Identification and Expression Analysis of GRAS Gene Family in Saccharum spontaneum
HUANG Cui-Lin1, LIN Ping-Ping2, ZHAO Xin-Wang2, ZHANG Mu-Qing1,*
1 Guangxi Key Laboratory of Sugarcane Biology/State Key Laboratory of Unitization and Conservation for Subtropical Agri-Biological Resources, Guangxi University, Nanning 530005, China; 2 National Sugarcane Engineering Technology Research Center, Fujian Agriculture and Forestry University, Fuzhou 350002, China
Abstract:Sugarcane (Saccharum officinarum) is an important sugar and biofuel crop, and its yield is affected by various biotic and abiotic stresses. S. spontaneum is one of the important parents in sugarcane cultivation and breeding. GRAS (GAI-RGA-SCR) transcription factors play important roles in the regulation of plant photomorphogenesis, seed germination, root growth and defense responses. In this study, 173 members of the GRAS gene family were identified from the genome of Saccharum spontaneum using the Hidden Markov Model (HMM) configuration file of the GRAS domain, which were distributed on 30 chromosomes of S. spontaneum. Phylogenetic analysis by maximum likelihood method showed that 173 GRAS genes of S. spontaneum could be further divided into 8 subfamilies. Motif and gene structure analysis showed that 173 GRAS genes contained at least one conserved GRAS domain at the C-terminal, and 61.2% of GRAS genes contained at least one intron. The analysis of cis-acting elements in the 2 000 bp sequence promoter upstream of 173 GRAS genes found that all GRAS promoter region had cis-acting elements in response to biotic and abiotic stresses, indicating that they might be involved in the regulation process of a variety of stress. The spatiotemporal transcriptional expression analysis found that the members of the GRAS family from S. spontaneum significantly expressed at different stages of stem and leaf development. qRT-PCR verified the expression of 9 genes in mature stem and leaf tissues, and the results were consistent with transcriptome data, suggesting that their family members played different roles in the growth and development regulation of S. spontaneum. The expression of SsPAT1.8-1 and SsDELLA6-2 were induced by the pathogen of sugarcane pokkah boeng disease; SsPAT1.8-2, SsPAT1.9, SsPAT1.10, SsDELLA2, SsSCR2, SsDELLA1-2, SsSCL3.1-2 and SsHAM9 were induced by Sugarcane mosaic virus (ScMV); SsSCL3.2-1 was induced by drought stress. qRT-PCR results showed that after ScMV infection, SsSCR2 was up-regulated in leaf +1 of resistant variety 'B48', SsHAM9 was up-regulated in leaf +1 and leaf -3, and SsLISCL11-1 was down-regulated in leaf -3. It is inferred that these GRAS family genes might play an important regulatory role in sugarcane response to different stresses. These results lay a foundation for further analyzing the function and regulation mechanism of GRAS family genes in sugarcane, and provide valuable gene resources for stress resistance breeding of sugarcane.
[1] 郭华军, 焦远年, 邸超, 等. 2009. 拟南芥转录因子 GRAS 家族基因群响应渗透和干旱胁迫的初步探索[J]. 植物学报, 44(3): 290-299. (Guo H J, Jiao Y N, Di C, et al. 2009. Preliminary exploration of Arabidopsis transcription factor GRAS family gene group in response to os-motic and drought stress[J]. Acta Botany Sinica, 44(3):290-299.) [2] 韩雯毓, 李国瑞, 风兰, 等. 2020. 蓖麻 GRAS 转录因子家族的全基因组分析及逆境胁迫响应[J]. 植物遗传资源学报, 21(01): 252-259. (Han W Y, Li G R, Feng L, et al. 2020. Genome wide analysis of castor GRAS transcription factor family and its response to stress[J]. Journal of Plant Genetic Resources, 21(01): 252-259.) [3] 李亚飞, 阳文龙, 顾晶晶, 等. 2019. 小麦 GRAS 基因家族的全基因组鉴定与分析[J]. 麦类作物学报, 39(5): 549-559. (Li Y F, Yang W L, Gu J J, et al. 2019. Whole ge-nome identification and analysis of GRAS gene family in wheat[J]. Journal of Wheat Crops, 39(5): 549-559.) [4] 刘云辉, 李珅, 王洋, 等. 2019. 药用植物中GRAS 转录因子的功能研究进展[J]. 浙江农林大学学报, 36(6): 1233-1240. (Liu Y H, Li S, Wang Y, et al. 2019. Research progress on the functions of GRAS transcription factors in medical plants[J]. Journal of Zhejiang A&F Universi-ty, 36(6): 1233-1240.) [5] 牛义岭.2017. 番茄 GRAS 基因家族生物信息学分析及部分抗性相关基因鉴定分析[D]. 硕士学位论文, 东北农业大学, 导师: 许向阳, pp. 28-38. (Niu Y L.2017. Bioin-formatics analysis of GRAS gene family and identification of some resistance related genes in tomato[D]. The-sis for M.S., Northeast Agricultural University, Supervi-sor: Xu X Y, pp. 28-38.) [6] 杨溥原, 梁红凯, 殷丛培, 等. 2021. 高粱 GRAS 基因家族全基因组鉴定及其对烯效唑的响应[J]. 河北农业大学学报, 44(05): 1-13. (Yang P Y, Liang H K, Yin C P, et al. 2021. Whole genome identification of sorghum GRAS gene family and its response to Uniconazole[J]. Journal of Hebei Agricultural University, 44(05): 1-13.) [7] Akbar S, Yao W, Yu K, et al. 2021. Photosynthetic character-ization and expression profiles of sugarcane infected by Sugarcane mosaic virus (SCMV)[J]. Photosynthesis Re-search, 150(1): 279-294. [8] Bolle C.2004. The role of GRAS proteins in plant signal transduction and development[J]. Planta, 218(5): 683-692. [9] Bolle C, Koncz C, Chua N H.2000. PAT1, a new member of the GRAS family, is involved in phytochrome A signal transduction[J]. Genes & Development, 14(10): 1269-1278. [10] Chen C, Chen H, Zhang Y, et al. 2020. TBtools: An integra-tive toolkit developed for interactive analyses of big bio-logical data[J]. Molecular Plant, 13(8): 1194-1202. [11] Day R B, Shibuya N, Minami E.2003. Identification and char-acterization of two new members of the GRAS gene family in rice responsive to N-acetylchitooligosaccha-ride elicitor[J]. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression, 1625(3): 261-268. [12] Derksen H, Rampitsch C, Daayf F.2013. Signaling cross-talk in plant disease resistance[J]. Plant Science, 207: 79-87. [13] D'Hont A, Grivet L, Feldmann P, et al. 1996. Characterisation of the double genome structure of modern sugarcane cultivars (Saccharum spp.) by molecular cytogenetics[J].Molecular and General Genetics, 250(4): 405-13. [14] Fan S, Zhang D, Gao C, et al. 2017. Identification, classification, and expression analysis of GRAS gene family in Malus domestica[J]. Frontiers in Physiology, 8: 253. [15] Finn R D, Coggill P, Eberhardt R Y, et al. 2016. The Pfam pro-tein families database: Towards a more sustainable fu-ture[J]. Nucleic Acids Research, 44(D1): D279-D285. Fode B, Siemsen T, Thurow C, et al. 2008. The Arabidopsis [16] GRAS protein SCL14 interacts with class Ⅱ TGA tran-scription factors and is essential for the activation of stress-inducible promoters[J]. The Plant Cell, 20(11):3122-3135. [17] Grivet L, Arruda P.2002. Sugarcane genomics: Depicting the complex genome of an important tropical crop[J]. Cur-rent Opinion in Plant Biology, 5(2): 122-127. [18] Guo A Y, Chen X, Gao G, et al. 2007. PlantTFDB: A compre-hensive plant transcription factor database[J]. Nucleic Acids Research, 36(suppl_1): D966-D969. [19] Guo Y, Wu H, Li X, et al. 2017. Identification and expression of GRAS family genes in maize (Zea mays L.)[J]. PLOS ONE, 12(9): e0185418. [20] Hirano K, Asano K, Tsuji H, et al. 2010. Characterization of the molecular mechanism underlying gibberellin perception complex formation in rice[J]. The Plant Cell, 22(8):2680-2696. [21] Hirsch S, Oldroyd G E.2009. GRAS-domain transcription factors that regulate plant development[J]. Plant Signal-ing & Behavior, 4(8): 698-700. [22] Hou X, Lee L Y C, Xia K, et al. 2010. DELLAs modulate jas-monate signaling via competitive binding to JAZs[J]. Developmental Cell, 19(6): 884-894. [23] Kamiya N, Itoh J I, Morikami A, et al. 2003. The SCARE-CROW gene's role in asymmetric cell divisions in rice plants[J]. The Plant Journal, 36(1): 45-54. [24] Katoh K, Standley D M.2013. MAFFT multiple sequence alignment software version 7: Improvements in perfor-mance and usability[J]. Molecular Biology and Evolution, 30(4): 772-780. [25] Kim J C, Lee S H, Cheong Y H, et al. 2001. A novel cold-in-ducible zinc finger protein from soybean, SCOF-1, en-hances cold tolerance in transgenic plants[J]. The Plant Journal, 25(3): 247-259. [26] Krzywinski M, Schein J, Birol I, et al. 2009. Circos: An infor-mation aesthetic for comparative genomics[J]. Genome Research, 19(9): 1639-1645. [27] Lam E, Shine J, Silva J D, et al. 2009. Improving sugarcane for biofuel: Engineering for an even better feedstock[J]. Global Change Biology Bioenergy, 1(3): 251-255. [28] Larkin M A, Blackshields G, Brown N P, et al. 2007. Clustal W and Clustal X version 2.0[J]. Bioinformatics, 23(21):2947-2948. [29] Lescot M, Déhais P, Thijs G, et al. 2002. PlantCARE, a data-base of plant cis-acting regulatory elements and a portal to tools for in silico analysis of promoter sequences[J]. Nucleic Acids Research, 30(1): 325-327. [30] Letunic I, Bork P.2021. Interactive tree of life (iTOL) v5: An online tool for phylogenetic tree display and annotation[J]. Nucleic Acids Research, 49(W1): W293-W296. [31] Lin H, Zhu W, Silva J C, et al. 2006. Intron gain and loss in segmentally duplicated genes in rice[J]. Genome Biolo-gy, 7(5): 1-11. [32] Lin Q, Wang D, Dong H, et al. 2012. Rice APC/C(TE) con-trols tillering by mediating the degradation of MONOC-ULM 1[J]. Nature Communications, 3(1): 1-8. [33] Ling H, Wu Q, Guo J, et al. 2014. Comprehensive selection of reference genes for gene expression normalization in sugarcane by real time quantitative RT-PCR[J]. PLOS ONE, 9(5): e97469. [34] Liu M, Huang L, Ma Z, et al. 2019. Genome-wide identification, expression analysis and functional study of the GRAS gene family in Tartary buckwheat (Fagopyrum ta- taricum)[J]. BMC Plant Biology, 19(1): 1-17. [35] Liu X, Widmer A.2014. Genome-wide comparative analysis of the GRAS gene family in Populus, Arabidopsis and rice[J]. Plant Molecular Biology Reporter, 32(6): 1129-1145. [36] Liu Y, Huang W, Xian Z, et al. 2017. Overexpression of Sl- GRAS40 in tomato enhances tolerance to abiotic stresses and influences auxin and gibberellin signaling[J]. Fron-tiers in Plant Science, 8: 1659. [37] Livak K J, Schmittgen T D.2001. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method[J]. Methods, 25(4): 402-408. [38] Mayrose M, Ekengren S K, Melech-Bonfil S, et al. 2006. A novel link between tomato GRAS genes, plant disease resistance and mechanical stress response[J]. Molecular Plant Pathology, 7(6): 593-604. [39] Morohashi K, Minami M, Takase H, et al. 2003. Isolation and characterization of a novel GRAS gene that regulates meiosis-associated gene expression[J]. Journal of Bio-logical Chemistry, 278(23): 20865-20873. [40] Ortiz-Ramírez C, Guillotin B, Xu X, et al. 2021. Ground tis-sue circuitry regulates organ complexity in maize and Setaria[J]. Science, 374(6572): 1247-1252. [41] Price M N, Dehal P S, Arkin A P.2010. FastTree 2 - approxi-mately maximum-likelihood trees for large alignments[J]. PLOS ONE, 5(3): e9490. [42] Pysh L D, Wysocka-Diller J W, Camilleri C, et al. 1999. The GRAS gene family in Arabidopsis: Sequence character-ization and basic expression analysis of the SCARE-CROW-LIKE genes[J]. The Plant Journal, 18(1): 111-119. [43] Redhead E, Bailey T L.2007. Discriminative motif discovery in DNA and protein sequences using the DEME algo-rithm[J]. BMC Bioinformatics, 8(1): 1-19. [44] Roy S W, Penny D.2007. Patterns of intron loss and gain in plants: Intron loss-dominated evolution and genome-wide comparison of O. sativa and A. thaliana[J]. Molecu-lar Biology and Evolution, 24(1): 171-181. [45] Stuurman J, Jäggi F, Kuhlemeier C.2002. Shoot meristem maintenance is controlled by a GRAS-gene mediated signal from differentiating cells[J]. Genes & Develop-ment, 16(17): 2213-2218. [46] Sun X, Jones W T, Rikkerink E H A.2012. GRAS proteins: The versatile roles of intrinsically disordered proteins in plant signalling[J]. Biochemical Journal, 442(1): 1-12. [47] Tian C, Wan P, Sun S, et al. 2004. Genome-wide analysis of the GRAS gene family in rice and Arabidopsis[J]. Plant Molecular Biology, 54(4): 519-532. [48] Wang L, Ding X, Gao Y, et al. 2020. Genome-wide identification and characterization of GRAS genes in soybean (Glycine max)[J]. BMC Plant Biology, 20(1): 1-21. [49] Wang Z, Wong D C J, Wang Y, et al. 2021. GRAS-domain transcription factor PAT1 regulates jasmonic acid bio-synthesis in grape cold stress response[J]. Plant Physiol-ogy, 186(3): 1660-1678. [50] Wheeler T J, Eddy S R.2013. nhmmer: DNA homology search with profile HMMs[J]. Bioinformatics, 29(19): 2487-2489. [51] Wu Z, Chen L, Yu Q, et al. 2019. Multiple transcriptional fac-tors control stomata development in rice[J]. New Phytol-ogist, 223(1): 220-232. [52] Xu K, Chen S, Li T, et al. 2015. OsGRAS23, a rice GRAS tran-scription factor gene, is involved in drought stress re-sponse through regulating expression of stress-respon-sive genes[J]. BMC Plant Biology, 15(1): 1-13. [53] Yao W, Ruan M, Qin L, et al. 2017. Field performance of transgenic sugarcane lines resistant to Sugarcane mosaic virus[J]. Frontiers in Plant Science, 8: 104. [54] Yoshida H, Hirano K, Sato T, et al. 2014. DELLA protein functions as a transcriptional activator through the DNA binding of the indeterminate domain family proteins[J]. Proceedings of the National Academy of Sciences of the USA, 111(21): 7861-7866. [55] Yuan Y, Yang X, Feng M, et al. 2021. Genome-wide analysis of R2R3-MYB transcription factors family in the auto-polyploid Saccharum spontaneum: An exploration of dominance expression and stress response[J]. BMC Ge-nomics, 22(1): 1-18. [56] Yu F, Wang P, Li X, et al. 2018. Characterization of chromo-some composition of sugarcane in nobilization by using genomic in situ hybridization[J]. Molecular Cytogenet-ics, 11(1): 1-8. [57] Zhang J, Zhang X, Tang H, et al. 2018. Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L[J]. Nature Genetics, 50(11): 1565-1573. [58] Zhang Z L, Ogawa M, Fleet C M, et al. 2011. Scarecrow-like 3 promotes gibberellin signaling by antagonizing master growth repressor DELLA in Arabidopsis[J]. Proceedings of the National Academy of Sciences of the USA, 108(5): 2160-2165. [59] Zhu J K.2002. Salt and drought stress signal transduction in plants[J]. Annual Review of Plant Biology, 53(1): 247-273.