Mini Review ARTICLE
Translating the “Banana Genome” to Delineate Stress Resistance, Dwarfing, Parthenocarpy and Mechanisms of Fruit Ripening
- ICAR-National Research Centre on Plant Biotechnology, New Delhi, India
Evolutionary frozen, genetically sterile and globally iconic fruit “Banana” remained untouched by the green revolution and, as of today, researchers face intrinsic impediments for its varietal improvement. Recently, this wonder crop entered the genomics era with decoding of structural genome of double haploid Pahang (AA genome constitution) genotype of Musa acuminata. Its complex genome decoded by hybrid sequencing strategies revealed panoply of genes and transcription factors involved in the process of sucrose conversion that imparts sweetness to its fruit. Historically, banana has faced the wrath of pandemic bacterial, fungal, and viral diseases and multitude of abiotic stresses that has ruined the livelihood of small/marginal farmers’ and destroyed commercial plantations. Decoding structural genome of this climacteric fruit has given impetus to a deeper understanding of the repertoire of genes involved in disease resistance, understanding the mechanism of dwarfing to develop an ideal plant type, unraveling the process of parthenocarpy, and fruit ripening for better fruit quality. Further, injunction of comparative genomics will usher in integration of information from its decoded genome and other monocots into field applications in banana related but not limited to yield enhancement, food security, livelihood assurance, and energy sustainability. In this mini review, we discuss pre- and post-genomic discoveries and highlight accomplishments in structural genomics, genetic engineering and forward genetic accomplishments with an aim to target genes and transcription factors for translational research in banana.
Banana is a unique and iconic fruit among global consumers. The fruit has numerous health benefits such as subsiding appetite, sugar craving, fighting obesity, improving muscle endurance, and reducing bad cholesterol in humans. Along with its related clade plantain, it is grown as a cash crop1 around the world with more than 85% for local consumption (Sharrock and Frison, 1998). Predominantly, it is cultivated in tropical and sub-tropical countries (van Asten et al., 2011) and is an important source of livelihood of marginal farmers of Asia and South-east Asia (Figure 1a,b,c) (Sreedharan et al., 2013). It ranks second to mango as the most consumed fruit in the world and is a source of food security in many developing countries (Martin et al., 2013). This fruit has a unique yellow peel and sweet flesh which makes it popular as a part of healthy diet in industrialized countries as well. The canoe shaped fruit is usually fried, roasted, or boiled when green, while special fruit types of the East African highland plantain cultivar are preferentially brewed. It ranks next to rice, wheat and maize (Perrier et al., 2011) in terms of its importance as source of staple starch with global annual production of 106 MT in which Asia contributes 60 MT (WBF: Statistics and data, 2012).
FIGURE 1. Banana cultivation is one of the major land uses in Asia and Africa not only for nutritional requirement but also a key household source of income for marginal farmers. The banana genome sequence, comprising a high-resolution map of genes, repetitive elements and variation (single-nucleotide polymorphisms, INDELs) will be leveraged by researchers/breeders to construct high-density, well-placed marker sets. Further, marker-assisted selection will allow breeders to sort through thousands of recombinants to select plant type that contain only the beneficial gene(s) and remove linkage drag. (a) A commercial banana plantation in northwest India. (b) Single bunch of banana is handpicked and carefully washed to minimize the bruises and marketable loss to the fingers. (c) Harvest-mature looms are transported for ripening to nearby banana industry depicting intricate association of livelihood for farmers, traders, distributors, and industry. (d) Origin and distribution of bananas representing primary center of origin () that geographically overlaps from northeast India, Thailand, Myanmar, Bangladesh to other Polynesian regions and secondary center of diversity covering peninsular Malaysia and Indonesia. (e) A banana plantation devastated by Panama wilt caused by Fusarium oxysporum sp. cubense race 4. (f) Typical leaf-spot symptoms of black sigatoka disease in young leaves of banana caused by Mycosphaerella fijiensis. Source: (d–f) from Google (www.google.com).
Banana Biology, Origin and Evolution
Taxonomically, bananas and plantains are monocotyledonous plants in the genus Musa (Family: Musaceae; Order: Zingiberales) that comprises “Eumusa” with 22 chromosomes and “Australimusa” with 20 chromosome sets (Perrier et al., 2009, 2011). Though, botanically it is a monocotyledonous perennial herb (Uma et al., 2008), the presence of the unique tall order pseudo-stem apparently attributes it the tree phenotype (approximately 2.0–3.5 m). However, absence of typical traits of tree stems such as lignification and secondary thickening of the pseudo-stem differentiates them from trees (Wu et al., 2016).
Banana is considered to have originated in Asiatic region (Simmonds, 1962) with South-east Asia covering India to Polynesia as the primary center of origin; while the tropical rainforest of Malaysia–Indonesia is considered as the center of diversity with occurrence of diverse endemic wild banana species (Figure 1d). As per the International Classification System (ICS) Musa has five major sections, viz., Eumusa, Rhodochlamys, Callimusa, Australimusa and Incertae sedis. Of these sections, Eumusa contributes to the wide diversity for wild and cultivated types. There are 11 wild species reported across the globe of which six species are prevalent in India. M. acuminata and M. balbisiana are the major progenitors of present day bananas and have a wider distribution throughout the banana growing states including Andaman and Nicobar Islands.
Plantains and bananas (Musa spp. section Eumusa) originated from intra and inter-specific hybridization between two wild species namely M. acuminata Colla (A genome) and M. balbisiana Colla (B genome). Polyploidy and hybridization have given rise to a number of diploid, triploid, and tetraploid clones with different combinations of A and B genomes like AA, AB, AAA, AAB, ABB, AABB, AAAB, ABBB (Saraswathi, 2011; Vanhove et al., 2012; Davey, 2013). Dessert and highland bananas are classified mainly as AAA, plantains are AAB, and cooking bananas are ABB. The first and most crucial step in evolution of edible bananas was the development and selection for parthenocarpy and seed sterility in M. acuminata, giving rise to the edible diploid (AA) cultivars. It is believed that chromosome restitution at meiosis in M. acuminata gave rise to edible triploid AAA (acuminata) bananas. Though not clear, using variation in anthocyanin pigments as a marker, it is assumed that three different subspecies such as malaccensis, banksii, and zebrina (Horry and Jay, 1990) were involved in the evolution of triploid edible bananas.
Banana Diversity and Use
Till 1970, the delicious ‘Gros’ Michel or ‘Big Mike’ bananas were the globally accepted varieties for consumption. However, after out-break of the “Panama disease,” they were replaced by the yellow Cavendish variety (Heslop-Harrison and Schwarzacher, 2007) which were resistant to Panama wilt. Currently, more than 90% of the bananas sold in the market are of Cavendish type. ‘Robusta’ (AAA), a Cavendish cultivar of banana, ripens without changing to yellow (green ripe) and has good shelf-life with mild taste and mushy texture of typical Cavendish. ‘Nendran’ type banana (AAB) is preferred for cooking and making chips while ‘Peyan’ (ABB) is a dessert banana. ‘Poovan’ (AAB) and ‘Njalipoovan’ are sweet dessert banana with small fingers, thin skin and delicate flavor but exhibit poor keeping quality thus reducing the marketable value. Currently, a handful of other prized types are available such as ‘red’ (AAA) - a delicious banana that has a sweet taste and creamy texture. The ‘Burro’ varieties grown in Mexico have a sweet-and-sour taste but are stubbier and fatter than the Cavendish type. ‘Manzano’ variety is native to Central and South America and possesses a firmer texture than Cavendish with complex scent and taste, marked by a strong tart-apple aroma that gives sweetness after chewing. Another variety named as ‘Baby’ for their miniature size (Malaysian origin) and is sweet in taste after complete ripening. A different clade called ‘Plantain’ is usually cooked for consumption and serves as an economical but delicious substitute for potatoes/rice in Latin American cuisines.
Genetically, banana is a triploid crop and comprises of both A (M. acuminata) and B (M. balbisiana) genomes. The triploid genetic constitution of banana posed a huge challenge to the sequencing and assembly of its genome. Therefore, a double haploid (PH-Pahang) M. acuminata was generated and sequencing was accomplished in 2012 by a team of researchers (D’Hont et al., 2012) under the framework of Global Musa Genomics Consortium. The genome size of Musa ranges from 554 megabase (Mb) in M. balbisiana to 523 Mb in M. acuminata. The genome is two/three times larger than the genomes of cultivated rice (Oryza sativa, 250 Mb) or Arabidopsis (150 Mb) but still is much smaller than the Triticeae cereals such as wheat (17,000 Mb), barley (5,500 Mb) and rye (9000 Mb; D’Hont et al., 2012). Nonetheless, the 523 Mb genome of banana was precisely sequenced with a combination of Sanger, 454 and Illumina technologies and 90% assembled into 7000 scaffolds with contiguity on par with other plant genomes (1.3 Mb scaffold N50). Further, 70% of the assembly anchored to 11 Pahang chromosomes with 250 scaffolds covering 92% of the annotated genes. Sequencing information further revealed that banana genome contained approximately 36,000 genes which were mostly located in the distal-end of the chromosomes. It was also observed that like most plant genomes (Singh et al., 2012; Varshney et al., 2012; Wang et al., 2012), the Musa genome consists of repetitive DNA (about 50%) comprising of transposable elements.
Interestingly, the number of transcription factors (TFs) identified in Musa (3,155) is highest among all sequenced plants. Of these, 759 TFs were specific to banana and belonged to the MYB and AP2/ERF transcription factor families that plays a role in fruit architecture and ripening (D’Hont et al., 2012). Expression profiling study in response to ethylene treatment identified a cassette of transcription factors (597) speculated to contribute to the unique climacteric character of ripening in banana. Genes encoding cell-wall modifying enzymes and β-amylase were found to be up-regulated in contrast to three starch synthase genes which were down regulated during ripening. In addition, two vacuolar invertase genes involved in sucrose conversion, work in reverse tandem to maintain soluble sugar homeostasis that imparts sweetness to ripening bananas.
Disease Epidemics and Resistance in Cultivated Banana
Cultivated bananas are propagated through vegetative suckers and this clonal method of propagation makes banana particularly vulnerable to diseases. Historically, Panama disease (Figure 1e) caused by the fungus Fusarium oxysporum sp. cubense has inflicted major devastation to the banana plantations (Moore et al., 1995). A virulent form of this pathogen, ‘Tropical Race 4,’ has caused substantial losses in Asia and other regions of the world to both subsistence farmers and commercial growers (Hwang and Ko, 2004). Exploring for genetic resistance in banana germplasm has led to the identification of a number of varieties (Ortiz, 1995) that could be potentially utilized as resistance gene donors for breeding or gene transfer programs. However, the genetically sterile nature of banana is an impediment to resistance breeding. Therefore, utilizing forward genetics tool of induced mutagenesis, a resistant cultivar of Rasthali (Silk, AAB) has been developed to combat fusarium wilt (Saraswathi et al., 2016). The putative resistant plants showed promising results with completely clean corm (disease score 1) that had no vascular discoloration (zero disease manifestation). Further, the double haploid Pahang, used for genome sequencing, was found to be highly resistant to F. oxysporum race-4. Functional genomics studies on Pahang would unravel the genes underlying this inherent resistance.
Another fungal disease of banana which has acquired importance is black Sigatoka leaf spot disease (Figure 1f), caused by Mycosphaerella fijiensis which results in more than 50% crop losses (Ferreira and Silva, 2004). A triple gene construct from heterologous sources viz.(i) endochitinase gene ThEn-42 from Trichoderma harzianum, (ii) grape stilbene synthase (StSy), and (iii) superoxide dismutase Cu, Zn-SOD from tomato were used to transform Grand Nain banana (Vishnevetsky et al., 2011). Repeated field trials of this transgenic exhibited tolerance not only to Sigatoka but also to ‘Gray mold/ blossom blight’ – another fungal disease of banana caused by Botrytis cinerea.
Viruses form a minority amongst the pathogens aﬄicting banana (Hull, 2002). However, banana streak virus (BSV) formed an extreme case of parasitism before its genome sequence uncovered the molecular facts. Genome sequence assembly data allocated the endogenous viral sequences integrated at 24 loci spanning 10 chromosomes in Pahang genome. Molecular characterization identified them to belong to badnavirus group that differed from the endogenous BSV species (eBSV) found in M. Balbisiana, which are known to be capable of vertical transmission. Further, it was observed that these viral sequences in banana genome have lost their original form and integrity and, therefore, can not seemingly form free infectious particles leading to disease. Conclusion from recent genomic study refuted the earlier understanding that integrated viral elements in banana genome are capable of expression and can give rise to de novo viral infection (Harper et al., 2002; Iskra-Caruana et al., 2010) leading to disease pandemism.
Mechanism of Dwarfing in Banana
Commercially cultivated bananas are tall order plants measuring more than two meter in height. The taller canopy makes them vulnerable to high velocity wind, low/high cyclonic typhoons that break the pseudo-stem and ushers irreparable loss to commercial plantations. Therefore, dwarf variety of banana is the desirable ideotype to reap the advantages of efficient agronomic procedures like high density planting and timely cultural practices. Genetically, it has been shown that dwarfism in plants is associated with the reduction of bio-available gibberellic acid (GA). The famous high-yielding semi-dwarf variety of rice (IR8) which ushered in the ‘Green Revolution’ was accomplished due to a mutation in the sd1 gene. This gene is involved in the biosynthesis of gibberellin and the mutation attenuates the GA biosynthesis there by making the rice plant semi-dwarf. Thus, identification of dwarfism related genes in banana was of paramount importance. Recently, a mutant of ‘Williams’ variety of banana was developed (Chen et al., 2016) that exhibited reduced height (approximately 1.7 m) and their pseudo-stem showed better mechanical strength compared to its progenitor. Using the information from banana genome, it was elucidated that gibberellic acid plays a pivotal role in its dwarfism. Genome-wide screening using contrasting banana genotypes further revealed that 36 genes are involved in GA metabolism in banana. While dwarf banana had differential expression of genes involved in GA homeostasis, the young fruits were observed to be the sites of GA metabolism that contribute to fruit length. Identification of GA metabolism genes will expedite application of molecular techniques such as CRISPR/CAS9 (Cong et al., 2013; Li et al., 2013) to tinker GA homeostasis to develop dwarf banana.
Banana garners huge demand in human consumption due to its seedless fleshy fruit. The ability of plants to bear seed-less fruit (without pollination and fertilization) is due to the phenomenon known as “Parthenocarpy.” Additionally, female sterility is also hypothesized to be the cause of parthenocarpy in many fruits including banana (Dodds and Simmonds, 1948; Simmonds, 1953, 1962). Parthenocarpy in banana is believed to be the manifestation of A genome (Simmonds, 1962). Growth promoting phytohormones such as auxins, gibberellins, cytokinins and absiscic acid are also reported to be involved in parthenocarpy in melon (Talon et al., 1992) and tomato (Fos et al., 2000; Ding et al., 2013). Though intrinsic mechanism of natural parthenocarpy in plants is still unresolved, it is observed that natural parthenocarpic fruits such as banana (Khalifah, 1966) and mandarin (Talon et al., 1990, 1992) record increase in auxin and gibberellins level while levels of ABA declines (Talon et al., 1990). Genetically, parthenocarpy may happen due to a single partially dominant gene as in cucurbits (Kim et al., 1992; Menezes et al., 2005) or due to a single recessive gene as in sweet pepper (Tiwari et al., 2011) or due pleiotropy of major and minor genes as in brinjal/eggplant (Miyatake et al., 2012). In case of banana, parthenocarpy is hypothesized (Sardos et al., 2016) to be due to a major dominant gene (P or P1) interacting with minor ones (Simmonds, 1953). With decoding of structural genome of banana, discovery of the precise mechanism of parthenocarpy will give a boost to quality fruit production in commercial plantation.
Ripening in fruits is a natural phenomenon by which they taste sweeter and gain palatability. Biochemically, it begins with concomitant increase in acidity till a level (brix-acid ratio) when fruits taste/smell tarter. Being a climacteric fruit, ripening in banana is an important phenological event. Edible cultivated bananas are triploids with AAA, AAB and ABB genomic composition of which the A-genome (M. balbisiana) has been associated with banana pre-harvest development and post-harvest ripening (Davey, 2013). Cultivars possessing more of A-genome exhibit high yield, long fingers, and long-term storage (Hu et al., 2015) an attribute of best fruit quality. Post-genomic research has strongly indicated role of the bZIP transcription factors in fruit development process in many crops (Levi et al., 2006; Costa and Alba, 2010; Rohrmann et al., 2011). Recently, extensive involvement of bZIPs and WRKY in fruit development and post-harvest ripening has been demonstrated (Goel et al., 2016; Hu et al., 2016a) by comparing its expression pattern at different stages of banana development. The high expression levels of MabZIPs in fruit developmental and ripening is postulated to control the fruit quality of banana. Another transcription factor MaDEAR1 (repressor) is reported to be negatively involved in cell wall modification and softening of banana (Fan et al., 2016). With development of suitable transformation/regeneration techniques (Uma et al., 2011, 2012) these TFs will be targets of modulation in banana for best quality looms.
Abiotic Stress Tolerance
Due to inherent rapid rate of growth, shallow root system and permanent green canopy, banana requires abundant supply of water (van Asten et al., 2011) for optimum yield potential. The B-genome of banana has been the target for breeding programs (Davey, 2013; Hu et al., 2015) as it imparts intrinsic tolerances to both biotic and abiotic stresses. In M. balbisiana the B-genome imparts (i) resistance to infection of Xanthomonas and (ii) tolerance to drought/water stress (Tripathi et al., 2007; Vanhove et al., 2012; Davey, 2013). At molecular level, it has been reported that multiple bZIP transcription factors are involved in imparting tolerance against cold, drought and salt stress in banana (van Asten et al., 2011), beans (Rodriguez-Uribe and O’Connell, 2006), brachypodium (Liu and Chu, 2015) and rice (Liu et al., 2012). In fact, the cultivars containing the B-genome has been reported to exhibit higher tolerance to abiotic stresses (Hu et al., 2015). Gene expression analysis in banana showed 74% bZIP genes had increased transcription levels under cold, drought, and salt stresses. Commensurate increase in transcription levels was also observed in other plants such as cassava (Hu et al., 2016b), Brachypodium distachyon (Liu and Chu, 2015) and maize (Wei et al., 2012). Post-genomic discovery of bZIPs (Hu et al., 2016a), microRNAs (Chai et al., 2015) along with key metabolites (Pandey et al., 2016) is expected to expedite the molecular breeding process by ushering in, understanding the role, these transcription factors in signal transduction, developmental processes and responses to abiotic stress in banana.
Conclusion and Future Perspective
Banana has remained practically untouched by the ‘Green Revolution’ because of the difficulties encountered in conventional breeding programs in this genetically sterile triploid crop. Inter alia, being the most consumed fruit banana has immense capability to contribute to food security through higher and stable yields. It has been a challenge for banana breeders to produce disease resistant polyploid hybrids through genetic recombination. Like other crops (Dash et al., 2014), availability of structural genome information has opened up vistas to saturate the genome with molecular markers which would enable banana researchers to select good plant type at an early stage in commercial plantation. Structural genomics of banana has further delineated molecular mechanisms of dwarfing, imparting disease resistance, role of phyto-hormones in parthenocarpy and pivotal role of transcription factors in formation of this iconic fruit. Now, it will provide impetus to Musa researchers to apply functional genomics and comparative genome analysis to identify, clone, and characterize genes responsible for key agronomic traits as well as biotic and abiotic stress tolerance. As of today, the mechanism of action and the inter-connection of various signaling cascades remain largely unknown in banana. Functional analysis to unravel regulatory details small-, micro-, and si-RNAs and their role in the stress responses and hormone signaling will provide useful information for translational research in banana. As our molecular understanding advances, biotechnological interventions such as gene discovery, genetic engineering, targeted transformation/regeneration, and progressive bioinformatic tools (Martin et al., 2016) coupled with validated markers (Backiyarani et al., 2013) will accelerate breeding and super-domestication of banana will be a reality soon.
PD planned, collected information, organized, and prepared the manuscript. RR designed and contributed for writing and reviewing the manuscript.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
We thank Dr. Todd P. Michael, Monsanto (USA) and Dr. Rohini Sreevathsa for giving initial input and critical reading of the MS. We sincerely apologize to those researchers whose work could not be cited due to space limitations.
Backiyarani, S., Uma, S., Varathraja, P., and Saraswathi, M. (2013). Mining of EST-SSR markers of Musa and their transferability studies among the members of order the Zingiberales. Appl. Biochem. Biotechnol. 169, 228–238.
Chai, J., Feng, R., Shi, H., Ren, M., Zhang, Y., and Wang, J. (2015). Bioinformatic identification and expression analysis of banana microRNAs and their targets. PLoS ONE 10:e0123083. doi: 10.1371/journal.pone.0123083
Chen, J., Xie, J., Duan, Y., Hu, H., Hu, Y., and Li, W. (2016). Genome-wide identification and expression profiling reveal tissue-specific expression and differentially-regulated genes involved in gibberellin metabolism between Williams banana and its dwarf mutant. BMC Plant Biol. 16:123. doi: 10.1186/s12870-016-0809-1
Costa, F., and Alba, R. (2010). Use of homologous and heterologous gene expression profiling tools to characterize transcription dynamics during apple fruit maturation and ripening. BMC Plant Biol. 10:229.
Dash, P. K., Cao, Y., Jailani, A. K., Gupta, P., Venglat, P., Xiang, D., et al. (2014). Genome-wide analysis of drought induced gene expression changes in flax (Linum usitatissimum). GM Crops Food 5, 106–119.
D’Hont, A., Denoeud, F., Aury, J.-M., Baurens, F.-C., Carreel, F., Garsmeur, O., et al. (2012). The banana (Musa acuminata) genome and the evolution of monocotyledonous plants. Nature 488, 213–217. doi: 10.1038/nature11241
Ding, J., Chen, B., Xia, X., Mao, W., Shi, K., Zhou, Y., et al. (2013). Cytokinin-induced parthenocarpic fruit development in tomato is partly dependent on enhanced gibberellin and auxin biosynthesis. PLoS ONE 8:e70080. doi: 10.1371/journal.pone.0070080
Fan, Z., Kuang, J., Fu, C., Shan, W., Han, Y., Xiao, Y., et al. (2016). The banana transcriptional repressor MaDEAR1 negatively regulates cell wall-modifying genes involved in fruit Ripening. Front. Plant Sci. 7:1201. doi: 10.3389/fpls.2016.01021
Goel, R., Pandey, A., Trivedi, P. K., and Asif, M. H. (2016). Genome-wide analysis of the Musa WRKY gene family: evolution and differential expression during development and stress. Front. Plant Sci. 7:299. doi: 10.3389/fpls.2016.00299
Horry, J. P., and Jay, M. (1990). “An evolutionary background of bananas as deduced from flavonoids diversification in Identification of genetic diversity in the genus,” in Proceedings of an International Workshop, Los Banos, Philippines, ed. R. L. Jarret (Montpellier: INIBAP), 5–10.
Hu, W., Wang, L., Tie, W., Yan, Y., Ding, Z., Liu, J., et al. (2016a). Genome-wide analyses of the bZIP family reveal their involvement in the development, ripening and abiotic stress response in banana. Sci. Rep. 6:30203. doi: 10.1038/srep30203
Hu, W., Yang, H., Yan, Y., Wei, Y., Tie, W., Ding, Z., et al. (2016b). Genome-wide characterization and analysis of bZIP transcription factor gene family related to abiotic stress in cassava. Sci. Rep. 6:22783. doi: 10.1038/srep22783
Hu, W., Zuo, J., Hou, X., Yan, Y., Wei, Y., Liu, J., et al. (2015). The auxin response factor gene family in banana: genome-wide identification and expression analyses during development, ripening, and abiotic stress. Front. Plant Sci. 6:742. doi: 10.3389/fpls.2015.00742
Kim, I. S., Okubo, H., and Fujieda, K. (1992). Endogenous levels of IAA in relation to parthenocarpy in cucumber (Cucumis sativus L.). Sci. Hortic. (Amsterdam) 52, 1–8. doi: 10.1016/0304-4238(92)90002-T
Levi, A., Davis, A., Hernandez, A., Wechter, P., Thimmapuram, J., Trebitsh, T., et al. (2006). Genes expressed during the development and ripening of watermelon fruit. Plant Cell Rep. 25, 1233–1245. doi: 10.1007/s00299-006-0163-0
Li, J.-F., Norville, J. E., Aach, J., McCormack, M., Zhang, D., Bush, J., et al. (2013). Multiplex and homologous recombination-mediated genome editing in Arabidopsis and Nicotiana benthamiana using guide RNA and Cas9. Nat. Biotechnol. 31, 688–691. doi: 10.1038/nbt.2654
Liu, C., Wu, Y., and Wang, X. (2012). bZIP transcription factor OsbZIP52/RISBZ5: a potential negative regulator of cold and drought stress response in rice. Planta 235, 1157–1169. doi: 10.1007/s00425-011-1564-z
Liu, X., and Chu, Z. (2015). Genome-wide evolutionary characterization and analysis of bZIP transcription factors and their expression profiles in response to multiple abiotic stresses in Brachypodium distachyon. BMC Genomics 16:227. doi: 10.1186/s12864-015-1457-9
Martin, G., Baurens, F.-C., Cardi, C., Aury, J.-M., and D’Hont, A. (2013). The complete chloroplast genome of banana (Musa acuminata, Zingiberales): insight into plastid monocotyledon evolution. PLoS ONE 8:e67350. doi: 10.1371/journal.pone.0067350
Martin, G., Baurens, F.-C., Droc, G., Rouard, M., Cenci, A., Kilian, A., et al. (2016). Improvement of the banana “Musa acuminata” reference sequence using NGS data and semi-automated bioinformatics methods. BMC Genomics 17:243. doi: 10.1186/s12864-016-2579-4
Menezes, C. B., de Maluf, W. R., Azevedo, S. M., de Faria, M. V., Nascimento, I. R., Nogueira, D. W., et al. (2005). Inheritance of parthenocarpy in summer squash (Cucurbita pepo L.). Genet. Mol. Res. 4, 39–46.
Miyatake, K., Saito, T., Negoro, S., Yamaguchi, H., Nunome, T., Ohyama, A., et al. (2012). Development of selective markers linked to a major QTL for parthenocarpy in eggplant (Solanum melongena L.). Theor. Appl. Genet. 124, 1403–1413. doi: 10.1007/s00122-012-1796-8
Pandey, A., Alok, A., Lakhwani, D., Singh, J., Asif, M. H., and Trivedi, P. K. (2016). Genome-wide expression analysis and metabolite profiling elucidate transcriptional regulation of flavonoid biosynthesis and modulation under abiotic stresses in banana. Sci. Rep. 6:31361. doi: 10.1038/srep31361
Perrier, X., Bakry, F., Carreel, F., Jenny, C., Horry, J.-P., Lebot, V., et al. (2009). Combining biological approaches to shed light on the evolution of edible bananas. Ethnobot. Res. Appl. 7, 199–216.
Perrier, X., De Langhe, E., Donohue, M., Lentfer, C., Vrydaghs, L., Bakry, F., et al. (2011). Multidisciplinary perspectives on banana (Musa spp.) domestication. Proc. Natl. Acad. Sci. U.S.A. 108, 11311–11318. doi: 10.1073/pnas.1102001108
Rodriguez-Uribe, L., and O’Connell, M. A. (2006). A root-specific bZIP transcription factor is responsive to water deficit stress in tepary bean (Phaseolus acutifolius) and common bean (P. vulgaris). J. Exp. Bot. 57, 1391–1398. doi: 10.1093/jxb/erj118
Rohrmann, J., Tohge, T., Alba, R., Osorio, S., Caldana, C., McQuinn, R., et al. (2011). Combined transcription factor profiling, microarray analysis and metabolite profiling reveals the transcriptional control of metabolic shifts occurring during tomato fruit development. Plant J. 68, 999–1013. doi: 10.1111/j.1365-313X.2011.04750.x
Saraswathi, M. S., Kannan, G., Uma, S., Thangavelu, R., and Backiyarani, S. (2016). Improvement of banana cv. Rasthali (Silk, AAB) against Fusarium oxysporum f.sp. cubense (VCG 0124/5) through induced mutagenesis: determination of LD50 specific to mutagen, explants, toxins and in vitro and in vivo screening for Fusarium wilt resistance. Indian J. Exp. Biol. 54, 345–353.
Sardos, J., Rouard, M., Hueber, Y., Cenci, A., Hyma, K. E., Van Den Houwe, I., et al. (2016). A genome-wide association study on the seedless phenotype in banana (Musa spp.) reveals the potential of a selected panel to detect candidate genes in a vegetatively propagated crop. PLoS ONE 11:e01. doi: 10.1371/journal.pone.0154448
Singh, N. K., Gupta, D. K., Jayaswal, P. K., Mahato, A. K., Dutta, S., Singh, S., et al. (2012). The first draft of the pigeonpea genome sequence. J. Plant Biochem. Biotechnol. 21, 98–112. doi: 10.1007/s13562-011-0088-8
Sreedharan, S., Shekhawat, U. K. S., and Ganapathi, T. R. (2013). Transgenic banana plants overexpressing a native plasma membrane aquaporin MusaPIP1;2 display high tolerance levels to different abiotic stresses. Plant Biotechnol. J. 11, 942–952. doi: 10.1111/pbi.12086
Talon, M., Zacarias, L., and Primo-Millo, E. (1990). Hormonal changes associated with fruit set and development in mandarins differing in their parthenocarpic ability. Physiol. Plant. 79, 400–406. doi: 10.1111/j.1399-3054.1990.tb06759.x
Tiwari, A., Vivian-Smith, A., Voorrips, R. E., Habets, M. E. J., Xue, L. B., Offringa, R., et al. (2011). Parthenocarpic potential in Capsicum annuum L. is enhanced by carpelloid structures and controlled by a single recessive gene. BMC Plant Biol. 11:143. doi: 10.1186/1471-2229-11-143
Tripathi, L., Odipio, J., Tripathi, J. N., and Tusiime, G. (2007). A rapid technique for screening banana cultivars for resistance to Xanthomonas wilt. Eur. J. Plant Pathol. 121, 9–19. doi: 10.1007/s10658-007-9235-4
Uma, S., Lakshmi, S., and Saraswathi, M. (2012). Plant regeneration through somatic embryogenesis from immature and mature zygotic embryos of Musa acuminata ssp. burmannica. Invitr. Cell. Dev. Biol. Plant. 48, 539–545.
Uma, S., Saraswathi, M., Siva, S. A., Dhivya Vandana, M. S., Manickavasagam, M., Durai, P., et al. (2008). Diversity and phylogenetic relationships among wild and cultivated bananas (Silk-AAB) revealed by SSR markers. J. Hortic. Sci. Biotechnol. 83, 239–245.
van Asten, P. J. A., Fermont, A. M., and Taulya, G. (2011). Drought is a major yield loss factor for rainfed East African highland banana. Agric. Water Manag. 98, 541–552. doi: 10.1016/j.agwat.2010.10.005
Vanhove, A.-C., Vermaelen, W., Panis, B., Swennen, R., and Carpentier, S. C. (2012). Screening the banana biodiversity for drought tolerance: can an in vitro growth model and proteomics be used as a tool to discover tolerant varieties and understand homeostasis. Front. Plant Sci. 3:176. doi: 10.3389/fpls.2012.00176
Varshney, R. K., Chen, W., Li, Y., Bharti, A. K., Saxena, R. K., Schlueter, J. A., et al. (2012). Draft genome sequence of pigeonpea (Cajanus cajan), an orphan legume crop of resource-poor farmers. Nat. Biotechnol. 30, 83–89. doi: 10.1038/nbt.2022
Vishnevetsky, J., White, T. L., Palmateer, A. J., Flaishman, M., Cohen, Y., Elad, Y., et al. (2011). Improved tolerance toward fungal diseases in transgenic Cavendish banana (Musa spp. AAA group) cv. Grand Nain. Transgenic Res. 20, 61–72. doi: 10.1007/s11248-010-9392-7
Wang, Z., Hobson, N., Galindo, L., Zhu, S., Shi, D., McDill, J., et al. (2012). The genome of flax (Linum usitatissimum) assembled de novo from short shotgun sequence reads. Plant J. 72, 461–473. doi: 10.1111/j.1365-313X.2012.05093.x
WBF: Statistics and data (2012). Banana Statistics and Data. Available at: http://www.fao.org/economic/worldbananaforum/statistics/en/
Wu, W., Yang, Y.-L., He, W.-M., Rouard, M., Li, W.-M., Xu, M., et al. (2016). Whole genome sequencing of a banana wild relative Musa itinerans provides insights into lineage-specific diversification of the Musa genus. Sci. Rep. 6:31586. doi: 10.1038/srep31586
Keywords: Banana/plantain, evolution, structural genome, disease resistance, parthenocarpy, dwarfism, biotic and abiotic stress, comparative genomics
Citation: Dash PK and Rai R (2016) Translating the “Banana Genome” to Delineate Stress Resistance, Dwarfing, Parthenocarpy and Mechanisms of Fruit Ripening. Front. Plant Sci. 7:1543. doi: 10.3389/fpls.2016.01543
Received: 06 August 2016; Accepted: 30 September 2016;
Published: 26 October 2016.
Edited by:Swarup Kumar Parida, National Institute of Plant Genome Research, India
Reviewed by:Ying Wang, South China Institute of Botany (CAS), China
Rajesh MK, ICAR-Central Plantation Crops Research Institute, India
Copyright © 2016 Dash and Rai. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Prasanta K. Dash, firstname.lastname@example.org