This is an outdated version published on 30-01-2025. Read the
most recent version.
Research Articles
Early Access
Identification and characterization of genes that regulate flowering in pigeon pea (Cajanaus cajan): An in-silico exploration
Department of Botany, School of Applied Sciences, Centurion University of Technology and Management, Jatni, Bhubaneswar- 752 050, India; Centre of Excellence in Natural Products and Therapeutics, Department of Biotechnology and Bioinformatics, Sambalpur University, Jyoti Vihar, Burla, Sambalpur-768 019, Odisha, India
Department of Botany, School of Applied Sciences, Centurion University of Technology and Management, Jatni, Bhubaneswar- 752 050, India
Department of Botany, School of Applied Sciences, Centurion University of Technology and Management, Jatni, Bhubaneswar- 752 050, India
Department of Botany, School of Applied Sciences, Centurion University of Technology and Management, Jatni, Bhubaneswar- 752 050, India
Abstract
Pigeon pea is a versatile pulse crop extensively cultivated across Latin America, Asia and Africa. It serves as a rich source of protein and fibre. The life cycle of this annual crop is significantly influenced by the timing of flowering, which affects both seed production and the overall growth period. Variation in flowering time is influenced by both biotic and abiotic factors, making it a crucial adaptive trait in flowering plants. In this study, we aim to understand how the genetics of pigeon pea plants regulate their flowering time.
We employed 2 methods, HMM profile search and standalone BLAST search, to identify genes involved in flowering regulation in pigeon pea. Protein sequences of 6 known flowering regulators from Arabidopsis and related plants were retrieved from the NCBI database. The entire set of protein sequences from pigeon pea was used as the database for comparison. The top hits with more than 30 % identity and known conserved domains were considered true orthologs, resulting in the identification of 6 pigeon pea genes: CcFrigida, CcFrigida Like1, CcFrigida Like2, CcFrigida Es-sential1, CcTerminal Flowering1 and CcTerminal Flowering2. Through a thorough review, we identified floral repressive genes, such as FLC and its activators, as significant targets for promoting early flowering in plants.
Although considerable progress has been made in understanding the role of MADS-box genes in flower development, we still lack sufficient information about flowering genes and their specific impact on flowering traits in pigeon pea. This investigation will provide details about the biological basis of adaptive traits in this important pulse crop by examining flowering genes in pigeon pea.
References
- Mula MG, Saxena KB. Lifting the level of awareness on pigeon pea-a global perspective. Inter Crops Res Institute for the Semi-Arid Trop. 2010;pp. 540.
- Aja PM, Alum EU, Ezeani N, Nwali BU. Comparative phytochemical composition of Cajanaus cajan leaf and seed. Int J Microbiol Res. 2015;6 (1):pp.42–46.
- Moursi YS, Dawood MFA, Sallam A, Thabet SG, Alqudah AM. Antioxidant enzymes and their genetic mechanism in alleviating drought stress in plants. In: Organic solutes, oxidative stress and antioxidant enzymes under abiotic stressors; 2021. 22:pp.233–62. https://doi.org/10.1201/9781003022879-12
- Hecht V, Foucher F, Ferrándiz C, Macknight R, Navarro C, Morin J, et al. Conservation of Arabidopsis flowering genes in model legumes. Plant Physiol. 2005;137(4):pp. 1420–34. https://doi.org/10.1104/pp.104.057018
- Du L, Ma Z, Mao H. Duplicate genes contribute to variability in abiotic stress re-sistance in allopolyploid wheat. Plants. 2023;12(13):pp. 2465. https://doi.org/10.3390/plants12132465
- Durai AA, Premachandran MN, Govindaraj P, Malathi P, Viswanathan R. Variability in breeding pool of sugarcane (Saccharum spp.) for yield, quality and resistance to different biotic and abiot-ic stress factors. Sugar Tech. 2015;17:pp.107–15. https://doi.org/10.1007/s12355-014-0301-x
- Benedict C, Geisler MJB, Trygg J, Huner NPA. Consensus by democracy. Using meta-analyses of microarray and genomic data to model the cold acclimation signalling pathway in Arabidopsis. Plant Physiol. 2006;141(4):pp.1219–32. https://doi.org/10.1104/pp.106.083527
- Mir RR, Saxena RK, Saxena KB, Upadhyaya HD, Kilian A, Cook DR, et al. Whole-genome scanning for mapping deter-minacy in pigeon pea (Cajanus spp.). Plant Breed. 2012a;132:pp.472-78. https://doi.org/10.1111/j.1439-0523.2012.02009.x
- Liu B, Watanabe S, Uchiyama T, Kong F, Kanazawa A, Xia Z, et al. The soybean stem growth habit gene Dt1 is an ortholog of Arabidopsis terminal flower. Plant Physiol. 2010;153:pp.198–210. https://doi.org/10.1104/pp.109.150607
- He Y, Doyle MR, Amasino RM. PAF1-complex-mediated histone methylation of FLOWERING LOCUS C chromatin is required for the vernalization-responsive, winter-annual habit in Arabidopsis. Genes Dev. 2004;18(22):pp. 2774–84. https://doi.org/10.1101/gad.1244504
- Shen L, Zhang Y, Sawettalake N. A molecular switch for FLOWERING LOCUS C ac-tivation determines flowering time in Arabidopsis. Plant Cell. 2022;34(2):pp. 818-33. https://doi.org/10.1093/plcell/koab286
- Repinski SL, Kwak M, Gepts P. The common bean growth habit gene PvTFL1y is a functional homolog of Arabidopsis TFL1. Theor Appl Genet. 2012;124:pp.1539-47. https://doi.org/10.1007/s00122-012-1808-8
- Werner JD, Borevitz JO, Uhlenhaut NH, Ecker JR, Chory J, Weigel D . FRIGIDA-independent variation in flowering time of natural Arabidopsis thaliana accessions. Genet. 2005;170(3):pp.1197–207. https://doi.org/10.1534/genetics.104.036533
- Roux F, Touzet P, Cuguen J, Corre VL. How to be early flowering: an evolutionary per-spective. Trends Plant Sci. 2006;11(8):pp.375–81. https://doi.org/10.1016/j.tplants.2006.06.006
- Verslues PE, Bailey-Serres J, Brodersen C, Bukley TN, Conti L, Christmann A, et al. Burning questions for a warming and changing world: 15 unknowns in plant abiotic stress. Plant Cell. 2023;35(1):pp.67–108. https://doi.org/10.1093/plcell/koac263
- Tan YC, Kumar AU, Wong YP, Ling APK. Bioinformatics approaches and applications in plant biotechnology. Genet Eng Biotechnol. 2022;20(1):pp. 1–3. https://doi.org/10.1186/s43141-022-00394-5
- Chien PS, Chen PH, Lee CR, Chiou TJ. TWAS coupled with eQTL analysis reveals the ge-netic connection between gene expression and flowering time in Arabidopsis. BioRxiv. 2022;2022–12. https://doi.org/10.1101/2022.12.07.519424
- Wang X, Miao H, Lv C, Wu G. Genome-wide association study identifies a novel BMI1A QTL allele that confers FLC expression diversity in Arabidopsis thaliana. J Exp Bot. 2023;30:pp. 120. https://doi.org/10.1093/jxb/erad120
- Duan X, Zhang K, Duanmu H, Yu Y. The myosin family genes in soybean: Genome-wide identification and expression analysis. S Afr J Bot. 2023;160:pp. 338–46. https://doi.org/10.1016/j.sajb.2023.06.054
- Kaur H, Sidhu GS, Mittal A, Yadav IS, Mittal M, Singla D, et al. Comparative transcriptomics in alternate bearing cultivar Dashehari reveals the genetic model of flowering in mango. Front Genet. 2023;10(13):pp. 1061168. https://doi.org/10.3389/fgene.2022.1061168
- Mohanty JN, Nayak S, Jha S, Joshi RK. Transcriptome profiling of the floral buds and dis-covery of genes related to sex-differentiation in the dioecious cucurbit Coccinia grandis (L.) Voigt. Gene. 2017;626:pp. 395–406. https://doi.org/10.1016/j.gene.2017.05.058
- Kim S, Choi K, Park C, Hwang HJ, Lee I. SUPPRESSOR OF FRIGIDA4, encoding a C2H2-Type zinc finger protein, represses flowering by transcriptional activation of Arabidopsis FLOW-ERING LOCUS C. Plant Cell. 2006;18(11):pp. 2985-98. https://doi.org/10.1105/tpc.106.045179
- Choi K, Kim J, Hwang HJ, Kim S, Park C, Kim SY, Lee I. The FRIGIDA complex activates transcription of FLC, a strong flowering repressor in Arabidopsis, by recruiting chromatin modification factors. Plant Cell. 2011;23(1):pp. 289-303. https://doi.org/10.1105/tpc.110.075911
- Zhang Y, Zeng L. Crosstalk between ubiquitination and other post-translational pro-tein modifications in plant immunity. Plant Commun. 2020;1(4):pp. 1-18. https://doi.org/10.1016/j.xplc.2020.100041
- Lee J, Oh M, Park H, Lee I. SOC1 translocated to the nucleus by interaction with AGL24 directly regulates LEAFY. Plant J. 2008;(5):pp. 832-43. https://doi.org/10.1111/j.1365-313X.2008.03552.x
- Mohanty JN, Joshi RK. Molecular cloning, characterization and expression analysis of MADS-box genes associated with reproductive development in Momordica dioica Roxb. 3 Biotech. 2018;8(3):pp. 150. https://doi.org/10.1007/s13205-018-1176-4
- Zhang L, Jiménez-Gómez JM. Functional analysis of FRIGIDA using naturally occur-ring variation in Arabidopsis thaliana. Plant J. 2020;103(1):pp.154-65. https://doi.org/10.1111/tpj.14716
- Agarwal G, Garg V, Kudapa H, Doddamani D, Pazhamala LT, Khan AW, et al. Genome-wide dissection of AP2/ERF and HSP90 gene families in five legumes and expression profiles in chickpea and pigeon pea. Plant Biotechnol J. 2016;14(7):pp. 1563-77. https://doi.org/10.1111/pbi.12520
- Satheesh V, Jagannadham PTK, Chidambaranathan P, Jain PK, Srinivasan R. NAC transcription factor genes: genome-wide identification, phylogenetic, motif and cis-regulatory element analysis in pigeon pea (Cajanaus cajan (L.) Millsp.). Mol Biol Rep. 2014;41:pp. 7763-73. https://doi.org/10.1007/s11033-014-3669-5
- Mendapara I, Modha K, Patel S, Parekh V, Patel R, Chauhan D, et al. Characterization of CcTFL1 governing plant architecture in pigeon pea (Cajanaus cajan (L.) Millsp.). Plant. 2023;12(11):pp. 2168. https://doi.org/10.3390/plants12112168
- Wang H, Feng M, Jiang Y, Du D, Dong C, Zhang Z, et al. Thermosensitive SUMOylation of TaHsfA1 defines a dynamic ON/OFF molecular switch for the heat stress response in wheat. Plant Cell. 2023;pp. 192. https://doi.org/10.1093/plcell/koad192
- Roy D, Sadanandom A. SUMO mediated regulation of transcription factors as a mechanism for transducing environmental cues into cellular signaling in plants. Cell Mol Life Sci. 2021;78:pp. 2641-64. https://doi.org/10.1007/s00018-020-03723-4
- Lee HT, Park HY, Lee KC, Lee JH, Kim JK. Two Arabidopsis splicing factors, U2AF65a and U2AF65b, differentially control flowering time by modulating the expression or alterna-tive splicing of a subset of FLC upstream regulators. Plant. 2023;12(8):pp. 1655. https://doi.org/10.3390/plants12081655
- Chen C, Wanyu X, Gaopu Z, Han Z, Huimin L, Lin W, Tana W. Transcriptome sequencing analysis of flowering related genes in Prunus sibirica. Mol Plant Breed. 2022;8:pp. 13. https://doi.org/10.5376/mpb.2022.13.0027
- Li C, Zhang J, Zhang Q, Dong A, Wu Q, Zhu X, Zhu X. Genome-wide identification and analysis of the NAC transcription factor gene family in garden Asparagus (Asparagus officinalis). Genes. 2022;13(6):pp. 976. https://doi.org/10.3390/genes13060976
- Li C, Lin H, Dubcovsky J. Factorial combinations of protein interactions generate a multiplicity of florigen activation complexes in wheat and barley. Plant J. 2015;84(1):pp. 70-82. https://doi.org/10.1111/tpj.12960
- Lembinen S, Cieslak M, Zhang T, Mackenzie K, Elomaa P, Prusinkiewicz P, et al. Diversity of woodland strawberry inflores-cences arises from hetero-chrony regulated by TERMINAL FLOWER 1 and FLOWERING LOCUS T. Plant Cell. 2023;35(6):pp. 2079-94. https://doi.org/10.1093/plcell/koad086
- Mir RR, Kudapa H, Srikanth S, Saxena RK, Sharma A, Azam S, et al. Candidate gene analysis for determinacy in pi-geon pea (Cajanus spp.). Theor Appl Genet. 2014;127:pp. 2663-78. https://doi.org/10.1007/s00122-014-2406-8
- Mir RR, Kumar N, Jaiswal V, Girdharwal N, Prasad M, Balyan HS, Gupta PK. Genetic dissection of grain weight (GW) in bread wheat through QTL interval and association mapping. Mol Breed. 2012;29(4):pp. 963-72. https://doi.org/10.1007/s11032-011-9693-4
Downloads
Download data is not yet available.