Abstract
Cucumber (Cucumis sativus L.) is an important vegetable crop species with great economic value. Shoot architecture determines the visual appearance of plants and has a strong impact on crop management and yield. Unlike most model plant species, cucumber undergoes vegetative growth and reproductive growth simultaneously, in which leaves are produced from the shoot apical meristem and flowers are generated from leaf axils, during the majority of its life, a feature representative of the Cucurbitaceae family. Despite substantial advances achieved in understanding the regulation of plant form in Arabidopsis thaliana, rice, and maize, our understanding of the mechanisms controlling shoot architecture in Cucurbitaceae crop species is still limited. In this review, we focus on recent progress on elucidating the genetic regulatory pathways underlying the determinant/indeterminant growth habit, leaf shape, branch outgrowth, tendril identity, and vine length determination in cucumber. We also discuss the potential of applying biotechnology tools and resources for the generation of ideal plant types with desired architectural features to improve cucumber productivity and cultivation efficiency.
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Introduction
In nature, much of the diversity and beauty observed can be attributed to the tremendous variability in plant architecture. Despite its plasticity to prevailing environmental conditions, shoot architecture has species-specific characteristics, indicating the involvement of genetic regulatory mechanisms. In flowering plants, shoot architecture is largely determined by the organization and activities of meristems, including apical, axillary, and inflorescence meristems1. During the vegetative stage, the shoot apical meristem (SAM), located at the shoot tip, produces leaf primordia from its end in a sequential and modular manner, and vegetative shoots are generated from axillary meristems in leaf axils2,3. Upon transition to the reproductive phase, the SAM turns into an inflorescence meristem (IM) that produces flowers directly or flower-bearing shoots4,5,6. In most plant species, such as Arabidopsis thaliana and rice, the transition from vegetative to reproductive growth is easy to discern. Cucumber (Cucumis sativus L.), an important vegetable crop species in the Cucurbitaceae family, undergoes vegetative growth and reproductive growth simultaneously during the majority of its life, in which leaves are produced from the SAM, while flowers, branches, and tendrils are produced from the leaf axils7,8,9. Therefore, the development of stems, leaves, tendrils, branches, flowers, and fruits determines the shoot architecture of cucumber (Fig. 1A).
Shoot architecture has a strong impact on crop management and yield and thus has been subjected to intense selection during crop domestication and improvement. For example, modern maize has single-culm-bearing ears at the axillary nodes and tassels at the shoot tip (Fig. 1B), whereas its ancestor, teosinte, is highly branched10. Tomato is a model species of sympodial plants that produce compound inflorescences (Fig. 1C); during domestication, its fruit size increased, and its fruit shape became diversified11,12. Similarly, the first Green Revolution resulted in a significant increase in rice yield, mainly due to the rapid adoption of semidwarf cultivars13.
Cucumber, an annual creeping or climbing crop species with unisexual flowers, has a 90~120 day life cycle. Based on nucleotide diversity, cucumber can be divided into four geographic groups: an Indian group, a Xishuangbanna group, a Eurasian group, and an East Asian group7. Compared to the wild ancestor C. sativus var. hardwickii in the Indian group, commercial cucumbers have reduced branches, stronger stems, increased leaf size, and enlarged fruits (Fig. 1A, D). Suitable plant architecture can improve crop yield and reduce labor costs, which is of great importance to feed the increasing population given the limited arable land available. Identifying the key genes and molecular mechanisms controlling shoot architecture is essential for the efficient modification of plant forms with desired architectural traits. In this review, we summarize the recent progress on elucidating the genetic regulatory pathways underlying determinant/indeterminant growth, leaf shape, branch outgrowth, tendril identity, and vine length determination in cucumber. We also describe the potential of applying biotechnology tools and resources to further improve production and cultivation efficiency by breeding ideal shoot architecture into cucumber.
Cucumber has both indeterminate and determinate growth habits
Plants can be divided into two groups based on whether the primary inflorescence axis turns into flowers at the end or not: those that have determinate growth and those that have indeterminate growth. Arabidopsis undergoes indeterminate growth, as its flowers and secondary inflorescence branches are produced from the main stem (Fig. 1E)1, whereas rice undergoes determinate growth, as the primary IM terminates into a spikelet and floral meristems (Fig. 1F)14. In cucumber, vegetative growth and reproductive growth occur simultaneously; thus, it is the SAM, not the IM, which specifies the indeterminate/determinate growth habits15. Most cucumber varieties grown for fresh markets have an indeterminant growth habit, which is advantageous for continuous harvesting when grown in protected environments to obtain high yields, and are adapted for manual harvest16. In contrast, cucumber varieties used in the pickling industry generally undergo determinate growth, which is desirable for mechanical harvesting and high-density planting in open fields17,18.
Indeterminate/determinate growth habit is driven by the balance between IM identify and floral meristem identity, which is regulated by interplay between TERMINAL FLOWER 1 (TFL1), LEAFY (LFY), and APETALA1 (AP1)19,20,21,22. The AP1 and LFY genes are crucial for specifying floral meristem identity in Arabidopsis. AP1 and LFY encode MADS box and plant-specific transcription factors, respectively, which are expressed in the floral meristem. Loss-of-function of AP1 and LFY results in the replacement of initial flowers on inflorescence stems with shoots19,23. In Arabidopsis, LFY and AP1 activate the expression of each other through a positive feedback loop21. TFL1 acts as a key player repressing floral induction and maintaining shoot indeterminacy24,25. Arabidopsis tfl1 mutants display determinate growth, with the conversion of the IM into a terminal flower24. TFL1 encodes a phosphatidyl ethanolamine-binding protein (PEBP) and is expressed in the central region of the IM; TFL1 represses AP1 and LFY expression in the IM22,25,26. In turn, AP1 suppresses TFL1 expression, and LFY promotes the expression of TFL119,21. The mutual regulatory network involving AP1, LFY, and TFL1 shows the complexity underlying floral initiation. SELF-PRUNING (SP), the tomato ortholog of TFL1, has conserved functions in repressing floral induction and maintaining indeterminate growth27. The spontaneous loss-of-function sp mutant exhibits a series of desired characteristics for mechanical harvesting, including determinate growth, reduced plant height, and uniform fruit ripening; therefore, the sp allele was selected and introgressed into modern tomato cultivars27. Similarly, TFL1 homologs in Antirrhinum and rice have conserved functions in inhibiting floral induction and maintaining meristem indeterminacy28,29. Another PEBP, FT, together with TWIN SISTER OF FT (TSF), functions antagonistically with TFL1 in specifying IM identity in Arabidopsis30. SINGLE FLOWER TRUSS (SFT), a FLOWERING LOCUS T (FT) ortholog, and SUPPRESSOR OF SP (SSP), a homolog of Arabidopsis FD, were identified as suppressors of SP to maintain indeterminate growth in tomato11,31,32,33.
In cucumber, mapping for the determinate (de) locus showed that a SNP in CsTFL1 underlies the determinate growth habit16. Knockdown of CsTFL1 by RNAi led to terminal flowers at the shoot apex, confirming the role of CsTFL1 in regulating indeterminate growth in cucumber16. In situ hybridization showed that CsTFL1 transcript signals were present in the subapical regions of the SAM, lateral meristems, and young stems. Biochemical analyses indicated that CsTFL1 competes with CsFT for interaction with the CsNOT2a (negative on TATA-less 2a)-CsFDP (FD PARALOG) complex to suppress floral meristem identity genes in the shoot tip to promote the indeterminate growth of cucumber (Fig. 2)16. CsLFY was cloned in cucumber, and knockdown of CsLFY resulted in disrupted shoot apex development and premature termination of leaf initiation, suggesting that CsLFY has a novel function in regulating shoot meristem maintenance in cucumber. CsLFY directly interacts with CsWUS (WUSCHEL) in the SAM to maintain stem cell identity and thus maintain an indeterminate growth habit15. Therefore, CsTFL1 and CsLFY coordinately regulate the indeterminate growth habit of cucumber by suppressing floral meristem development and promoting stem cell identity in the SAM, respectively (Fig. 2).
In addition, unfavorable environmental conditions can result in the transition from indeterminate growth to determinate growth, referred to as the ‘blunt with blossom’ conditions, during cucumber cultivation. A succession of low-irradiance days, low temperature, and drought are the main factors that give rise to the ‘blunt with blossom’ condition, which is associated with reduced yields of cucumber and decreased cucumber fruit quality17. The genetic mechanisms underlying the above environmental factors leading to ‘blunt with blossom’ remain unidentified in cucumber.
Genetic regulation of leaf morphology in cucumber
Leaves are planar lateral appendages of plants and function as solar panels that capture sunlight, and they are used for carbohydrate and oxygen generation. Leaves also act as the interface for sensing signals of the surrounding environment, including light, temperature, water, insects, and microbes34. Therefore, leaf morphology plays important roles in photosynthesis, planting density, crop yield, and cultivation labor cost. Leaves originate from ends of the SAM and develop into planar structures along three axes: the adaxial–abaxial axis, proximal–distal axis, and mediolateral axis34,35. Considerable advances have occurred in the understanding of the key genes and phytohormones involved in the regulation of leaf initiation, leaf polarity determination, leaf flattening, and intercalary growth of Arabidopsis and tomato34.
Cucumber is a typical dicotyledonous plant species that produces simple leaves; in this case, a single leaf blade is attached to the node by a petiole34,36. A typical leaf of cucumber is palmate, with five primary veins extending from the petiole at the leaf base to the leaf margins to form lobed leaf (Fig. 3A). In recent years, mutants with abnormal leaf morphology have been identified, and several genes have been mapped and characterized (Fig. 3). In the round leaf (rl) mutant, the primary leaf vein branches into secondary or higher-order veins to generate a smooth leaf edge, which results in rounded leaves (Fig. 3B). Fine mapping data showed that the causal gene rl encodes a homolog of the protein kinase PINOID in Arabidopsis (CsPID)36,37,38. PID is involved in the fine-tuning of polar auxin transport through phosphorylation of PIN-FORMED (PIN) proteins in Arabidopsis39. In cucumber, CsPID regulates the distribution of indoleacetic acid (IAA) in leaves by mediating polar auxin transport, biosynthesis, and signaling pathways to drive leaf vein patterning37. A cucumber mango fruit (mf) mutant with a disrupted WOX1-type protein (CsWOX1) displayed lamina developmental defects and abnormal vein patterning. The mf leaves have a butterfly-like shape and substantial growth defects in the mediolateral axis (Fig. 3C)40,41. Based on the genetic analysis of the mf rl double mutant, CsWOX1 functions in leaf vein patterning via CsPID-mediated auxin transport. Moreover, CsWOX1 regulates leaf size by interacting with CIN (CINCINNATA)-TCP (TEOSINTE BRANCHED1/CYCLOIDEA/PCF) proteins41. Two transcription factors, CsIVP (Cucumis sativus Irregular Vasculature Patterning) and CsYAB5 (Cucumis sativus YABBY 5), are highly expressed in vascular tissues to regulate leaf morphology in cucumber42. In CsIVP-RNAi plants, the leaves curl downward, and the bilateral leaf margins overlap due to the enlarged primary veins and increased number of secondary veins (Fig. 3D)42. Similarly, knockdown of CsYAB5 by RNAi led to abnormal leaf morphology with overlapping bilateral leaf margins (Fig. 3E). Biochemical analyses have indicated that CsIVP directly binds the promoter of CsYAB5 to promote its expression to regulate leaf shape in cucumber42. The leaves of two gain-of-function mutants, curly leaf-1 (cul-1) and curly leaf-2 (cul-2), roll upward (Fig. 3F). Mapping data showed that the candidate genes underlying cul-1 and cul-2 are located within a cs-miRNA165/166 target sequence of CsPHB (Cucumis sativus PHABULOSA), a homolog of Arabidopsis PHABULOSA, which belongs to the class III homeodomain-leucine zipper (HD-ZIP III) transcription factor family43. In Arabidopsis, HD-ZIP III transcription factors determine adaxial cell identity in leaf polarity determination, and AtPHB gain-of-function mutants resemble the cur-1 and cur-2 mutants with upward curling leaves, indicating that the function of PHB is conserved in adaxial–abaxial specification during leaf development43,44,45,46. In addition, genes controlling cell proliferation and expansion generally also affect organ size47. The small-leaf phenotype of the little leaf (ll) mutant was due to reduced cell numbers and smaller cell size in cucumber (Fig. 3G), and the candidate gene LL encodes an F-box protein with multiple WD40 repeats, which is a homolog of Arabidopsis SAP (STERILE APETALA)48. In the small and cordate leaf 1 (scl1) mutant, the leaf base is blunt, and the leaf size is reduced due to decreased cell numbers49. Through bulked segregant analysis-based sequencing (BSA-seq), the causal gene of scl1 was identified as Csa7G062760, which encodes a putative nucleoside bisphosphate phosphatase belonging to the polymerase and histidinol-phosphatase (PHP) family within the amidohydrolase superfamily49. CsHAN1 (HANABA TARANU), encoding a GATA3-type transcription factor, also participates in leaf shape development. The leaves of both CsHAN1 overexpression and CsHAN1 knockdown lines are highly lobed, especially those along the first 10 nodes (Fig. 3H)50.
Shoot branching is an important agronomic trait in cucumber
Shoot branching is a fundamental process of plant growth and fitness and is linked to crop yield; thus, shoot branching has been as a selection target during domestication10,12. Compared to the wild ancestor of cucumber with many axillary branches, commercial cucumber cultivars have very few branches due to artificial selection. Cucumber plants grown in protected environments for fresh markets, such as Chinese Long, produces fruits along the main stem, which is adapted for continuous harvesting. Axillary branches need to be manually removed to reduce energy consumption and ensure high yields; however, removal of axillary branches increases labor costs. For cucumber plants grown in open fields for the pickling industry, such as GY14, which produces small fruits, stronger lateral branch growth potential is preferred to improve productivity. Therefore, elucidation of the genetic regulatory mechanism of shoot branching is important for breeding cucumber varieties adapted to different cultivation systems.
The formation of lateral branches is controlled by axillary bud initiation and subsequent bud outgrowth. Lateral Suppressor (LS), a GRAS family transcription factor, regulates the formation of the axillary meristem in tomato. In the ls mutant, lateral meristems do not form during the vegetative stage51. MONOCULM 1 (MOC1) and LATERAL SUPPRESSOR (LAS), the rice and Arabidopsis orthologs of LS, respectively, have conserved functions in bud initiation52,53. The Cucumber Lateral Suppressor (CLS) gene has been cloned, and its transcripts accumulate in leaf axils where axillary meristems initiate54. Ectopic expression of CLS in Arabidopsis fully complemented the reduced number of axillary buds of the las mutant54, indicating the conserved function of CLS in bud initiation in cucumber. Auxin was found to be the primary hormone responsible for apical dominance to repress lateral bud outgrowth55,56. The TEOSINTE BRANCHED 1/CYCLOIDEA/PCF (TCP) family gene known as BRANCHED 1 (BRC1) in eudicots and teosinte BRANCHED 1 (TB1) in monocots was shown to be the key factor repressing shoot branching in different species, including Arabidopsis (AtBRC1), tomato (SlBRC1b), rice (OsTB1), and maize (TB1)57,58,59,60,61. In cucumber, CsBRC1-RNAi lines exhibit increased shoot branching and reduced auxin accumulation in lateral buds62. Biochemical data showed that CsBRC1 inhibits the expression of the auxin efflux carrier PIN-FORMED (CsPIN3) by directly binding to its promoter. Increased expression of CsPIN3 driven by the CsBRC1 promoter resulted in increased numbers of lateral branches and reduced auxin accumulation in the buds62; this study provides a direct link between auxin and CsBRC1 in regulating bud outgrowth in cucumber. During domestication, two insertions of light response elements in the CsBRC1 promoter may have contributed to the increased expression of CsBRC1 in cultivated cucumber in the adaptation to high-density planting and increased productivity (Fig. 4)62.
Cucumber is a climbing plant due to tendrils
Cucurbitaceous crop species can climb via tendrils, which are specialized organs with a filamentous structure arising from leaf axils. Tendrils provide winding support for plants to arrive at higher or advantageous positions for capturing more sunlight or other beneficial resources63,64. Tendrils of cucurbitaceous crop species are modified branches65. Tendrils of cucumber and melon are branchless, whereas those of watermelon and pumpkin are ramate tendrils, with 2–4 branches65,66. Tendrils can twine around other supportive structure during climbing. First, the initially straight tendrils find an attachment point. Then, the touch-sensitive region near the tendril tip senses a thigmotropic signal and begins to climb the perceived structure within seconds or minutes via twining. Finally, tendrils coil by forming two opposing helices with approximately 10 turns on each side of a perversion point to host the plant shoot toward the attachment point65,67,68. Studies have shown that lignified gelatinous fiber ribbons are found on only the ventral side of tendrils, resulting in the ventral side shrinking longitudinally relative to the dorsal side through asymmetric contraction and tendril coiling in cucumber67. For cucumber cultivation in protected environments, the climbing capacity of tendrils gives rise to disorderly growth and inconvenient crop management. Therefore, tendrils need to be manually removed in a timely manner, and the growing direction of the main vines is usually specified via artificial hanging, which greatly increases labor costs. Moreover, the growth and coiling of tendrils utilize a considerable portion of plant biomass. As such, tendrillessness is a desirable agronomic trait for cucumber production and breeding.
Among cucumber germplasm resources, tendrillessness or abnormal tendrils are quite rare; only four genes have been identified as being involved in tendril development in cucumber. In the tendril-less (ten) mutant, tendrils are replaced with branches, and climbing ability of the plant is lost. The causal gene underlying the ten mutant is TENDRIL-LESS (TEN), which encodes a TCP transcription factor expressed specifically in tendrils67. Further study showed that the C-terminus and N-terminus of TEN perform different functions to regulate tendril identity and coiling68. TEN binds to intragenic enhancers (CDCCRCC motifs) of target genes through the C-terminal domain, whereas its N-terminus functions as a noncanonical histone acetyltransferase to preferentially modify the H3 globular domain; thus, the C- and N-terminus coordinately participate in chromatin loosening and host gene activation68. Moreover, ethylene has been found to induce spontaneous tendril coiling, and TEN was shown to be recruited to exons of both ACC OXIDASE 1 (ACO1) and ETHYLENE RESPONSE FACTOR 1 (ERF1) to regulate their transcription. The tendril coiling capacity is substantially altered in aco-1 and aco-2 mutant plants68. Similarly, CLT, the ortholog of TEN in melon, was also identified as a key regulator determining tendril identity69. Another study showed that a histone acetyltransferase encoded by Cucumis sativus GENERAL CONTROL NONDEREPRESSIBLE 5 (CsGCN5) is the candidate gene responsible for the tendril-less mutant B007, in which a nonsynonymous SNP in the first exon of CsGCN5 leads to an amino acid substitution from Asp (D) in the wild-type to Asn (N) in the B007 mutant70, suggesting that histone acetylation status is important for tendril growth and development. In addition to the tendril-less phenotype, B007 mutant plants exhibit pleiotropic phenotypes, including a smooth epidermis, sterile female flowers, and a dwarf stature70. Auxin transport was found to play an essential role in lateral organ morphogenesis. CsPID, whose homolog in Arabidopsis regulates auxin transport via phosphorylation of auxin efflux transporters, was shown to control tendril initiation along the first ~20 nodes of cucumber plants37. The cucumber pid mutant also has decreased numbers of other lateral organs, such as leaves and flowers37.
Vine length is a pivotal factor in cucumber shoot architecture
Grafting cucumber seedlings onto pumpkin (Cucurbita moschata) rootstocks is widely used to improve fruit yield and quality during cucumber cultivation71. Grafting survival rate is strongly influenced by hypocotyl growth of cucumber seedlings. Environmental conditions such as low light, high temperature, and high humidity generally result in excessive growth of the hypocotyl and thus poor seedling quality for grafting and transplanting72. A short hypocotyl 1 (sh1) allele encoding a human SMRCA3-like chromatin remodeling factor is enriched in semiwild Xishuangbanna (C. sativus L. var. xishuangbannesis) and wild (C. sativus L. var. hardwickii) cucumber populations. The sh1 allele allows hypocotyl elongation that is insensitive to UV-B-free light and temperature, which is beneficial for industrialized seedling production of cucumber72. The long hypocotyl (lh) mutant has a saturated shade avoidance response due to the lack of a light-stable PHYB-like phytochrome73. On the other hand, hypocotyl elongation tends to be reduced under high light intensity, which is partly due to gibberellin (GA) deactivation74,75. The levels of two transcripts of Gibberellin 2-beta-dioxygenase (CsGA2ox8) are precisely regulated to control plant height under high-light stress. With increasing light intensity, nonfunctional CsGA2ox8.2 transcripts are generated to buffer against functional CsGA2ox8.1 transcripts to finely tune GA levels75. In addition, a G protein, CsGPA1, was found to positively regulate hypocotyl growth by promoting increased cell size in cucumber overexpression and RNAi-transgenic lines76.
In the adult plant stage, suitable compact plant types are preferred in cucumber production for once-over mechanical harvesting and high-density planting77. Six mutants with dwarf phenotypes have been identified: Cucumber dwarf (Csdw), compact (cp), compact-1 (cp-1), super compact-1 (scp-1), super compact-2 (scp-2), and short internode (si)77,78,79,80,81. The Csdw, cp, cp-1, scp-1, and scp-2 mutants have extremely short internodes and thus little to no practical application value. The length of the internodes of the Csdw mutant is reduced because of decreased cell numbers in the main stem and reduced endogenous GA3 levels, which can be partially rescued by GA3 application. MutMap and kompetitive allele-specific PCR (KASP) genotyping results revealed that CsDW, which encodes a CLAVATA 1-type receptor-like kinase, is the putative candidate gene for the Csdw mutant78. Similarly, fine genetic mapping indicated that the cytokinin oxidase (CKX) and Cullin 1 genes may be potential candidates for the cp and cp-1 mutants, respectively77,82. CsCYP85A1, encoding a brassinosteroid (BR)-C6 oxidase involved in BR biosynthesis, was found to be responsible for the extreme dwarfism of scp-1, and exogenous application of BR could rescue the mutant phenotype83. A spontaneous single-base insertion of DEETIOLATED-2 (CsDET2) led to the supercompact phenotype and systemic BR deficiency of scp-2. CsDET2 encodes a steroid 5-alpha-reductase that acts in the early step in brassinolide synthesis, and exogenous BR treatment could partially rescue the dwarf phenotype of scp-281. CsVFB1, a member of the VIER F-BOX PROTEIN subfamily of the F-Box protein family, was identified to participate in short internode development in the si mutant79. Moreover, both CsIVP-RNAi plants and CsYAB5-RNAi lines displayed a dwarf stature with fasciated vasculature of the stems42.
In addition, flowering time, sex determination, and fruit-related traits have some effect on the shoot architecture of cucumber. Two large deletions (‘short-1’ and ‘short-2’) in upstream sequence of CsFT (Flowering Locus T) were found to be associated with increased CsFT expression and advanced flowering and were distributed mostly in populations at relatively high latitudes, suggesting that CsFT has undergone positive selection during the domestication of acclimatization of cucumber83. Cucumber produces three kinds of flowers: male flowers, female flowers and hermaphroditic flowers. Four genes, F (female), M (andromonoecious), A (androecious), and Gy (gynoecious), control cucumber sex determination by regulating ethylene biosynthesis84. For fruit-related traits such as fruit shape, fruit color, fruit spine, the presence of fruit warts, and fruit wax, numerous studies have been performed, and specific reviews on cucumber should be consulted for additional details85.
Perspectives
In this work, we summarized 25 genes identified as being involved in shoot architecture traits, including determinate growth habit (2), leaf morphology (8), lateral branching (3), tendril formation (4), vine length (10), and flowering (1); among them, CsPID, CsIVP, and CsYAB5 are involved in two developmental processes (Table 1). Most of these have been cloned from natural germplasm resources, obtained from spontaneous mutations, or cloned from EMS-induced mutagenesis populations, and some of them were identified by transgenic analyses (Table 1). Shoot architecture is a holistic and systematic phenotype, and mutations in one gene often cause changes in multiple organs, which is undesirable for fine-control strategies of modern breeding. For example, despite tendrillessness being a desirable feature in the td-1 mutant, severe dwarfism and sterile flowers are deleterious to yield and thus are associated with decreased value in terms of cucumber breeding70. In another tendril-less mutant (ten), tendrils are replaced only by short branches, and other developmental processes are unaffected66. Hence, the ten alleles serve as an important genetic resource for designing ideal cucumber architecture. In addition, some well-known genes have potential use in cucumber breeding. For example, the suitable compact shoots of si are preferred for once-over mechanical harvesting and high-density planting79; sh1 hypocotyl elongation that is insensitive to UV-B-free light and temperature is desired for industrialized seedling production72; CsBRC1, a suppressor of branch outgrowth, is useful for cucumber varieties for fresh fruit production62; and the early flowering caused by ‘short-1’ and ‘short-2’ in the upstream region of CsFT is advantageous for early marketing and extended harvest83.
Although a large number of plant architecture-related genes have been reported to benefit from rapid advances in techniques in the last five years, some important architectural traits have not yet been investigated in cucumber. For example, leaf angle and lateral branch angle, which greatly affect planting density and crop yield per unit area, await further studies in cucumber. A relatively small leaf angle can improve the accumulation of photosynthetic products by decreasing the amount of mutual shading to capture light for photosynthesis under dense planting, and several genes, such as Related to ABI3/VP1-Like 1 (ZmRAVL1) and BRASSINOSTEROID-RESPONSIVE LEAF ANGLE REGULATOR 1 (OsBLR1), have been identified to play essential roles in this trait in both maize and rice86,87. The leaf angle of cucumber plants is even more complex than that of maize and rice, and it is coordinately determined by the angles among the leaf blade, petiole, and stem. Similarly, lateral branch (tiller) angle was shown to directly affect planting density and crop yields, and genes such as PROSTRATE GROWTH 1 (PROG1) and LAZY1 (LA1) are the key players of this trait in cereal crop species88,89. Nonetheless, functions of the above homologous genes in cucumber remain elusive and deserve further exploration.
Cucumber is planted all over the world, with several variations in cultivation methods, including open field or greenhouse production, manual harvesting or mechanical harvesting, and productions of fruits for fresh markets or processed pickling. Therefore, the requirements for ideal shoot architecture are different depending on the cultivation method. For cucumber plants cultivated in protected environments for fresh markets, architectural traits such as an indeterminate growth habit, no branching, no tendrils, strong main stems, and small leaf angles are desired. For cucumber plants grown in the open field for processing, moderate determinate habits and branching, compact shoots, and no tendril are advantageous traits composing the ideal shoot architecture.
Future work will not only continue to explore the genes and regulatory mechanisms underlying architectural traits but also identify and integrate appropriate gene resources for fine breeding. An increasing number of bioinformatics and transgene-free techniques based on CRISPR provide the possibility to achieve this goal. With cucumber serving as the model plant species of cucurbits, the genome sequence information of four varieties has been released and updated: the North China spiny-type Chinese Long, the North American pickling cucumber Gy14, the wild cucumber Hardwickii (http://cucurbitgenomics.org/), and the North European B10 line (GenBank No. LKUO00000000)7,90,91,92. In addition, deep resequencing of 115 cucumber lines provides a genetic basis of cucumber domestication and diversity7. Such progress has facilitated the identification of suitable genes to generate ideal shoot architecture in cucumber. Furthermore, the development of sequencing tools such as RNA-seq, ChIP-seq, and methylation-seq plays a vital role in the study of molecular modulation mechanisms93. The CRISPR-Cas9 system, currently the premier genome-editing technique, has been shown to have great application value in the breeding of several crop species, including rice, maize, and tomato94,95,96. CRISPR-Cas9 can be used to edit coding DNA sequences, cis-regulatory regions, or other sites influencing gene expression to integrate multiple favorable traits and greatly shorten the breeding process97. Moreover, transgene-free plants can be obtained via CRISPR-Cas9 through self-crossing T0 transgenic lines, which greatly increases the possibility of gene-edited vegetables entering the market in the future98. De novo domestication has been proposed in tomato96, and CRISPR-Cas9 has been used successfully in cucumber99, which provides the possibility for rapidly breeding cucumber varieties with an ‘ideal plant type’ for different cultivation methods in the future.
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Acknowledgements
We thank Dr. Yuhong Li, Dr. Luming Yang, Dr. Xueyong Yang, and Dr. Chengzhen Sun for providing original images shown in Figs. 3 and 4. This work is supported by grants from the National Natural Science Foundation of China (32025033 and 31930097) and the National Key Research and Development Program (2018YFD1000800).
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X.Z. and X.L. conducted the literature review and wrote the manuscript. J.C. provided comments and modified the manuscript. All the authors have reviewed and approved the final submission.
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Liu, X., Chen, J. & Zhang, X. Genetic regulation of shoot architecture in cucumber. Hortic Res 8, 143 (2021). https://doi.org/10.1038/s41438-021-00577-0
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DOI: https://doi.org/10.1038/s41438-021-00577-0
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