Genome-wide association study revealed genetic variations of ABA sensitivity controlled by multiple stress-related genes in rice
Lei Peng, Tingting Xie, Zilong Guo, Xiaokai Li, Yu Chang, Haifu Tu, Shengchang Wang, Nai Wu, Yilong Yao, Lizhong Xiong
Genome-wide association study revealed genetic variations of ABA sensitivity controlled by multiple stress-related genes in rice
Abscisic acid (ABA) is a critical phytohormone that regulates multiple physiological processes including plant growth and stress tolerance. The core ABA signaling pathway has been well established, but genetic variations mediating ABA responses remain largely unknown. In this study, we performed genome-wide association study (GWAS) to identify loci and genes associated with ABA sensitivity (reflected by seed germination inhibition by ABA) in a panel of 425 rice accessions. The seed germination assay revealed that Aus and indica rice had stronger ABA sensitivity than japonica rice. A total of 48 non-redundant association loci were detected in the indica subpopulation and whole population, and 386 genes in these loci were responsive to ABA or abiotic stresses. Eight association loci were overlapped with previously reported loci for yield under drought stress or for drought-indicative image traits. Haplotype analyses of important candidate genes such as OsSAPK6, a key component in the ABA signaling core, were performed to identify key SNPs/InDels that may affect gene functions through promoter activity regulation, amino acid variation, or gene splicing. These results provide insights into the genetic basis of ABA sensitivity related to stress responses.
ABA sensitivity / Seed germination / Stress response / Rice
[1] |
|
[2] |
Batistič O, Rehers M, Akerman A, Schlücking K, Steinhorst L, Yalovsky S, Kudla J (2012) S-acylation-dependent association of the calcium sensor CBL2 with the vacuolar membrane is essential for proper abscisic acid responses. Cell Res 22(7):1155–1168. https://doi.org/10.1038/cr.2012.71
|
[3] |
|
[4] |
|
[5] |
|
[6] |
|
[7] |
|
[8] |
|
[9] |
|
[10] |
|
[11] |
|
[12] |
|
[13] |
García-León M, Cuyas L, El-Moneim DA, Rodriguez L, Belda-Palazón B, Sanchez-Quant E, Fernández Y, Roux B, Zamarreño ÁM, García-Mina JM, Nussaume L, Rodriguez PL, Paz-Ares J, Leonhardt N, Rubio V (2019) Arabidopsis ALIX regulates stomatal aperture and turnover of abscisic acid receptors. Plant Cell 31(10):2411–2429. https://doi.org/10.1105/tpc.19.00399
|
[14] |
|
[15] |
|
[16] |
|
[17] |
|
[18] |
|
[19] |
|
[20] |
|
[21] |
|
[22] |
|
[23] |
|
[24] |
|
[25] |
|
[26] |
|
[27] |
|
[28] |
|
[29] |
|
[30] |
|
[31] |
|
[32] |
|
[33] |
|
[34] |
|
[35] |
|
[36] |
|
[37] |
|
[38] |
|
[39] |
|
[40] |
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, Sham PC (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81(3):559–575. https://doi.org/10.1086/519795
|
[41] |
|
[42] |
|
[43] |
|
[44] |
|
[45] |
Soma F, Takahashi F, Yamaguchi-Shinozaki K, Shinozaki K (2021) Cellular Phosphorylation Signaling and Gene Expression in Drought Stress Responses: ABA-Dependent and ABA-Independent Regulatory Systems. Plants 10(4). https://doi.org/10.3390/plants10040756
|
[46] |
|
[47] |
|
[48] |
Tischer SV, Wunschel C, Papacek M, Kleigrewe K, Hofmann T, Christmann A, Grill E (2017) Combinatorial interaction network of abscisic acid receptors and coreceptors from Arabidopsis thaliana. Proc Natl Acad Sci U S A 114(38):10280–10285. https://doi.org/10.1073/pnas.1706593114
|
[49] |
|
[50] |
|
[51] |
|
[52] |
|
[53] |
|
[54] |
|
[55] |
Yu X, Niu X, Yang S, Li Y, Liu L, Tang W, Liu Y (2011) Research on heat and drought tolerance in rice(Oryza sativa L.) by overexpressing transcription factor OsbZIP60. Scientia Agricultura Sinica 44(20):4142–4149. https://doi.org/10.3864/j.issn.0578-1752.2011.20.002
|
[56] |
|
[57] |
|
[58] |
|
[59] |
|
[60] |
|
[61] |
|
[62] |
|
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