OsIAA6, a member of the rice Aux/IAA gene family, is involved in drought tolerance and tiller outgrowth

Plant Science

Volumn 236, Issue , 2015, Pages 304-312

  Jung, Harin ^a   Lee, Dong Keun ^a   Choi, Yang Do ^a,b   Kim, Ju Kon ^a  

^a Seoul National University   (South Korea)

^b Seoul National University   (South Korea)

Author keywords

Auxin signaling; Drought tolerance; OsIAA6; Rice; Tiller bud outgrowth

Indexed keywords

ORYZA SATIVA;

INDOLEACETIC ACID DERIVATIVE; PLANT PROTEIN;

ACCLIMATIZATION; DROUGHT; GENE EXPRESSION REGULATION; GENETICS; GROWTH, DEVELOPMENT AND AGING; METABOLISM; ORYZA; PHYSIOLOGY; PLANT STEM;

ACCLIMATIZATION; DROUGHTS; GENE EXPRESSION REGULATION; INDOLEACETIC ACIDS; ORYZA; PLANT PROTEINS; PLANT STEMS;

EID: 84929380116     PISSN: 01689452     EISSN: 18732259     Source Type: Journal    
DOI: 10.1016/j.plantsci.2015.04.018     Document Type: Article

References (70)

1. McSteen P. Auxin and monocot development. Cold Spring Harb. Perspect. Biol. 2010, 2:a001479.
2. Park C.-M. Auxin homeostasis in plant stress adaptation response. Plant Signal. Behav. 2007, 2:306-307.
3. Wang S., Bai Y., Shen C., Wu Y., Zhang S., Jiang D., Guilfoyle T.J., Chen M., Qi Y. Auxin-related gene families in abiotic stress response in Sorghum bicolor. Funct. Integr. Genomics 2010, 10:533-546.
4. Kazan K. Auxin and the integration of environmental signals into plant root development. Ann. Bot. 2013, 112:1655-1665.
5. Rahman A. Auxin: a regulator of cold stress response. Physiol. Plant. 2013, 147:28-35.
6. Abel S., Nguyen M.D., Theologis A. The PS-IAA4/5-like family of early auxin-inducible mRNAs in Arabidopsis thaliana. J. Mol. Biol. 1995, 251:533-549.
7. Kim J., Harter K., Theologis A. Protein-protein interactions among the Aux/IAA proteins. Proc. Natl. Acad. Sci. U. S. A. 1997, 94:11786-11791.
8. Ulmasov T., Murfett J., Hagen G., Guilfoyle T.J. Aux/IAA proteins repress expression of reporter genes containing natural and highly active synthetic auxin response elements. Plant Cell 1997, 9:1963-1971.
9. Kepinski S., Leyser O. The Arabidopsis F-box protein TIR1 is an auxin receptor. Nature 2005, 435:446-451.
10. Dharmasiri N., Dharmasiri S., Estelle M. The F-box protein TIR1 is an auxin receptor. Nature 2005, 435:441-445.
11. Kepinski S., Leyser O. Ubiquitination and auxin signaling a degrading story. Plant Cell 2002, 14:s81-s95.
12. TIR1-mediated poly-ubiquitination marks AUX/IAA proteins for degradation. Plant J. 2009, 59:100-109.
13. Ramos J.A., Zenser N., Leyser O., Callis J. Rapid degradation of auxin/indoleacetic acid proteins requires conserved amino acids of domain II and is proteasome dependent. Plant Cell 2001, 13:2349-2360.
14. Ouellet F., Overvoorde P.J., Theologis A. IAA17/AXR3: biochemical insight into an auxin mutant phenotype. Plant Cell 2001, 13:829-841.
15. Reed J.S. Roles and activities of Aux/IAA proteins in Arabidopsis. Trends Plant Sci. 2001, 6:420-425.
16. Nakamura A., Umemura I., Gomi K., Hasegawa Y., Kitano H., Sazuka T., Matsuika M. Production and characterization of auxin-insensitive rice by overexpression of a mutagenized rice IAA protein. Plant J. 2006, 46:297-306.
17. Song Y., You J., Xiong L. Characterization of OsIAA1 gene, a member of rice Aux/IAA family involved in auxin and brassinosteroid hormone responses and plant morphogenesis. Plant Mol. Biol. 2009, 70:297-309.
18. Overvoorde P., Fukaki H., Beeckman T. Auxin control of root development. Cold Spring Harb. Perspect. Biol. 2010, 2:a001537.
19. Jun N., Gaohang W., Zhenxing Z., Huanhuan Z., Yunrong W., Ping W. OsIAA23-mediated auxin signaling defines postembryonic maintenance of QC in rice. Plant J. 2011, 68:433-442.
20. Kitomi Y., Inahashi H., Takehisa H., Sato Y., Inukai Y. OsIAA13-mediated auxin signaling is involved in lateral root initiation in rice. Plant Sci. 2012, 190:116-122.
21. Zhu Z.-X., Liu T., Liu S.-J., Mao C.-Z., Wu Y.-R., Wu P. A gain-of-function mutation in OsIAA11 affects lateral root development in rice. Mol. Plant 2012, 5:154-161.
22. McSteen P., Leyser O. Shoot branching. Annu. Rev. Plant Biol. 2005, 56:353-374.
23. Doust A.N. Grass architecture: genetic and environmental control of branching. Curr. Opin. Plant Biol. 2007, 10:21-25.
24. Thimann K.V., Skoog F. Studies on the growth hormone of plants: III. The inhibiting action of the growth substance on bud development. Proc. Natl. Acad. Sci. U. S. A. 1933, 19:714-716.
25. Leyser O. Regulation of shoot branching by auxin. Trends Plant Sci. 2003, 8:541-545.
26. Aguilar-Martínez J.A., Poza-Carrión C., Cubas P. Arabidopsis BRANCHED1 acts as an integrator of branching signals within axillary buds. Plant Cell 2007, 19:458-472.
27. Arite T., Iwata H., Ohshima K., Maekawa M., Nakajima M., Kojima M., Sakakibara H., Kyozuka J. DWARF10, an RMS1/MAX4/DAD1 ortholog, controls lateral bud outgrowth in rice. Plant J. 2007, 51:1019-1029.
28. Booker J., Chatfield S., Leyser O. Auxin acts in xylem-associated or medullary cells to mediate apical dominance. Plant Cell 2003, 15:495-507.
29. Ferguson B.J., Beveridge C.A. Roles for auxin, cytokinin, and strigolactone in regulating shoot branching. Plant Physiol. 2009, 149:1929-1944.
30. Hayward A., Stirnberg P., Beveridge C., Leyser O. Interactions between auxin and strigolactone in shoot branching control. Plant Physiol. 2009, 151:400-412.
31. Minakuchi K., Kameoka H., Yasuno N., Umehara M., Luo L., Kobayashi K., Hanada A., Ueno K., Asami T., Yamaguchi S., Kyozuka J. FINE CULM1 (FC1) works downstream of strigolactones to inhibit the outgrowth of axillary buds in rice. Plant Cell Physiol. 2010, 51:1127-1135.
32. Dun E.A., de Saint Germain A., Rameau C., Beveridge C.A. Antagonistic action of strigolactone and cytokinin in bud outgrowth control. Plant Physiol. 2012, 158:487-498.
33. Takeda T., Suwa Y., Suzuki M., Kitano H., Ueguchi-Tanaka M., Ashikari M., Matsuoka M., Ueguchi C. The OsTB1 gene negatively regulates lateral branching in rice. Plant J. 2003, 33:513-520.
34. Kebrom T.H., Burson B.L., Finlayson S.A. Phytochrome B represses Teosinte Branched1 expression and induces sorghum axillary bud outgrowth in response to light signals. Plant Physiol. 2006, 140:1109-1117.
35. Cheong Y.H., Chang H.-S., Gupta R., Wang X., Zhu T., Luan S. Transcriptional profiling reveals novel interactions between wounding, pathogen, abiotic stress, and hormonal responses in Arabidopsis. Plant Physiol. 2002, 129:661-677.
36. Hannah M.A., Heyer A.G., Hincha D.K. A global survey of gene regulation during cold acclimation in Arabidopsis thaliana. PLoS Genet. 2005, 1:e26.
37. Wang C., Yang A., Yin H., Zhang J. Influence of water stress on endogenous hormone contents and cell damage of maize seedlings. J. Integr. Plant Biol. 2008, 50:427-434.
38. Jain M., Khurana J.P. Transcript profiling reveals diverse roles of auxin-responsive genes during reproductive development and abiotic stress in rice. FEBS J. 2009, 276:3148-3162.
39. Park H.C., Cha J.-Y., Yun D.-J. Roles of YUCCAs in auxin biosynthesis and drought stress responses in plants. Plant Signal. Behav. 2013, 8:e24495.
40. Liscum E., Reed J. Genetics of Aux/IAA and ARF action in plant growth and development. Plant Mol. Biol. 2002, 49:387-400.
41. Jain M., Kaur N., Garg R., Thakur J.K., Tyagi A.K., Khurana J.P. Structure and expression analysis of early auxin-responsive Aux/IAA gene family in rice (Oryza sativa). Funct. Integr. Genomics 2006, 6:47-59.
42. Matsui A., Ishida J., Morosawa T., Mochizuki Y., Kaminuma E., Endo T.A., Okamoto M., Nambara E., Nakajima M., Kawashima M., Satou M., Kim J.M., Kobayashi N., Toyoda T., Shinozaki K., Seki M. Arabidopsis transcriptome analysis under drought, cold, high-salinity and ABA treatment conditions using a tiling array. Plant Cell Physiol. 2008, 49:1135-1149.
43. Du H., Liu H., Xiong L. Endogenous auxin and jasmonic acid levels are differentially modulated by abiotic stresses in rice. Front. Plant Sci. 2013, 4:397.
44. Oh S.J., Kim Y.S., Kwon C.W., Park H.K., Jeong J.S., Kim J.-K. Overexpression of the transcription factor AP37 in rice improves grain yield under drought conditions. Plant Physiol. 2009, 150:1368-1379.
45. Song Y., Wang L., Xiong L. Comprehensive expression profiling analysis of OsIAA gene family in developmental processes and in response to phytohormone and stress treatments. Planta 2009, 229:577-591.
46. Park S.-H., Bang S.W., Jeong J.S., Jung H., Redillas M.C.F.R., Kim H.I., Kim Y.S., Kim J.-K. Analysis of the APXPGD1 and R1G1B constitutive gene promoters in various organs over three homozygous generations of transgenic rice plants. Planta 2012, 235:1397-1408.
47. Park S.-H., Jeong J.S., Redilas M.C.F.R., Jung H., Bang S.W., Kim Y.S., Kim J.-K. Characterization of the root-predominant gene promoter HPX1 in transgenic rice plants. Plant Biotechnol. Rep. 2013, 7:339-344.
48. Oh S.J., Song S.I., Kim Y.S., Jang H.-J., Kim S.Y., Kim M., Kim Y.K., Nahm B.H., Kim J.-K. Arabidopsis CBF3/DREB1A and ABF3 in transgenic rice increased tolerance to abiotic stress without stunting growth. Plant Physiol. 2005, 138:341-351.
49. Redillas M.C., Strasser R.J., Jeong J.S., Kim Y.S., Kim J.-K. The use of JIP test to evaluate drought-tolerance of transgenic rice overexpressing OsNAC10. Plant Biotechnol. Rep. 2011, 5:169-175.
50. Redillas M.C.F.R., Jeong J.S., Strasser R.J., Kim Y.S., Kim J.-K. JIP analysis on rice (Oryza sativa cv Nipponbare) grown under limited nitrogen conditions. J. Korean Soc. Appl. Biol. Chem. 2011, 54:827-832.
51. Dubin M.J., Bowler C., Benvenuto G. A modified Gateway cloning strategy for overexpressing tagged proteins in plants. Plant Methods 2008, 4:1-11.
52. Pater B.S., Mark F., Rueb S., Katagiri F., Chua N.H., Schilperoort R.A., Hensgens L.A. The promoter of the rice gene GOS2 is active in various different monocot tissues and binds rice nuclear factor ASF-1. Plant J. 1992, 2:837-844.
53. Zhang Y., Su J., Duan S., Ao Y., Dai J., Liu J., Wang P., Li Y., Li B., Feng D., Wang L., Wang H. A highly efficient rice green tissue protoplast system for transient gene expression and studying light/chloroplast-related processes. Plant Methods 2011, 7:30.
54. Jeong D.H., An S., Park S., Kang H.G., Park G.G., Kim S.R., Sim J., Kim Y.O., Kim M.K., Kim S.R., Kim J., Shin M., Jung M., An G. Generation of a flanking sequence-tag database for activation-tagging lines in japonica rice. Plant J. 2006, 45:123-132.
55. Theologis A., Huynh T.V., Davi R.W. Rapid induction of specific mRNAs by auxin in pea epicotyl tissue. J. Mol. Biol. 1985, 183:53-68.
56. Thakur J.K., Jain M., Tyagi A.K., Khurana J.P. Exogenous auxin enhances the degradation of a light down-regulated and nuclear-localized OsiIAA1, an Aux/IAA protein from rice, via proteasome. Biochim. Biophys. Acta 2005, 1730:196-205.
57. Redillas M.S., Jeong J.S., Kim Y.S., Jung H., Bang S.W., Choi Y.D., Ha S.H., Reuzeau C., Kim J.-K. The overexpression of OsNAC9 alters the root architecture of rice plants enhancing drought resistance and grain yield under field conditions. Plant Biotechnol. J. 2012, 10:792-805.
58. Park S.-H., Jeong J.S., Redillas M.C., Jung H., Bang S.W., Kim Y.S., Kim J.-K. Transgenic overexpression of UIP1, an interactor of the 3' untranslated region of the Rubisco small subunit mRNA, increases rice tolerance to drought. Plant Biotechnol. Rep. 2013, 7:83-90.
59. Jeong J.S., Kim Y.S., Redillas M.C., Jang G., Jung H., Bang S.W., Choi Y.D., Ha S.H., Reuzeau C., Kim J.K. OsNAC5 overexpression enlarges root diameter in rice plants leading to enhanced drought tolerance and increased grain yield in the field. Plant Biotechnol. J. 2013, 11:101-114.
60. Oh S.J., Kwon C.W., Choi D.W., Song S.I., Kim J.-K. Expression of barley HvCBF4 enhances tolerance to abiotic stress in transgenic rice. Plant Biotechnol. J. 2007, 5:646-656.
61. Wang Y., Li J. The plant architecture of rice (Oryza sativa). Plant Mol. Biol. 2005, 59:75-84.
62. Xu M., Zhu L., Shou H., Wu P. A PIN1 family gene, OsPIN1, involved in auxin-dependent adventitious root emergence and tillering in rice. Plant Cell Physiol. 2005, 46:1674-1681.
63. Lee M., Jung J.-H., Han D.-Y., Seo P.J., Park W.J., Park C.-M. Activation of a flavin monooxygenase gene YUCCA7 enhances drought resistance in Arabidopsis. Planta 2012, 235:923-938.
64. Kim I.L., Baek D., Park H.C., Chun H.J., Oh D.-H., Lee M.K., Cha J.Y., Kim W.Y., Kim M.C., Chung W.S., Bohnert H.J., Lee S.Y., Bressan R.A., Lee S.W., Yun D.J. Overexpression of Arabidopsis YUCCA6 in potato results in high-auxin developmental phenotypes and enhanced resistance to water deficit. Mol. Plant 2013, 6:337-349.
65. Woo Y.-M., Park H.-J., Su'udi M., Yang J.-I., Park J.-J., Back K., Park Y.M.G., An G. Constitutively wilted 1, a member of the rice YUCCA gene family, is required for maintaining water homeostasis and an appropriate root to shoot ratio. Plant Mol. Biol. 2007, 65:125-136.
66. Shi H., Chen L., Ye T., Liu X., Ding K., Chan Z. Modulation of auxin content in Arabidopsis confers improved drought stress resistance. Plant Physiol. Biochem. 2014, 82:209-217.
67. Nakashima K., Ito Y., Yamaguchi-Shinozaki K. Transcriptional regulatory networks in response to abiotic stresses in Arabidopsis and grasses. Plant Physiol. 2009, 149:88-95.
68. Shinozaki K., Yamaguchi-Shinozaki K. Gene networks involved in drought stress response and tolerance. J. Exp. Bot. 2007, 58:221-227.
69. Zhang S., Li G., Fang J., Chen W., Jiang H., Zou J., Liu X., Zhao X., Li X., Chu C., Xie Q., Jiang X., Zhu L. The interactions among DWARF10, auxin and cytokinin underlie lateral bud outgrowth in rice. J. Integr. Plant Biol. 2010, 52:626-638.
70. Xia K., Wang R., Ou X., Fang Z., Tian C., Duan J., Wang Y., Zhang M. OsTIR1 and OsAFB2 downregulation via OsmiR393 overexpression leads to more tillers, early flowering and less tolerance to salt and drought in rice. PLoS ONE 2012, 7. e30039.