Protein name | Gene ID | Length (aa) | Molecular weight (Da) | pI | Instability index | Stability | Aliphatic index | GRAVY index | pFam domain | Subcellular location | Remarks (Suggested biotechnological approach for inducing precocious flowering) |
---|---|---|---|---|---|---|---|---|---|---|---|
CsFT | Cs7g07420.1 | 207 | 23143.33 | 6.29 | 47.17 | Unstable | 70.14 | -0.928 | Rdx family | Extracellular | Ectopic expression of an FT homolog conferred an early flowering phenotype in trifoliate orange [75] |
CsCO | Cs5g20660.3 | 437 | 49268.88 | 6.87 | 34.13 | Stable | 87.92 | -0.216 | Methylenetetrahydrofolate reductase | Extracellular | CO overexpression resulted in early phenotype in Arabidopsis [76] |
CsSOC1 | Cs3g20780.1 | 1065 | 118360.4 | 5.23 | 45.83 | Unstable | 75.73 | -0.605 | KOW motif | Nuclear | Overexpression of SOC1 suppressed the late flowering phenotype in Arabidopsis [77] |
CsFLD | Cs7g24530.1 | 722 | 79152.14 | 9.35 | 34.26 | Stable | 88.86 | -0.191 | Flavin containing amine oxidoreductase | Nuclear | Overexpression of FLD induced early flowering in Brassica juncea [78] |
CsLFY | Cs7g19530.1 | 398 | 44568.31 | 7.64 | 37.11 | Stable | 75.58 | -0.569 | DNA Binding Domain (C-terminal) Leafy/Floricaula | Nuclear | Constitutively expression of LFY promoteed flower initiation in Arabidopsis [79] |
CsSVP | Cs1g20360.1 | 217 | 24646.96 | 6.18 | 56.63 | Unstable | 87.19 | -0.69 | SRF-type transcription factor (DNA-binding and dimerisation domain) | Nuclear | svp mutants passed more rapidly through the vegetative developmental stages in Arabidopsis [80] |
CsTFL | Cs6g15000.1 | 173 | 19388.09 | 7.96 | 48.61 | Unstable | 78.27 | -0.25 | Phosphatidylethanolamine-binding protein | Cytoplasmic | tfl1-1 mutation caused early flowering in Arabidopsis [81] |
CsBFT | Cs9g16990.1 | 173 | 19234.97 | 9.16 | 40.78 | Unstable | 78.84 | -0.305 | Phosphatidylethanolamine-binding protein | Cytoplasmic | BFT over-expression caused late flowering in Arabidopsis [82] |
CsMADS_AGL61 | Cs2g21850.4 | 433 | 49222.5 | 9.26 | 50.33 | Unstable | 72.29 | -0.897 | Zinc finger C-x8-C-x5-C-x3-H type | Extracellular | MADS_AGL genes regulate flowering via various regulatory pathways [83, 84] |
CsMADS_AGL82 | Cs6g13050.1 | 485 | 55194.13 | 9.16 | 38.26 | Stable | 92.14 | -0.247 | PPR repeat | Mitochondrial | |
CsMADS_AGL31 | Cs1g26410.2 | 519 | 59,579 | 4.55 | 52.02 | Unstable | 85.24 | -0.32 | Cyclin, N-terminal domain | Extracellular | |
CsMADS_AGL3 | Cs5g12270.1 | 175 | 20207.84 | 5.85 | 55.62 | Unstable | 85.77 | -0.592 | K-box region | Nuclear | |
CsMADS_AGL70 | Cs2g04260.3 | 447 | 51135.08 | 6.66 | 41.4 | Unstable | 94.88 | -0.327 | Protein tyrosine and serine/threonine kinase | Extracellular | |
CsMADS_AGL72 | Cs9g16575.1 | 85 | 9753.47 | 9.51 | 42.6 | Unstable | 75.65 | -0.146 | SRF-type transcription factor (DNA-binding and dimerisation domain) | Nuclear | |
CsMADS_AGL35 | Cs6g01880.1 | 237 | 27186.28 | 9.37 | 56.77 | Unstable | 67.47 | -0.713 | SRF-type transcription factor (DNA-binding and dimerisation domain) | Nuclear | |
CsTSF | Cs6g16420.1 | 146 | 16815.81 | 10.16 | 68.02 | Unstable | 76.1 | -0.638 | None | Membrane bound chloroplast | TSF overexpression caused a precocious flowering phenotype independent of photoperiods in Arabidopsis [85] |
CsAP3 | Cs1g24860.1 | 223 | 25761.15 | 9.39 | 44.23 | Unstable | 69.1 | -0.856 | SRF-type transcription factor (DNA-binding and dimerisation domain) | Nuclear | AP3 negatively regulates BANQUO genes whose expression promotes early flowering [86] |
CsAP2 | Cs8g17390.1 | 510 | 55237.62 | 6.06 | 51.41 | Unstable | 56.08 | -0.676 | AP2 domain | Nuclear | Over-expression of miRNA targeted AP2 and promotes early flowering [87] |
CsWUS | Cs8g17610.1 | 208 | 24103.7 | 9.33 | 68.12 | Unstable | 60.48 | -0.756 | Homeodomain | Nuclear | Overexpression of OsWOX13 (WUS Homeobox Transcription Factor) in rice resulted in early flowering [88] |
CsCRY1 | Cs3g18240.5 | 502 | 56830.21 | 5.33 | 55.05 | Unstable | 71.33 | -0.594 | FAD binding domain of DNA photolyase | Nuclear | Allele carrying the gain-of-function CRY2-Cvi flowers much earlier in Arabidopsis [89] |
CsCRY2 | Cs9g10510.2 | 644 | 73691.23 | 5.49 | 46.07 | Unstable | 77.55 | -0.487 | FAD binding domain of DNA photolyase | Nuclear | OsiCRY2 Arabidopsis over-expressers exhibited early flowering by 10–15 days in rice [90] |
CsDL4 | Cs4g01340.1 | 1633 | 183255.6 | 6.47 | 45.46 | Unstable | 93.04 | -0.163 | Ribonuclease III domain | Nuclear | Mutations of DL cause complete homeotic transformation of carpels into stamens [91] |
CsGI | Cs3g21790.7 | 941 | 103301.3 | 6.19 | 57.18 | Unstable | 93.72 | -0.05 | None | Nuclear | Overexpression of GI promoted early flowering in Arabidopsis [92] |
CsPHYB | Cs9g02220.2 | 1090 | 120896.4 | 5.84 | 44.14 | Unstable | 94.2 | -0.108 | Phytochrome region | Extracellular | Loss of function of GmPHYA2/E4 or GmPHYA3/E3 significantly shortened the time to flowering in soybean [93] |
CsFLK | Cs8g13220.1 | 521 | 56104.4 | 4.66 | 56.22 | Unstable | 70.33 | -0.565 | KH domain | Extracellular | Mutant having inactivated FLK via T-DNA insertion exhibited late flowering phenotype [94] |
CsSEP2 | Cs6g19680.1 | 243 | 27894.81 | 9.01 | 41.84 | Unstable | 83.09 | -0.674 | K-box region | Nuclear | Overexpression of SEP3 causes similar phenotypes as 35Â S:AP1 to promote the flowering of Arabidopsis [95] |
CsPI | Cs4g06140.3 | 238 | 27357.43 | 8.15 | 50.63 | Unstable | 92.14 | -0.445 | SRF-type transcription factor (DNA-binding and dimerisation domain) | Nuclear | Mutations in PI resulted in the homeotic transformation of petals to sepals and stamens to carpels [96] |
CsMAF1 | Cs2g14610.2 | 222 | 24322.14 | 9.65 | 46.95 | Unstable | 94.91 | 0.089 | Cofactor assembly of complex C subunit B | Extracellular | MAF2 overexpression between generations delays flowering in Arabidopsis [61] |
CsSHP1 | Cs7g16960.1 | 127 | 14425.72 | 10.01 | 57.53 | Unstable | 82.99 | -0.547 | SRF-type transcription factor (DNA-binding and dimerisation domain) | Nuclear | shp1 shp2 double mutant fruits do not open at maturity in Arabidopsis [97] |
CsCEN | Cs8g15080.1 | 172 | 19665.50 | 8.92 | 45.62 | Unstable | 76.40 | -0.357 | Phosphatidylethanolamine-binding protein | Cytoplasmic | Silencing GoCEN led to early flowering in cotton [98] |
CsFLC | Cs7g07200.1 | 200 | 22395.88 | 9.40 | 41.16 | Unstable | 98.60 | -0.308 | - | Nuclear | Loss-of-function of FLC promoted flowering in Arabidopsis [99] |
CsEMF1 | Cs4g24260.1 | 1247 | 137747.91 | 7.17 | 52.08 | Unstable | 61.57 | -0.755 | Protein EMBRYONIC FLOWER 1 | Extracellular | Loss-of-function mutations in Arabidopsis EMF produced a single terminal flower on all nodes [69] |
CsFRI | Cs7g14090.1 | 618 | 68196.92 | 8.63 | 48.26 | Unstable | 83.82 | -0.361 | Frigida-like | Nuclear | Early-flowering Arabidopsis ecotypes have loss of FRI function with alleles containing one of two different deletions that disrupt the open reading frame [66] |
CsTEM1 | Cs7g09120.1 | 377 | 41911.27 | 8.89 | 44.87 | Unstable | 67.48 | -0.640 | B3 domain-containing transcription factor LEC2-like | Extracellular | tem1-1 mutant enhanced the early flowering phenotype in Arabidospsis [100] |
CsSPB | Cs2g19530.1 | 189 | 21086.62 | 9.02 | 52.39 | Unstable | 49.58 | -1.110 | Squamosa promoter binding-like protein | Nuclear | Over-expression of SBP resulted in delayed flowering in Arabidopsis [101] |
CsSPL1 | Cs9g00360.2 | 1038 | 115346.83 | 8.31 | 53.05 | Unstable | 81.40 | -0.389 | Squamosa promoter binding-like protein | Nuclear | Ectopic expression of RcSPL1 in Arabidopsis accelerated the vegetative phase transition and flowering [102] |
CsSPL2 | Cs7g07070.8 | 480 | 52509.43 | 7.17 | 49.36 | Unstable | 58.35 | -0.678 | Squamosa promoter binding-like protein | Nuclear | Spl2 contribute to both juvenile-to-adult vegetative transition and the vegetative-to-reproductive transition in Arabidopsis [103] |
CsSUF4 | Cs2g13420.2 | 402 | 44137.22 | 7.66 | 63.33 | Unstable | 68.31 | -0.284 | - | Nuclear | suf4 mutant exhibited an earlier flowering phenotype in Arabidopsis [104] |
CsVIN3 | Cs7g01480.1 | 1211 | 134654.43 | 5.56 | 55.08 | Unstable | 61.11 | -0.828 | Protein OBERON | Nuclear | Vin3 mutants completely block vernalization response in Arabidopsis [72] |
CsVIP3 | Cs4g26180.2 | 315 | 34003.42 | 5.66 | 27.29 | Stable | 83.56 | -0.063 | - | Cytoplasmic | vip3 mutant plants flowered earlier than flc mutants in Arabidopsis [105] |
CsDELLA | Cs2g10860.1 | 594 | 65010.28 | 5.07 | 50.32 | Unstable | 78.10 | -0.252 | Transcription factor GRAS | Nuclear | Loss of individual DELLA genes resulted in only a minor hastening in flowering in Arabidopsis [106] |
CsZTL | Cs4g02700.1 | 616 | 67568.75 | 5.38 | 43.76 | Unstable | 83.78 | -0.168 | - | Cytoplasmic | Over expression of ZTL causes late flowering phenotype in Arabidopsis [107] |
CsFT3 | Cs7g24270.1 | 772 | 88200.25 | 9.13 | 42.98 | Unstable | 93.76 | -0.200 | QUIRKY-like | Extracellular | CcFT3 overexpression induced precocious flowering in many transgenic lines in Carrizo [108] |