Submitted Successfully!
To reward your contribution, here is a gift for you: A free trial for our video production service.
Thank you for your contribution! You can also upload a video entry or images related to this topic.
Version Summary Created by Modification Content Size Created at Operation
1 -- 2835 2022-07-20 12:15:58 |
2 format correct Meta information modification 2835 2022-07-21 04:03:48 |

Video Upload Options

Do you have a full video?

Confirm

Are you sure to Delete?
Cite
If you have any further questions, please contact Encyclopedia Editorial Office.
Mashilo, J.;  Shimelis, H.;  Maja, D.;  Ngwepe, R.M. Retrospective Genetic Analysis in Sweet Watermelon. Encyclopedia. Available online: https://encyclopedia.pub/entry/25334 (accessed on 13 April 2024).
Mashilo J,  Shimelis H,  Maja D,  Ngwepe RM. Retrospective Genetic Analysis in Sweet Watermelon. Encyclopedia. Available at: https://encyclopedia.pub/entry/25334. Accessed April 13, 2024.
Mashilo, Jacob, Hussein Shimelis, Dorcus Maja, Richard Mantlo Ngwepe. "Retrospective Genetic Analysis in Sweet Watermelon" Encyclopedia, https://encyclopedia.pub/entry/25334 (accessed April 13, 2024).
Mashilo, J.,  Shimelis, H.,  Maja, D., & Ngwepe, R.M. (2022, July 20). Retrospective Genetic Analysis in Sweet Watermelon. In Encyclopedia. https://encyclopedia.pub/entry/25334
Mashilo, Jacob, et al. "Retrospective Genetic Analysis in Sweet Watermelon." Encyclopedia. Web. 20 July, 2022.
Retrospective Genetic Analysis in Sweet Watermelon
Edit

Understanding the genetic basis of a crop’s qualitative and quantitative traits is vital to designing market preferred varieties. Sweet watermelon [Citrullus lanatus (Thunb.) Matsum. and Nakai var. lanatus; 2n = 2x = 22] is an important cucurbit crop belonging to the family Cucurbitaceae of the genus Citrullus. 

gene-editing technology transcriptome analysis quantitative trait loci retrospective genetic analysis sweet watermelon

1. Introduction

Sweet watermelon [Citrullus lanatus (Thunb.) Matsum. and Nakai var. lanatus; 2n = 2x = 22] is an important cucurbit crop belonging to the family Cucurbitaceae of the genus Citrullus [1]. Of the six species within the genus namely: C. lanatus var. citroides, C. mucosospermusC. colocynthisC. ecirrhosusC. rehmii, and C. naudinianus [1]. Sweet watermelon is the favourite and an extensively cultivated and consumed fruit crop. The fruit comprises of essential nutrients (i.e., N, P, K, Ca, Mg, Fe, Mn, Cu and Zn), and phytochemical compounds such as sugars (fructose, sucrose and glucose), amino acids (citrulline and arginine) and organic acids (citric and malic), and carotenoids (lycopene, phytoene, prolycopene, violaxanthin, neoxanthin, lutein and β-carotene) [2][3][4][5][6][7][8][9][10][11][12].
Consumer preferences for fruit and seed traits drive the purchasing and consumption patterns of watermelon in the marketplace. As a result, watermelon breeders are constantly faced with the task of developing ideal varieties that are desired by the market. Key aspects in the product profiles in a watermelon variety include desirable plant architecture, high leaf biomass and fruit yield, fruit quality (high sugar and lycopene contents), optimum fruit size, external fruit features such as rind stripe patterns and colour, fruit flesh colour, seedlessness, and acceptable seed coat colours. The targeted selection of qualitative and quantitative phenotypic traits can aid in breeding watermelon varieties that meet a range of requirements by consumers and growers.
Understanding the genetic control of economic phenotypic traits could inform the required selection criteria, genetic advancement, and use of complementary molecular breeding strategies. Essential qualitative and quantitative phenotypic traits in watermelon breeding are broadly grouped into plant, flower, fruit, and seed attributes. Plant traits include (leaf biomass and tenderness, plant height, number of primary and secondary branches per plant), flower traits (flowering rate and time, number of male and female flowers, a ratio of male to female flowers), fruit (length, width, weight and rind thickness) and seed (length, width, colour, and weight). Hence, knowledge of the genetic basis of the crop’s qualitative and quantitative phenotypic traits is vital to design market-preferred varieties.
Functional genes conditioning qualitative and quantitative phenotypic traits in watermelon have been identified through comparative genetic analysis [11][12][13][14][15][16][17]. Qualitative phenotypic traits in watermelon are conditioned by major genes [13][14][18][19][20][21][22]. On the contrary, multiple minor genes are involved in the regulation of quantitative phenotypic traits in watermelon [23][24][25][26][27][28][29][30]. Quantitative trait loci (QTL) analysis in watermelon identified several genomic regions linked to important traits for molecular breeding. The development of various molecular marker systems linked to qualitative and quantitative phenotypic traits allowed for genetic analysis and marker-assisted breeding in watermelon [24][29][31][32][33][34]. Genomic resources will further facilitate the breeding of novel watermelon cultivars. The QTL mapping of genes controlling the key traits will facilitate the application of gene-editing technology to accelerate the breeding process and allow for the timeous release of desirable watermelon varieties. The clustered, regularly interspaced, short palindromic repeats (CRISPR/Cas9) gene-editing technology has been integrated in a few breeding programs and led to the development of watermelon progenies with excellent qualitative and quantitative attributes [35][36][37][38]. The conventional breeding of consumer-and-industry preferred watermelon varieties will benefit from the application CRISPR/Cas9 gene-editing technology. This requires a detailed understanding of genetic and genomic resources and a genetic analysis of qualitative and quantitative phenotypic traits in watermelon. 

2. Genetic Regulation of Qualitative Phenotypic Traits in Sweet Watermelon

Watermelon genotypes show extensive variation in the qualitative phenotypic traits that can be selected for breeding market-preferred varieties. The following sections present the hitherto identified genes that govern variation in the qualitative traits of watermelon.

2.1. Leaf Attributes

2.1.1. Leaf Shape

Leaf shape in sweet watermelon is categorized into lobed and non-lobed leaf phenotypes [39][40][41]. The degree of leaf lobation varies from tri-lobate to penta-lobate, with wide and round lobes [39][40]. The lobes vary in size, which determines the overall leaf size and area. In Africa where watermelon leaves are consumed as a leafy vegetable, the shape and size of the leaf is an important trait for breeding consumer-desired varieties. The majority of cultivated watermelon varieties possess the lobed leaf phenotype, which is controlled by a single dominant gene, designated as ClLL1 [20]. Two genes, such as ORF18 and ORF22 (encoding a homeobox-leucine zipper-like protein), are thought to confer the lobed-leaf phenotype of watermelon [20]. There is need for molecular marker development of leaf phenotypes to facilitate the breeding of new varieties with desirable leaf attributes, including high leaf biomass production.

2.1.2. Leaf Bitterness

The tender cooked leaves of watermelon are widely consumed in sub-Saharan Africa (SSA). The leaves are sources of essential nutrients and phytochemical compounds [8][9][42]. The predominant phytochemical compound in the leaves is cucurbitacins, which results in bitterness [42]. Cucurbitacins possess various pharmacological and pharmaceutical values [43][44]. The following cucurbitacins, namely, B, D, E and E-glucoside, are reported to accumulate in the leaves of watermelon [42]. There are limited studies on the genetic analysis of bitterness in watermelon leaves. In the fruit, bitterness is reportedly conditioned by a single dominate gene [45][46]Cla007077Cla007078Cla007079 and Cla007080 genes regulate the biosynthesis of cucurbitacins B and E in watermelon fruit [47]. The gene ClBt (gene ID: Cla011508) regulate fruit-specific cucurbitacins biosynthesis in watermelon fruit [46]. Additionally, genes, namely, CcCDS1CcCDS2 and ClCDS1, regulate the cucurbitacins biosynthesis pathway via the catabolism of cucurbitadienol synthase [48]. Whether the genes causing fruit bitterness are the same as those in leaves has yet to be determined.

3. Flower Characteristics

3.1. Sex Expression

Sex expression is an important trait, which determines fruit set and yield development in watermelon. The following sex phenotypes are present in watermelon: monoecious (producing male and female flowers on the same plant), andromonoecious (male and hermaphrodite flowers on the same plant), partially andromonoecious (male, female, hermaphrodite and bisexual flowers on the same plant) and gynoecious (female flowers only on the same plant) [13][21]. Monoecious sex expression is a desirable trait for selfing and seed multiplication within the same genotype. Monoecious and andromonoecious sex expression are undesirable for hybrid breeding, because there is a need to emasculate male flowers for pollination and hybrid breeding [21]. Gynoecious sex phenotype does not require the removal of male flowers and is ideal for cultivar development. Dioecy (separate male and female plants) is a desirable sex phenotype for hybrid breeding, though not common in watermelon.
Genetic analysis between parents of gynoecious × monoecious flowers revealed the ratios of three monoecious: 1 gynoecious flower in the F2 populations, and 1 monoecious and 1 gynoecious ratios in the backcross population, indicating a that single gene controls monoecy in watermelon [13]. The ethylene biosynthesis gene CitACS4, which encodes for a flower-specific ACS enzyme, regulates monoecy in watermelon, favouring more male flowers than female flowers [49][50]. Natural mutations of the CitACS4 gene are responsible for converting female flowers into hermaphrodite flowers, monoecy into partial andromonoecy or andromonoecy in watermelon [51][52]. A recessive gene, pa (gene ID: ClCG01G020800), controls the occurrence of bisexual and hermaphrodite flowers in watermelon [52]. The following genes are reportedly involved in ethylene biosynthesis and signalling, flower development and sex determination in watermelon: ClCG01G020030, ClCG01G020040ClCG01G020060ClCG01G020080ClCG01G020260ClCG01G020430, ClCG01G020700ClCG01G020770ClCG01G020780ClCG01G020790 and ClCG01G020800 [52]. Starch and sucrose metabolism genes such as Cla021762Cla004462Cla015099Cla009288Cla011403Cla017383 and Cla005857, phenylpropanoid biosynthesis genes including Cla005785Cla020908Cla009234Cla015297Cla015296 and Cla012598, pentose and glucuronate interconversions genes, and nitrogen metabolism genes Cla017784Cla017687Cla010086Cla005080 and Cla002787 are involved in the development of male flowers in watermelon [53]. Of these, a pollen-specific gene, Cla001608, plays a key role in the development of male flowers. The multiple genes involved in flower development indicate the presence of a complex metabolic pathway in sex expression in watermelon.

3.2. Male Sterility

Watermelon hybrid cultivar development involves the recombination of desirable contrasting parental genotypes. The complex sex phenotypes, including monoecy, limit hybrid breeding due to laborious procedures in genotype emasculation, isolation and pollination. Male sterility provides an alternative approach to the rapid and efficient breeding of watermelon hybrid varieties. Quantitative genetic analysis between male sterile and fertile watermelon genotypes revealed a 3:1 segregation ratio in the F2 populations [22], indicating a single dominant gene confer male sterility in watermelon. Rhee et al. (54) identified 1259 differentially expressed genes associated with male sterility through comparative transcriptome analysis. These genes are involved in various physiological processes, including stamen and pollen development and pollen tube elongation [54]. Some of the reported genes included Cla021983Cla015362Cla006728Cla016924Cla022958Cla022957Cla022600Cla013638Cla015385 and Cla006729 [54]. Of the stated genes, Cla006625, which encodes a pollen-specific leucine-rich repeat protein (ClaPEX1), resulted in sterile male flowers [22]Cla009410Cla007521Cla006625, Cla006738Cla006737 and Cla009382, reportedly up-regulated male-sterillity in watermelon [22]. The gene Citrullus lanatus Abnormal Tapetum 1 (ClATM1), which encodes a basic helix-loop-helix (bHLH) transcription factor, regulates flower development in watermelon [55]. The disruption of ClATM1 results in male sterility in watermelon [55]. Recently, CER1FARLOX2SHPLOPRCHS and F3H, were identified as regulating male sterility in watermelon, being involved in anther cuticle and pollen wall development [56]. The identified male sterility genes will facilitate hybrid breeding and deliver the desired watermelon cultivars.

4. Genetic Regulation of Quantitative Traits in Sweet Watermelon

Morphological diversity analysis in sweet watermelon revealed extensive variation in quantitative phenotypic traits, including plant architecture, flowering time and rates, fruit and seed yield, and fruit- and seed-related traits [41][57][58][59]. The section below outlines the genetic analysis of various quantitative traits.

4.1. Leaf Biomass Yield and Its Components

High leaf biomass yield in watermelon is a desired trait for use as a leaf vegetable. High leaf biomass production is also vital to enhancing photosynthetic efficiency to promote high fruit production and yield. The number of leaves per plant, which is influenced by plant height and branching capacity, as well as the length, width and size of individual leaves, are important traits that influence the overall leaf biomass yield in watermelon. A genetic analysis of leaf traits has not been adequately studied in watermelon. There are no molecular markers or QTL mapping of leaf traits for efficient selection and marker-assisted breeding. Some accessions of white-fleshed citron watermelon (Citrullus lanatus var. citroides) exhibit a reduced leaf size compared to most commercially cultivated sweet watermelons. These germplasms may play a key role in understanding the genetic architecture of leaf yield and component traits in watermelon.

4.2. Plant Height

Plant height is an important trait that influences flower development and fruit yield potential in watermelon. The candidate gene Cla010726 is associated with reduced plant height in watermelon [60]. The expression levels of Cla010726 are significantly lower in short plants [60]. The genes designated as Cla015405 and Cla015406 are associated with a short phenotype in watermelon [61]. Recently, Cla015407, named Citrullus lanatus dwarfism (Cldf), has been thought to control short plant stature in watermelon [62]. A point mutation resulting in a 13 bp deletion in the coding sequence of Cldf led to a GA-deficient short phenotype [63]. The gene Cla010726 encodes for gibberellin 20-oxidase-like protein, whereas Cla015407 gene encodes gibberellic acid 3β-hydroxylase proteins, which are associated with the gibberellic acid metabolism, resulting in growth arrest and reduced plant height [62]. The gene designated as Cla010337, which encodes an ATP-binding cassette transporter (ABC transporter), reportedly conditioned dwarf plant height in watermelon [64]. The deletion of a single nucleotide of the gene Cla010337 causes the development of shorter watermelon plants [64]. Quantitative analysis revealed segregation ratios of 3:1 and 1:1 in the F2 and backcross populations, suggesting that reduced plant height is controlled by a single recessive or dominant gene [62][65][66]. Cho et al. [66] identified the gene CICG09G018320, which encodes an ABC transporter, determining shorter watermelon plants in progenies derived between dwarf (Bush Sugar Baby) and normal (PCL-J1) watermelon cultivars. The ABC transporter gene results in shorter watermelon plants due to physiological changes in the levels of auxin, the phytohormone [66]. Internode length is a secondary trait that influences plant height in watermelon. Segregation ratios of 3:1 and 1:1 in the F2 and backcross populations, respectively, were detected, suggesting that a single dominant gene controls the expression of short internode length in watermelon [29]. The gibberellin 3β-hydroxylase (GA 3β-hydroxylase) gene Cla015407 is associated with the short internode phenotype in watermelon [29]. GA 3β-hydroxylase is an important enzyme regulating GA biosynthesis by catalyzing the inactive precursors of GA9, GA20, and GA5 into bioactive forms, namely, GA4, GA1, and GA3, respectively [29].

4.3. Branching Capacity

Branching capacity is an important trait influencing leaf biomass production, flowering potential, vine and fruit yield in watermelon. In SSA, the dried branches of the crop are used as fodder for livestock. The branches are a good source of essential macro- and micro-nutrients [8]. Watermelon produces multiple lateral branches from the primary branches. A single recessive gene, Clbl (i.e., Citrullus lanatus branchless), causes branchlessness [67]. Bulked segregant sequencing (BSA-seq) analysis revealed a candidate gene, Cla018392, which encodes a TERMINAL FLOWER 1 protein associated with branchlessness in watermelon [67]. This gene reduces the formation and development of axillary and apical buds, thus limiting lateral branching in watermelon [67]. Genetic analysis of lateral branch development in watermelon is key for marker-assisted selection and QTL mapping. This enables the breeding of branchless watermelon cultivars for closed and protected production or open field environments. However, the branchless trait is not required in watermelon grown for high leaf biomass for food feed. Therefore, understanding the genetic regulation of profuse branching ability is essential for breeding of vegetable- and fodder-type watermelon varieties. Researchers propose a comparative genetic analysis of watermelon genotypes with contrasting branching capacities to obtain insight into and elucidate the molecular mechanisms regulating this trait for breeding.

4.4. Flowering Time

Flowering time is another important trait influencing yield expression and potential in watermelon. Male and female flowers in watermelon are located separately on different nodes of the same plant. Male flowers appear first, followed by female flowers. The number of days before the appearance of the first male and female flowers extensively vary in watermelon. For example, McGregor and Waters [68] reported that the days to first male flower varied from 8 to 22 days after transplanting (DAT), and between 20 and 30 DAT to the first female flower among watermelon pollen parents. Stone et al. [69] reported days to first male flower varied between 44 and 60 days after planting (DAP), whereas days to first female flower varied between 52 and 70 DAP. Gimode et al. [32] reported that days to first female flower ranged from 16 to 37 DAP in watermelon. Flowering time in watermelon is subject to genotype, environment and genotype-by-environment interactions. The following genes: Cla009504 and Cla000855 [24] and Cla002795 (i.e., phosphatidylinositol-4-phosphate 5-kinase (PIP-kinase) [32] regulate flowering time in watermelon. The identified genes provide opportunities for breeding watermelon varieties with desired flowering times for different production environments, and in the development of molecular markers to ensure efficient selection for earliness.

4.5. Fruit Yield and Its Components

Fruit yield is an economic trait in watermelon, and varies considerably among the diverse varieties. Fruit yield ranging from 40.5 to 84 tons/ha has been reported in watermelon [70]. Stone et al. [69] reported fruit yield varying from 2.8 to 5.7 tons per hectare. Fruit yield in watermelon is determined by fruit weight, length and width. Fruit weight vary considerably in watermelon. Stone et al. [69] reported a single fruit weight of watermelon varying from ~ 3 to 12 kg, whereas Singh et al. [71] reported fruit weight varying from 0.10 to 3.21 kg. A fruit weight ranging from 0.58 to 8.2 kg has been reported in a diverse panel of watermelon varieties [41]. Fruit length and width also vary considerably between 21 and 40 cm, and from 20 to 25 cm, respectively [69], and from 10.9 to 20.9 cm and 9.20 to 34.6 cm [41]. Other secondary traits including plant height, the number of primary, secondary and tertiary branches, the number of male and female flowers, and the number of fruits produced per plant from successfully fertilized female flowers indirectly contribute to fruit yield in watermelon. As a result, fruit yield is influenced by several yield components [23][30][72]. Multiple QTLs associated with yield component traits have been reported in watermelon [23][24][28][30][72]. The multiple QTLs conditioning yield component traits are useful for the strategic breeding of watermelon for high fruit yield potential.

4.6. Seed Yield and Its Components

Triploid seedless watermelons are preferred for fresh consumption. Triploid watermelons produce non-viable pollen and require a diploid (seeded) watermelon as a pollen parent [73][74][75]. The production and breeding of seeded watermelons has declined in recent years in favour of seedless watermelons. Elsewhere, seeded watermelons are preferred for seed consumption as snack and for developing value-added by-products. In such circumstances, breeding watermelon varieties with a high seed yield is an important objective. Seed yield potential is determined by the number of seeds per fruit, seed, length, width, weight and size, which are highly variable in watermelon [76][77]. Small seed sizes are preferred for fresh fruit consumption, whereas large seeds are preferred for planting and cooking. Seed size in watermelon is categorized as tomato, small, medium, and large [78]. Two candidate genes, namely, Cla97C05G104360 and Cla97C05G104380, and three other genes, namely, Cla97C05G104340Cla97C05G104350 and Cla97C05G104390 [79], conditioned seed size through their involvement in abscisic acid metabolism. The genes Cla009290Cla009291 and Cla009310 were reportedly involved in seed size development [27]. Seed size is determined by seed length and width, which are conditioned by several QTLs [25][27][30]. Various QTLs are reported to control seed component traits in watermelon [25][27][30]. The mapped QTLs for seed component traits offer strategic breeding of watermelon varieties, targeting high seed yield potential.

References

  1. Chomicki, G.; Renner, S.S. Watermelon origin solved with molecular phylogenetics including Linnaean Material: Another example of Museomics. New Phytol. 2015, 205, 526–532.
  2. Lewinsohn, E.; Sitrit, Y.; Bar, E.; Azulay, Y.; Meir, A.; Zamir, D.; Tadmor, Y. Carotenoid pigmentation affects the volatile composition of tomato and watermelon fruits, as revealed by comparative genetic analyses. J. Agric. Food Chem. 2005, 53, 3142–3148.
  3. Tadmor, Y.; King, S.; Levi, A.; Davis, A.; Meir, A.; Wasserman, B.; Hirschberg, J.; Lewinsohn, E. Comparative fruit colouration in watermelon and tomato. Food Res. Int. 2005, 38, 837–841.
  4. Perkins-Veazie, P.; Collins, J.K.; Davis, A.R.; Roberts, W. Carotenoid Content of 50 Watermelon Cultivars. J. Agric. Food Chem. 2006, 54, 2593–2597.
  5. Liu, C.; Zhang, H.; Dai, Z.; Liu, X.; Liu, Y.; Deng, X.; Chen, F.; Xu, J. Volatile chemical and carotenoid profiles in watermelons with different flesh colors. Food Sci. Biotechnol. 2012, 21, 531–541.
  6. Yoo, K.S.; Bang, H.; Lee, E.J.; Crosby, K.M.; Patil, B. Variation of carotenoid, sugar, and ascorbic acid concentrations in watermelon genotypes and genetic analysis. Hortic. Environ. Biotechnol. 2012, 53, 552–560.
  7. Ren, Y.; McGregor, C.; Zhang, Y.; Gong, G.; Zhang, H.; Guo, S.; Sun, H.; Cai, W.; Zhang, J.; Xu, Y. An integrated genetic map based on four mapping populations and quantitative trait loci associated with economically important traits in watermelon (Citrullus lanatus). BMC Plant Biol. 2014, 14, 33.
  8. Huang, Y.; Zhao, L.; Kong, Q.; Cheng, F.; Niu, M.; Xie, J.; Nawaz, M.A.; Bie, Z. Comprehensive mineral nutrition analysis of watermelon grafted onto two different rootstocks. Hortic. Plant J. 2016, 2, 105–113.
  9. Tabiri, B.; Agbenorhevi, J.K.; Wireko-Manu, F.D.; Ompouma, E.I. Watermelon seeds as food: Nutrient composition, phytochemicals and antioxidant Activity. Int. J. Nutr. Food Sci. 2016, 5, 139.
  10. Gao, L.; Zhao, S.; Lu, X.; He, N.; Liu, W. ‘SW’, A new watermelon cultivar with a sweet and sour flavour. HortScience 2018, 53, 895–896.
  11. Jin, B.; Lee, J.; Kweon, S.; Cho, Y.; Choi, Y.; Lee, S.J.; Park, Y. Analysis of flesh color-related carotenoids and development of a CRTISO gene-based DNA marker for prolycopene accumulation in watermelon. Hortic. Environ. Biotechnol. 2019, 60, 399–410.
  12. Jawad, U.M.; Gao, L.; Gebremeskel, H.; Bin Safdar, L.; Yuan, P.; Zhao, S.; Xuqiang, L.; Nan, H.; Hongju, Z.; Liu, W. Expression pattern of sugars and organic acids regulatory genes during watermelon fruit development. Sci. Hortic. 2020, 265, 109102.
  13. Ji, G.; Zhang, J.; Gong, G.; Shi, J.; Zhang, H.; Ren, Y.; Guo, S.; Gao, J.; Shen, H.; Xu, Y. Inheritance of sex forms in watermelon (Citrullus lanatus). Sci. Hortic. 2015, 193, 367–373.
  14. Dou, J.; Lu, X.; Ali, A.; Zhao, S.; Zhang, L.; He, N.; Liu, W. Genetic mapping reveals a marker for yellow skin in watermelon (Citrullus lanatus L.). PLoS ONE 2018, 13, e0200617.
  15. Dou, J.; Zhao, S.; Lu, X.; He, N.; Zhang, L.; Ali, A.; Kuang, H.; Liu, W. Genetic mapping reveals a candidate gene (ClFS1) for fruit shape in watermelon (Citrullus lanatus L.). Theor. Appl. Genet. 2018, 131, 947–958.
  16. Legendre, R.; Kuzy, J.; McGregor, C. Markers for selection of three alleles of ClSUN25-26-27a (Cla011257) associated with fruit shape in watermelon. Mol. Breed. 2020, 40, 19.
  17. Liu, S.; Gao, Z.; Wang, X.; Luan, F.; Dai, Z.; Yang, Z.; Zhang, Q. Nucleotide variation in the phytoene synthase (ClPsy1) gene contributes to golden flesh in watermelon (Citrullus lanatus L.). Theor. Appl. Genet. 2021, 135, 185–200.
  18. Guner, N.; Wehner, T.C. The Genes of Watermelon. HortScience 2004, 39, 1175–1182.
  19. Gusmini, G.; Wehner, T.C. Genes Determining Rind Pattern Inheritance in Watermelon: A Review. HortScience 2005, 40, 1928–1930.
  20. Wei, C.; Chen, X.; Wang, Z.; Liu, Q.; Li, H.; Zhang, Y.; Ma, J.; Yang, J.; Zhang, X. Genetic mapping of the LOBED LEAF 1 (ClLL1) gene to a 127.6-kb region in watermelon (Citrullus lanatus L.). PLoS ONE 2017, 12, e0180741.
  21. Prothro, J.; Abdel-Haleem, H.; Bachlava, E.; White, V.; Knapp, S.; McGregor, C. Quantitative trait loci associated with sex expression in an inter-subspecific watermelon population. J. Am. Soc. Hortic. Sci. 2013, 138, 125–130.
  22. Dong, W.; Wu, D.; Yan, C.; Wu, D. Mapping and analysis of a novel genic male sterility gene in watermelon (Citrullus lanatus). Front. Plant Sci. 2021, 12, 611.
  23. Sandlin, K.; Prothro, J.; Heesacker, A.; Khalilian, N.; Okashah, R.; Xiang, W.; Bachlava, E.; Caldwell, D.G.; Taylor, C.A.; Seymour, D.K.; et al. Comparative mapping in watermelon (Citrullus lanatus (Thunb.) Matsum. et Nakai). Theor. Appl. Genet. 2012, 125, 1603–1618.
  24. McGregor, C.; Waters, V.; Vashisth, T.; Abdel-Haleem, H. Flowering time in watermelon is associated with a major quantitative trait locus on chromosome 3. J. Am. Soc. Hortic. Sci. 2014, 139, 48–53.
  25. Kim, K.-H.; Hwang, J.-H.; Han, D.-Y.; Park, M.; Kim, S.; Choi, D.; Kim, Y.; Lee, G.P.; Kim, S.T.; Park, Y.-H. Major quantitative trait loci and putative candidate genes for powdery mildew resistance and fruit-related traits revealed by an intraspecific genetic map for watermelon (Citrullus lanatus var. lanatus). PLoS ONE 2015, 10, e0145665.
  26. Li, B.; Lu, X.; Dou, J.; Aslam, A.; Gao, L.; Zhao, S.; He, N.; Liu, W. Construction of a high-density genetic map and mapping of fruit traits in watermelon (Citrullus lanatus L.) based on whole-genome resequencing. Int. J. Mol. Sci. 2018, 19, 3268.
  27. Li, N.; Shang, J.; Wang, J.; Zhou, D.; Li, N.; Ma, S. Fine mapping and discovery of candidate genes for seed size in watermelon by genome survey sequencing. Sci. Rep. 2018, 8, 17843.
  28. Fall, L.A.; Perkins-Veazie, P.; Ma, G.; McGregor, C. QTLs associated with flesh quality traits in an elite × elite watermelon population. Euphytica 2019, 215, 30.
  29. Gebremeskel, H.; Dou, J.; Li, B.; Zhao, S.; Muhammad, U.; Lu, X.; He, N.; Liu, W. Molecular mapping and candidate gene analysis for GA3 responsive short internode in watermelon (Citrullus lanatus). Int. J. Mol. Sci. 2019, 21, 290.
  30. Liang, X.; Gao, M.; Amanullah, S.; Guo, Y.; Liu, X.; Xu, H.; Liu, J.; Gao, Y.; Yuan, C.; Luan, F. Identification of QTLs linked with watermelon fruit and seed traits using GBS-based high-resolution genetic mapping. Sci. Hortic. 2022, 303, 111237.
  31. Liu, S.; Gao, P.; Wang, X.; Davis, A.R.; Baloch, A.M.; Luan, F. Mapping of quantitative trait loci for lycopene content and fruit traits in Citrullus lanatus. Euphytica 2014, 202, 411–426.
  32. Gimode, W.; Clevenger, J.; McGregor, C. Fine-mapping of a major quantitative trait locus Qdff3-1 controlling flowering time in watermelon. Mol. Breed. 2019, 40, 3.
  33. Yang, T.; Amanullah, S.; Pan, J.; Chen, G.; Liu, S.; Ma, S.; Wang, J.; Gao, P.; Wang, X. Identification of putative genetic regions for watermelon rind hardness and related traits by BSA-seq and QTL mapping. Euphytica 2021, 217, 1–18.
  34. Wang, D.; Zhang, M.; Xu, N.; Yang, S.; Dou, J.; Liu, D.; Zhu, L.; Zhu, H.; Hu, J.; Ma, C.; et al. Fine mapping a ClGS gene controlling dark-green stripe rind in watermelon. Sci. Hortic. 2021, 291, 110583.
  35. Tian, S.; Jiang, L.; Gao, Q.; Zhang, J.; Zong, M.; Zhang, H.; Ren, Y.; Guo, S.; Gong, G.; Liu, F.; et al. Efficient CRISPR/Cas9-based gene knockout in watermelon. Plant Cell Rep. 2017, 36, 399–406.
  36. Tian, S.; Jiang, L.; Cui, X.; Zhang, J.; Guo, S.; Li, M.; Zhang, H.; Ren, Y.; Gong, G.; Zong, M.; et al. Engineering herbicide-resistant watermelon variety through CRISPR/Cas9-mediated base-editing. Plant Cell Rep. 2018, 37, 1353–1356.
  37. Zhang, J.; Guo, S.; Ji, G.; Zhao, H.; Sun, H.; Ren, Y.; Tian, S.; Li, M.; Gong, G.; Zhang, H.; et al. A unique chromosome translocation disrupting ClWIP1 leads to gynoecy in watermelon. Plant J. 2019, 101, 265–277.
  38. Wang, Y.; Wang, J.; Guo, S.; Tian, S.; Zhang, J.; Ren, Y.; Li, M.; Gong, G.; Zhang, H.; Xu, Y. CRISPR/Cas9-mediated mutagenesis of ClBG1 decreased seed size and promoted seed germination in watermelon. Hortic. Res. 2021, 8, 70.
  39. Levi, A.; Thies, J.A.; Wechter, W.P.; Harrison, H.F.; Simmons, A.M.; Reddy, U.K.; Nimmakayala, P.; Fei, Z. High frequency oligonucleotides: Targeting active gene (HFO-TAG) markers revealed wide genetic diversity among Citrullus spp. accessions useful for enhancing disease or pest resistance in watermelon cultivars. Genet. Resour. Crop Evol. 2012, 60, 427–440.
  40. Achigan-Dako, E.G.; Avohou, E.S.; Linsoussi, C.; Ahanchede, A.; Vodouhe, R.S.; Blattner, F.R. Phenetic characterization of Citrullus spp. (Cucurbitaceae) and differentiation of egusi-type (C. mucosospermus). Genet. Resour. Crop Evol. 2015, 62, 1159–1179.
  41. Yang, X.; Ren, R.; Ray, R.; Xu, J.; Li, P.; Zhang, M.; Liu, G.; Yao, X.; Kilian, A. Genetic diversity and population structure of core watermelon (Citrullus lanatus) genotypes using DArTseq-based SNPs. Plant Genet. Resour. 2016, 14, 226–233.
  42. Kim, Y.-C.; Choi, D.; Zhang, C.; Liu, H.-F.; Lee, S. Profiling cucurbitacins from diverse watermelons (Citrullus spp.). Hortic. Environ. Biotechnol. 2018, 59, 557–566.
  43. Tannin-Spitz, T.; Bergman, M.; Grossman, S. Cucurbitacin glycosides: Antioxidant and free-radical scavenging activities. Biochem. Biophys. Res. Commun. 2007, 364, 181–186.
  44. Duangmano, S.; Sae-Lim, P.; Suksamrarn, A.; E Domann, F.; Patmasiriwat, P. Cucurbitacin B inhibits human breast cancer cell proliferation through disruption of microtubule polymerization and nucleophosmin/B23 translocation. BMC Complement. Altern. Med. 2012, 12, 185.
  45. Zhang, Z.; Zhang, Y.; Sun, L.; Qiu, G.; Sun, Y.; Zhu, Z.; Luan, F.; Wang, X. Construction of a genetic map for Citrullus lanatus based on CAPS markers and mapping of three qualitative traits. Sci. Hortic. 2018, 233, 532–538.
  46. Gong, C.; Li, B.; Anees, M.; Zhu, H.; Zhao, S.; He, N.; Lu, X.; Liu, W. Fine-mapping reveals that the bHLH gene Cla011508 regulates the bitterness of watermelon fruit. Sci. Hortic. 2021, 292, 110626.
  47. Zhou, Y.; Ma, Y.; Zeng, J.; Duan, L.; Xue, X.; Wang, H.; Lin, T.; Liu, Z.; Zeng, K.; Zhong, Y.; et al. Convergence and divergence of bitterness biosynthesis and regulation in Cucurbitaceae. Nat. Plants 2016, 2, 16183.
  48. Davidovich-Rikanati, R.; Shalev, L.; Baranes, N.; Meir, A.; Itkin, M.; Cohen, S.; Zimbler, K.; Portnoy, V.; Ebizuka, Y.; Shibuya, M.; et al. Recombinant yeast as a functional tool for understanding bitterness and cucurbitacin biosynthesis in watermelon (Citrullus spp). Yeast 2015, 32, 103–114.
  49. Manzano, S.; Martínez, C.; García, J.M.; Megías, Z.; Jamilena, M. Involvement of ethylene in sex expression and female flower development in watermelon (Citrullus lanatus). Plant Physiol. Biochem. 2014, 85, 96–104.
  50. Aguado, E.; García, A.; Manzano, S.; Valenzuela, J.L.; Cuevas, J.; Pinillos, V.; Jamilena, M. The sex-determining gene CitACS4 is a pleiotropic regulator of flower and fruit development in watermelon (Citrullus lanatus). Plant Reprod. 2018, 31, 411–426.
  51. Manzano, S.; Aguado, E.; Martínez, C.; Megías, Z.; García, A.; Jamilena, M. The ethylene biosynthesis gene CitACS4 regulates monoecy/andromonoecy in watermelon (Citrullus lanatus). PLoS ONE 2016, 11, e0154362.
  52. Aguado, E.; García, A.; Iglesias-Moya, J.; Romero, J.; Wehner, T.C.; Gómez-Guillamón, M.L.; Pico, M.B.; Garces-Claver, A.; Martínez, C.; Jamilena, M. Mapping a partial andromonoecy locus in Citrullus lanatus using BSA-seq and GWAS approaches. Front. Plant Sci. 2020, 11, 1243.
  53. Zhu, Y.C.; Yuan, G.P.; Jia, S.F.; An, G.L.; Li, W.H.; Sun, D.X.; Liu, J.P. Transcriptomic profiling of watermelon (Citrullus lanatus) provides insights into male flowers development. J. Integr. Agric 2022, 21, 407–421.
  54. Rhee, S.-J.; Seo, M.; Jang, Y.-J.; Cho, S.; Lee, G.P. Transcriptome profiling of differentially expressed genes in floral buds and flowers of male sterile and fertile lines in watermelon. BMC Genom. 2015, 16, 914.
  55. Zhang, R.; Chang, J.; Li, J.; Lan, G.; Xuan, C.; Li, H.; Ma, J.; Zhang, Y.; Yang, J.; Tian, S.; et al. Disruption of the bHLH transcription factor Abnormal Tapetum 1 causes male sterility in watermelon. Hortic. Res. 2021, 8, 258.
  56. Yi, L.; Wang, Y.; Wang, F.; Song, Z.; Li, J.; Gong, Y.; Dai, Z. Comparative transcriptome analysis reveals the molecular mechanisms underlying male sterility in autotetraploid watermelon. J. Plant Growth Regul. 2022.
  57. Solmaz, I.; Sarı, N. Characterization of watermelon (Citrullus lanatus) accessions collected from Turkey for morphological traits. Genet. Resour. Crop Evol. 2009, 56, 173–188.
  58. Szamosi, C.; Solmaz, I.; Sari, N.; Bársony, C. Morphological characterization of Hungarian and Turkish watermelon (Citrullus lanatus (Thunb.) Matsum. et Nakai) genetic resources. Genet. Resour. Crop Evol. 2009, 56, 1091–1105.
  59. Elbekkay, M.; Hamza, H.; Neily, M.H.; Djebali, N.; Ferchichi, A. Characterization of watermelon local cultivars from Southern Tunisia using morphological traits and molecular markers. Euphytica 2021, 217, 74–89.
  60. Dong, W.; Wu, D.; Li, G.; Wu, D.; Wang, Z. Next-generation sequencing from bulked segregant analysis identifies a dwarfism gene in watermelon. Sci. Rep. 2018, 8, 2908.
  61. Jang, Y.J.; Yun, H.S.; Rhee, S.-J.; Seo, M.; Kim, Y.; Lee, G.P. Exploring molecular markers and candidate genes responsible for watermelon dwarfism. Hortic. Environ. Biotechnol. 2020, 61, 173–182.
  62. Zhang, T.; Liu, J.; Amanullah, S.; Ding, Z.; Cui, H.; Luan, F.; Gao, P. Fine mapping of Cla015407 controlling plant height in watermelon. J. Am. Soc. Hortic. Sci. 2021, 146, 196–205.
  63. Wei, C.; Zhu, C.; Yang, L.; Zhao, W.; Ma, R.; Li, H.; Zhang, Y.; Ma, J.; Yang, J.; Zhang, X. A point mutation resulting in a 13 bp deletion in the coding sequence of Cldf leads to a GA-deficient dwarf phenotype in watermelon. Hortic. Res. 2019, 6, 132.
  64. Zhu, H.; Zhang, M.; Sun, S.; Yang, S.; Li, J.; Li, H.; Yang, H.; Zhang, K.; Hu, J.; Liu, D.; et al. A single nucleotide deletion in an ABC transporter gene leads to a dwarf phenotype in watermelon. Front. Plant Sci. 2019, 10, 1399.
  65. Li, Y.; Xu, A.; Dong, W.; Li, Z.; Li, G. Genetic analysis of a dwarf vine and small fruit watermelon mutant. Hortic. Plant J. 2016, 2, 224–228.
  66. Cho, Y.; Lee, S.; Park, J.; Kwon, S.; Park, G.; Kim, H.; Park, Y. Identification of a candidate gene controlling semi-dwarfism in watermelon, Citrullus lanatus, using a combination of genetic linkage mapping and QTL-seq. Hortic. Environ. Biotechnol. 2021, 62, 447–459.
  67. Dou, J.; Yang, H.; Sun, D.; Yang, S.; Sun, S.; Zhao, S.; Lu, X.; Zhu, H.; Liu, D.; Ma, C.; et al. The branchless gene Clbl in watermelon encoding a TERMINAL FLOWER 1 protein regulates the number of lateral branches. Theor. Appl. Genet. 2021, 135, 65–79.
  68. McGregor, C.; Waters, V. Flowering patterns of pollenizer and triploid watermelon cultivars. HortScience 2014, 49, 714–721.
  69. Stone, S.; Boyhan, G.; McGregor, C. Inter- and intracultivar variation of heirloom and open-pollinated watermelon cultivars. HortScience 2019, 54, 212–220.
  70. Karaca, F.; Yetişir, H.; Solmaz, I.; Çandir, E.; Kurt, Ş.; Sari, N.; Güler, Z. Rootstock potential of Turkish Lagenaria siceraria germplasm for watermelon: Plant growth, yield and quality. Turk. J. Agric. For. 2012, 36, 167–177.
  71. Singh, D.; Singh, R.; Sandhu, J.S.; Chunneja, P. Morphological and genetic diversity analysis of Citrullus landraces from India and their genetic inter relationship with continental watermelons. Sci. Hortic. 2017, 218, 240–248.
  72. Cheng, Y.; Luan, F.; Wang, X.; Gao, P.; Zhu, Z.; Liu, S.; Baloch, A.M.; Zhang, Y. Construction of a genetic linkage map of watermelon (Citrullus lanatus) using CAPS and SSR markers and QTL analysis for fruit quality traits. Sci. Hortic. 2016, 202, 25–31.
  73. Freeman, J.H.; Miller, G.; Olson, S.; Stall, W. Diploid watermelon pollenizer cultivars differ with respect to triploid watermelon yield. HortTechnology 2007, 17, 518–522.
  74. Dittmar, P.J.; Monks, D.W.; Schultheis, J.R. Maximum potential vegetative and floral production and fruit characteristics of watermelon pollenizers. HortScience 2009, 44, 59–63.
  75. Dittmar, P.J.; Monks, D.W.; Schultheis, J.R. Use of commercially available pollenizers for optimizing triploid watermelon production. HortScience 2010, 45, 541–545.
  76. Garantonakis, N.; Varikou, K.; Birouraki, A.; Edwards, M.; Kalliakaki, V.; Andrinopoulos, F. Comparing the pollination services of honey bees and wild bees in a watermelon field. Sci. Hortic. 2016, 204, 138–144.
  77. Kombo, M.D.; Sari, N. Rootstock effects on seed yield and quality in watermelon. Hortic. Environ. Biotechnol. 2019, 60, 303–312.
  78. Dia, M.; Wehner, T.C.; Hassell, R.; Price, D.S.; Boyhan, G.E.; Olson, S.; King, S.; Davis, A.R.; Tolla, G.E. Genotype × environment interaction and stability analysis for watermelon fruit yield in the United States. Crop Sci. 2016, 56, 1645–1661.
  79. Gong, C.; Zhao, S.; Yang, D.; Lu, X.; Anees, M.; He, N.; Zhu, H.; Zhao, Y.; Liu, W. Genome-wide association analysis provides molecular insights into natural variation in watermelon seed size. Hortic. Res. 2022, 9, 74.
More
Information
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : , , ,
View Times: 348
Revisions: 2 times (View History)
Update Date: 21 Jul 2022
1000/1000