 https://doi.org/10.1016/j.tplants.2004.12.012

피인용 문헌

  1. Isolation and functional characterization of CE1 binding proteins vol.10, pp.None, 2009, https://doi.org/10.1186/1471-2229-10-277
  2. AtNEK6 Interacts with ARIA and Is Involved in ABA Response during Seed Germination vol.29, pp.6, 2009, https://doi.org/10.1007/s10059-010-0070-7
  3. Abscisic Acid: Emergence of a Core Signaling Network vol.61, pp.None, 2009, https://doi.org/10.1146/annurev-arplant-042809-112122
  4. Arabidopsis Seed Germination Under Abiotic Stress as a Concert of Action of Phytohormones vol.15, pp.11, 2011, https://doi.org/10.1089/omi.2011.0082
  5. ABA-mediated transcriptional regulation in response to osmotic stress in plants vol.124, pp.4, 2009, https://doi.org/10.1007/s10265-011-0412-3
  6. Transfer of a Redox-Signal through the Cytosol by Redox-Dependent Microcompartmentation of Glycolytic Enzymes at Mitochondria and Actin Cytoskeleton vol.3, pp.None, 2012, https://doi.org/10.3389/fpls.2012.00284
  7. A novel abi5 allele reveals the importance of the conserved Ala in the C3 domain for regulation of downstream genes and salt tolerance during germination in Arabidopsis vol.8, pp.3, 2013, https://doi.org/10.4161/psb.23455
  8. Composition, Roles, and Regulation of Cullin-Based Ubiquitin E3 Ligases vol.12, pp.None, 2009, https://doi.org/10.1199/tab.0175
  9. De Novo Transcriptome Sequence Assembly and Identification of AP2/ERF Transcription Factor Related to Abiotic Stress in Parsley ( Petroselinum crispum ) vol.9, pp.9, 2014, https://doi.org/10.1371/journal.pone.0108977
  10. Arabidopsis Putative MAP Kinase Kinase Kinases Raf10 and Raf11 are Positive Regulators of Seed Dormancy and ABA Response vol.56, pp.1, 2015, https://doi.org/10.1093/pcp/pcu148
  11. Genome-Wide Analysis of the AP2/ERF Family in Eucalyptus grandis : An Intriguing Over-Representation of Stress-Responsive DREB1/CBF Genes vol.10, pp.4, 2009, https://doi.org/10.1371/journal.pone.0121041
  12. Arabidopsis MAP3K16 and Other Salt-Inducible MAP3Ks Regulate ABA Response Redundantly vol.40, pp.3, 2009, https://doi.org/10.14348/molcells.2017.0002
  13. Transcriptome profiling revealed novel transcriptional regulators in maize responses to Ostrinia furnacalis and jasmonic acid vol.12, pp.5, 2009, https://doi.org/10.1371/journal.pone.0177739
  14. Improvement of Drought Tolerance in Rice ( Oryza sativa L.): Genetics, Genomic Tools, and the WRKY Gene Family vol.2018, pp.None, 2009, https://doi.org/10.1155/2018/3158474
  15. A Phylogenetic Study of the ANT Family Points to a preANT Gene as the Ancestor of Basal and euANT Transcription Factors in Land Plants vol.10, pp.None, 2009, https://doi.org/10.3389/fpls.2019.00017
  16. OsMAPKKK63 is involved in salt stress response and seed dormancy control vol.14, pp.3, 2009, https://doi.org/10.1080/15592324.2019.1578633
  17. Transcriptome-based identification of AP2/ERF family genes and their cold-regulated expression during the dormancy phase transition of Chinese cherry flower buds vol.275, pp.None, 2009, https://doi.org/10.1016/j.scienta.2020.109666
  18. ABAP1 Plays a Role in the Differentiation of Male and Female Gametes in Arabidopsis thaliana vol.12, pp.None, 2009, https://doi.org/10.3389/fpls.2021.642758
  19. Integrated Transcriptomic and Bioinformatics Analyses Reveal the Molecular Mechanisms for the Differences in Seed Oil and Starch Content Between Glycine max and Cicer arietinum vol.12, pp.None, 2009, https://doi.org/10.3389/fpls.2021.743680
  20. TaAP2-15, An AP2/ERF Transcription Factor, Is Positively Involved in Wheat Resistance to Puccinia striiformis f. sp. tritici vol.22, pp.4, 2009, https://doi.org/10.3390/ijms22042080