Parthenocarpic tomato mutants, iaa9-3 and iaa9-5, show plant adaptability and fruiting ability under heat-stress conditions

Fruit set is one of the main problems that arise in tomato plants under heat-stress conditions, which disrupt pollen development, resulting in decreased pollen fertility. Parthenocarpic tomatoes can be used to increase plant productivity during failure of the fertilisation process under heat-stress conditions. The aim of this study were to identify the plant adaptability and fruiting capability of ?iaa9-3 and iaa9-5 tomato mutants under heat-stress conditions. The iaa9-3 and iaa9-5 and wild-type Micro-Tom (WT-MT) plants were cultivated under two temperature conditions: normal and heat-stress conditions during plant growth. The results showed that under the heat-stress condition, iaa9-3 and iaa9-5 showed delayed flowering time, increased number of flowers, and increased fruit set and produced normal-sized fruit. However, WT-MT cannot produce fruits under heat stress. The mutants can grow under heat-stress conditions, as indicated by the lower electrolyte leakage and H2O2 concentration and higher antioxidant activities compared with WT-MT under heat-stress conditions. These results suggest that iaa9-3 and iaa9-5 can be valuable genetic resources for the development of tomatoes in high-temperature environmental conditions.


Introduction
Tomato (Solanum lycopersicum) is an essential Solanaceae horticultural commodity in the world (Anas et al., 2022). Tomatoes are generally used as a source of nutrients and antioxidants, such as vitamins A, C and B, calcium, potassium, magnesium, sodium, iron, phenolic antioxidants, flavonoids, lycopene and ascorbic acid (Oboulbiga et al., 2017;Mubarok et al., 2019a;Mubarok et al., 2023). Tomato production is affected by several factors, such as genetics, nutrition and cultivation methods and environmental factors, including temperature.
Temperature is a very important environmental factor for the growth and development of tomato plants. Heat stress is an external factor that often becomes an obstacle to tomato cultivation. In general, heat stress occurs when temperatures are 10°C-15°C higher than optimum cultivation temperatures; for tomato growth, the optimum temperature is 26°C and heat stress starts to occur when air temperature exceeds 32°C (Sato et al., 2000;Pham et al., 2020). Heat stress is one of the principal abiotic stresses in tropical countries that limit plant growth and development, affecting production. Failure in pollen development and increased pollen sterility are the main problems in tomato production under heat stress, resulting in a low fruit set (Ezura et al., 2019). The Intergovernmental Panel on Climatic Change reported that in 2014, each country's average world temperature increased by 0.3°C due to global warming and is predicted to increase by 3°C from the usual temperature in 2100. Increased temperature due to global warming has become a severe problem in the agricultural sector. Thus, new tomato cultivars suitable for high-temperature conditions must be developed.
Environmental temperatures above 35°C in tomato cultivation damage plant growth and development, including seed germination, vegetative and reproductive growth, fruit setting and photosynthetic activity (Ariizumi et al., 2013;Rahmat et al., 2023). The severity of heat stress depends on the duration and time of heat-stress exposure. Ariizumi et al. (2013) reported that ambient temperature 4 degrees above optimal temperature will increase tomato flower abortion. Flower abortion occurred due to the failure of pollination and fertilisation, and flower abortion reduces fruit set initiation. Generation of parthenocarpic tomatoes can be an alternative option to resolving the problem in fruit set initiation under heat-stress conditions, which causes reduced fruit formation due to pollen sterility.
Auxin (AUX) triggers fruit set in tomatoes by activating cell division in the pericarp (i.e. phase II); therefore, induction of parthenocarpic fruits can be artificially attained by the application of exogenous AUX in tomato flowers or flower buds (Ariizumi et al., 2013). By mutation methods, two parthenocarpic tomatoes, namely, iaa9-3 and iaa9-5, have been generated from the Micro-Tom (MT) library. Compared with the wild type, iaa9-3 and iaa9-5 produced higher rates of parthenocarpic fruit production, with values reaching up to 70.0% ± 4.7% and 63.3% ± 5.4%, respectively, from an emasculated flower. Meanwhile, in the wild-type MT (WT-MT), almost none of the emasculated WT-MT flowers exhibited fruit formation (Saito et al., 2011). iaa9-3 and iaa9-5 have a mutation in IAA9, which is a member of the AUX/indole-3-acetic acid (IAA) gene family and acts as a transcriptional repressor of the signalling pathway of the plant hormone AUX (Guilfoyle and Hagen, 2007). Different locations of mutations occur in iaa9-3 and iaa9-5. In iaa9-3, a single-DNA substitution causing a T to A substitution was found at the 237th nucleotide, whereas in iaa9-5, a 32 bp deletion was located at the 133rd nucleotide position. These mutations by DNA substitution or deletion in these mutants result in the modification of the functional activity of IAA9, which triggers fruit development prior to pollination or parthenocarpy (Saito et al., 2011).
Parthenocarpic mutants, such as iaa9-3 and iaa9-5, can produce fruits under heat-stress conditions and help maintain stable tomato production in the future. Those two mutants also can growth under drought stress (Suminar et al., 2022). However, the ability of such mutants for plant growth and development, especially in the fruit set under heat-stress conditions, should be carefully evaluated. In this study, we evaluated the fruit set ability of two mutants under tropical heat-stress conditions.

Plant materials and cultivation condition
The iaa9-3 (TOMPJE2811) and iaa9-5 (TOMJPG0114-1) mutants were isolated and characterised from a mutant population based on MT cultivars (Saito et al., 2011). These mutants and WT-MT as control were cultivated in the greenhouse of the experimental field of the Laboratory of Horticulture, Faculty of Agriculture, Universitas Padjadjaran, with four biological replications; each replication consisted of six individual plants for vegetative analysis. The iaa9-3 and iaa9-5 mutants and WT-MT seeds were sown in plug trays, in accordance with the methods described by Rahmat et al. (2023). After the seedling produced 4-5 leaves, they were transplanted into a 12 cmdiameter pot that was filled with a mixture of soil and commercial coir coco peat (1:1/v:v) and cultivated in two greenhouse conditions, i.e. heat-stress (40°C/45°C) and control (30°C/35°C ) conditions. The heat stress condition was treated for the whole lifespan of the plant, starting from transplanting until the fruit harvest. During the cultivation periods, the plants were fertigated with a commercial nutrient solution with an electrical conductivity (EC) level of 2.0-2.5 dS m −1 .

Agronomic-related yield evaluation of iaa9-3 and iaa9-5 mutants
The agronomic features related to plant growth and yield were evaluated. For plant growth, plant canopy diameter that measured as the method described by Iizuka et al. (2017) and the number of shoots were evaluated at 8 weeks after sowing. For plant yield, several characteristics were evaluated; these characteristics included flowering time that was the number of days from sowing until 1 st flowering from each plant (Mubarok et al., 2019c), the number flowers per plant, the number of fruits per plant, the rate of fruit set, fruit weight, length and diameter and the number of seeds. The fruit weight per plant was calculated by dividing the total fruit weight by the total fruit number. The total number of flowers and fruits and the rate of fruit set were counted similarly to those in the study by Pham et al. (2020) at 115 days after sowing. Meanwhile, the rate of fruit set was calculated by dividing the total number of fruits by the total number of flowers. The fruit weight, length and diameter and the number of seeds per fruit were obtained from five individual fruits of each plant.

Pollen viability analysis
Pollen viability testing was carried out using 2,3,5-triphenyl tetrazolium chloride (TTC) in accordance with the method used by Ezura et al. (2019). TTC staining is an indicator of cellular survival based on the mitochondrial reduction reaction, where the viable pollen will turn red, and the non-viable pollen will be colourless. Pollens were obtained from five individual flowers, soaked in 1% TTC +50% sucrose and shaken for dispersal in the solution. Afterwards, the TTC solution containing the pollens was left in a dark room at 38°C for 3 h for pollen colouration. Then, 2 μg supernatant was collected and placed in the cell counter. The pollens were then observed under a microscope. The criterion for viable pollens was the absorption of red colour from the TTC solution per 1 mm 2 cell counter.

H 2 O 2 concentration analysis
H 2 O 2 concentration was measured following the method used by the Association of Official Analytical Chemists (AOAC) with modifications (Association of Official Analytical Chemists, 1990). A total of 5 g leaf sample was mixed with 5 mL Aqua Bidest using mortar and pestle in an ice bath. Then, 5 mL ground leaf sample mixture was combined with 25 mL sulfuric acid. The mixture was titrated with 0.1 N potassium permanganate. Each 1 mL of potassium permanganate used in titration corresponded to 1.07 mg H 2 O 2 . Titration was stopped when the sample mixture changed colour. H 2 O 2 was calculated using the following formula:

Antioxidant activity analysis
Antioxidant activity was analysed following the method used by Sami and Rahimah (2016). A total of 3 g leaf sample was macerated using methanol (99.8%) for 24 h. After 24 h, the mixture was filtrated using filter paper, and the filtrate was thickened utilising a rotary evaporator. The leaf extract solution (1000 ppm) was created by combining 50 mg thickened leaf extract with 50 mL methanol (99.8%). Next, 0.5 mL 0.4 mM 2,2-diphenyl-2-picrylhydrazyl (DPPH) solution was added to a test tube containing 500 μL leaf extract solution (1000 ppm). The test tubes containing the mixture were then incubated in the dark for 30 min at room temperature. After incubation, each sample absorbance was observed using a spectrophotometer (Orion ™ AquaMate 8000, Thermo Fisher Scientific, UK) at 516 nm (Mubarok et al., 2019b). A blank solution containing methanol and DPPH only was also prepared. Sample antioxidant activity was measured using the following equation: Blank absorbance − Sample absorbance Blank absorbance Â 100 %

Statistical data analysis
The normalities of data distributions were tested using the Kolmogorov-Smirnov test. For statistical data analysis, data were subjected to a two-factor analysis of variance followed by Duncan's multiple range test at p< 0.05 for comparisons among the investigated data. The data are represented as the mean values ± standard error (SE) of four replicates. All statistical analyses were performed using SPSS 20.0 statistical software.

iaa9-3 and iaa9-5 exhibited a reduction in vegetative plant growth compared with WT-MT
The response of plant vegetative growth can be observed from the plant appearance, which was characterised by the plant canopy diameter and the number of shoots. Based on statistical data analysis, the plant canopy diameter of WT-MT, iaa9-3 and iaa9-5 mutants were significantly different in either normal temperature or heat-stress conditions (Figures 1A-C, respectively). Hightemperature/heat-stress condition greatly influenced the size of the plant canopy diameter. Under heat-stress conditions, the plant canopy diameter decreased significantly in all plant genotypes compared with plants under normal conditions. The highest reduction in the plant canopy diameter was observed in WT-MT, and it decreased by approximately 41.3% compared with that under normal condition. The plant canopy diameters of iaa9-3 and iaa9-5 decreased by 40.6% and 36.7%, respectively ( Figures 1A, C).
At both temperatures tested, the plant canopy diameter of WT-MT was larger than those of iaa9-3 and iaa9-5. As shown in Figure 1A, the plant canopy diameter of WT-MT under normal conditions showed the highest diameter, but it was not significantly different from that of iaa9-3. Meanwhile, iaa9-5 had significantly lower values compared with WT-MT and iaa9-3 ( Figure 1A). The large plant canopy diameter of WT-MT can also be monitored under heat-stress condition, where the plant canopy diameters of iaa9-3 and iaa9-5 were significantly lower than that of WT-MT ( Figure 1A).
Many lateral shoots caused the large plant canopy diameter of WT-MT. Statistical data analysis showed a significant difference in the number of lateral shoots between WT-MT and iaa9-3 and iaa9-5 under normal and heat-stress conditions. The heat-stress condition significantly inhibited the growth of new lateral shoots in all investigated plant genotypes, which resulted in a low number of lateral shoots under heat-stress conditions. However, no further reduction in lateral shoots was observed in iaa9-3 under heat stress ( Figure 2B). The decrease in the number of lateral shoots under heat-stress condition was 23.50%, 17.35% and 38.36% lower compared with those under normal conditions for WT-MT, iaa9-3 and iaa9-5, respectively. Under normal and heat-stress conditions, the mutation in the IAA9 gene significantly reduced the number of lateral shoots in iaa9-3 and iaa9-5. In iaa9-3, the number of lateral shoots was 5.75 and 4.25 fewer compared with that in WT-MT under normal and heat-stress conditions, respectively. Iaa9-5 showed 5.25 and 4.45 fewer lateral shoots compared with WT-MT under normal and heat-stress conditions, respectively (Figures 2A-C).

Mutant genotypes iaa9-3 and iaa9-5 experienced delayed flowering under the heat-stress condition
Flowering is strongly influenced by internal and external factors. The time of flowering is one of the several indicators of a plant entering the generative phase. The results showed that the flowering time of the three observed tomato genotypes, namely, iaa9-3, iaa9-5 and WT-MT, differed depending on environmental conditions. Under the normal-temperature condition, the mutation in iaa9-3 and iaa9-5 significantly accelerated flowering time by 3 and 6.7 days earlier than WT-MT, respectively ( Figure 3). This result was different from that observed under heat-stress condition. Accelerated flowering time was observed in WT-MT, but iaa9-3 and iaa9-5 experienced a delay in flowering time. The mutants behaved as WT under normal condition when subjected to heat stress.

The number of flowers increased under heat stress condition
The flower is an important generative organ for fruit formation. Statistical analysis showed a significant difference in the number of flowers among the tested genotypes under normal and heat-stress conditions. WT-MT had 94.5 and 122.5 more flowers in normal and heat-stress conditions, respectively. Meanwhile, iaa9-3 and iaa9-5 had 68.7 and 74.1 flowers under normal conditions and 91.6 and 84.8 flowers under heat-stress conditions, respectively. Raising the ambient temperature to 45°C during the growth period significantly increased the number of flowers on all tested plants. The number of flowers of WT-MT, iaa9-3 and iaa9-5 increased by 29.63%, 33.33% and 14.43%, respectively; under heat stress compared with those under normal condition (Figure 3).

Pollen viability decreased under heatstress conditions
In the microscopic analysis of pollen viability, three groups, namely, viable, semi-viable and non-viable pollens were determined based on pollen viability level. Based on statistical data analysis, under normal conditions, the percentage of viable, semi-viable and non-viable pollens in the three genotypes of investigated plants did not show any significant difference. Among the three levels of the proportion of pollens, the group of viable pollens had the highest percentage compared with the semi-viable and non-viable pollen groups.
This study proved that the decrease in pollen viability occurred under heat-stress conditions. Raising the temperature up to 45°C significantly reduced the level of pollen viability in all investigated genotypes. The decrease in the percentage of viable pollen under heat-stress conditions occurred in WT-MT, where the percentage of viable pollen decreased by almost 87.15% compared with that under normal condition. Mutations in the IAA9 gene can prevent pollen damage under heat-stress condition, as indicated by the percentages of viable pollen in iaa9-3 and iaa9-5, which reached 32.62% and 33.42%, respectively. The percentages decreased by 49.73% and 47.51%, respectively, compared with those under normal condition. The decrease in the number of viable pollens under heat-stress condition was caused by the increase in pollen sterility, which resulted in a very high number of non-viable pollens in WT-MT (67.57%) due to high temperature, and the decreases in iaa9-3 and iaa9-5 reached 32.97% and 32.56%, respectively ( Figure 4B).

iaa9-3 and iaa9-5 can produce fruit under heat stress
The fruit set is the percentage ratio of the number of fruits and the number of flowers in the same individual plant. Statistical analysis showed that the fruit set in iaa9-3 and iaa9-5 was significantly higher than that in WT-MT under normal and heatstress conditions ( Figures 5A, B, respectively). Plant capacity to produce fruit also differed between normal and heat-stress conditions, irrespective of genotypes. Under normal conditions, the fruit sets of iaa9-3 and iaa9-5 were 81.24% and 64.89% or 21.57% and 5.22% higher than that of WT-MT, respectively. The percentage of fruit set from all tested plants decreased dramatically under the heat-stress condition at 45°C ( Figure 5C). Under the heat-stress condition, WT-MT was unable to produce fruits, whereas iaa9-3 and iaa9-5 did. Thus, mutations in the IAA9 gene can increase the percentage of fruit set in iaa9-3 and iaa9-5 compared with WT-MT under heat-stress conditions. Although both mutants can produce fruit sets under heat-stress conditions, the fruit set was lower compared with that in normal conditions. The fruit sets of iaa9-3 and iaa9-5 under heat-stress conditions were 34.98% and 32.84% or 46.26% and 32.05% lower than those under normal conditions, respectively ( Figure 5C).
3.6 iaa9-3 and iaa9-5 can produce normal fruit size under heat stress The number of fruits per plant, individual fruit weight and fruit diameter can be used as yield and yield quality variables of tomato fruit. Under the normal-temperature condition, all tested genotypes produced fruits. WT-MT plant produced the highest fruit number and significantly differed from the iaa9-3 and iaa9-5. Under normal conditions, the number of fruits for WT-MT, iaa9-3 and iaa9-5 were 53.3, 47.8 and 46.8 fruits per plant, respectively. The heat condition affected the fruit yield of all investigated genotypes, with the lowest value detected in WT-MT. WT-MT had a small fruit size with no seed inside. However, iaa9-3 and iaa9-5 can still produce fruits under heat-stress condition, with the value being reduced compared with that under normal condition. Under heat condition,  Flowering time and flower number per plant of WT-MT, iaa9-3 and iaa9-5 under two temperature conditions, i.e., normal temperature and heat stress condition. The average value ± standard error (SE) (n = 4) followed by the same lowercase letters is not significantly different based on Duncan's Multiple Range Test at 5%. the reduction of fruit number varied compared to that in normal condition, i.e. 97.75%, 42.34% and 48.68% for WT-MT, iaa9-3 and iaa9-5, respectively ( Figure 6A).
Fruit size can be indicated by individual fruit weight, length and diameter. Under normal condition, iaa9-3 and iaa9-5 had a smaller fruit size, indicated by shorter fruit length and diameter and smaller fruit weight, compared with WT-MT. However, the fruit length of iaa9-3 was comparable to that of WT-MT. Under the heat-stress condition, iaa9-3 and iaa9-5 resulted in a longer fruit length and higher fruit diameter compared with WT-MT ( Figures 6B-D).
Although iaa9-3 and iaa9-5 had a few fruit numbers under heatstress condition, both mutants had a larger fruit size compared with that under normal condition. From the data obtained, Figure 6 indicate a positive relationship between fruit number and fruit size, where more fruits were produced ( Figure 6A), which resulted in smaller fruit sizes and weights ( Figures 6B-D). Statistical data analysis showed that the individual fruit weights of iaa9-3 and iaa9-5 were significantly smaller than those of WT-MT under normal condition. However, both mutants had significantly higher fruit weight than WT-MT under heat-stress condition ( Figure 6B).
In all investigated plants, the number of seeds was highly affected by genetic factors and environmental conditions. Mutation in the IAA9 gene had a significant effect on the number of seeds. Under normal conditions, iaa9-3 and iaa9-5 had lower numbers of seeds compared with WT-MT, with reductions of up to 55.82% and 37.73%, respectively ( Figure 6E). Heat stress significantly reduced the number of seeds in all investigated plants. Under the heat-stress condition, although iaa9-3 and iaa9-5 resulted in a larger fruit size compared with that under normal conditions, both mutants and WT-MT cannot produce seeds because of the heat-stress condition ( Figure 6E).

Mutation in the IAA9 gene significantly reduced H 2 O 2 content but showed increased antioxidant activity
H 2 O 2 content was analysed to predict the accumulation of reactive oxygen species (ROS) within their leaves as an effect of IAA9 mutation under two different environmental conditions. Statistical data analysis showed that H 2 O 2 content differed under various plant genotypes and environmental conditions. Under normal conditions, the H 2 O 2 content was lower than that under heat-stress conditions in all plant genotypes. Mutation in the IAA9 gene significantly reduced H 2 O 2 content in iaa9-3 and iaa9-5 compared with WT-MT, with values of 0.44 and 1.90 μmol/g FW, respectively, which is lower than that of WT-MT The proportion of pollen of WT-MT, iaa9-3 and iaa9-5 under two temperature conditions, i.e., (A) normal temperature and (B) heat stress condition. The average value ± standard error (SE) (n = 4) followed by the same lowercase letters is not significantly different based on Duncan's Multiple Range Test at 5%. Fruit set of WT-MT, iaa9-3 and iaa9-5 under two temperature conditions, i.e., (A) normal temperature and (B) heat stress condition. (C) The average value of fruit set under normal temperature and heat stress conditions. The average value ± standard error (SE) (n = 4) followed by the same lowercase letters is not significantly different based on Duncan's Multiple Range Test at 5%.
( Figure 7A). Environmental conditions significantly affected the content of H 2 O 2 in plants. The rise in temperature resulted in the increased H 2 O 2 content in all investigated plants, but iaa9-3 and iaa9-5 showed a lower H 2 O 2 content compared with WT-MT. WT-MT had a significantly higher H 2 O 2 content than iaa9-3 and iaa9-5, but it was comparable between iaa9-3 and iaa9-5. The increase in H 2 O 2 content under heat-stress conditions varied among genotypes, with values of 1.22, 0.56 and 1.82 μmol/g FW for WT-MT, iaa9-3 and iaa9-5, respectively. These values were higher than those under normal conditions ( Figure 7A).
Antioxidant activity values directly influence ROS accumulation in plants. Antioxidant activity varied among genotypes under normal or heat-stress conditions. The statistical data analysis of antioxidant activity revealed a significant difference in antioxidant activity among genotypes under normal or heat-stress conditions (Figure 7). Under normal conditions, iaa9-5 showed the highest leaf antioxidant activity, followed by iaa9-3 whose value was significantly higher than that of WT-MT. A significant increase in antioxidant activity was detected when the plant was exposed to high temperatures or heat stress. Under heat-stress conditions, similar findings with normal conditions were observed. iaa9-3 had the highest antioxidant activity, followed by iaa9-3 and WT-MT, with increased antioxidant activities of 248.90%, 152.22% and 171.92% compared to the under normal conditions for WT-MT, iaa9-3 and iaa9-5, respectively ( Figure 7C).

Discussion
Tomato productivity is greatly affected by heat stress. Heat stress-induced male gametophyte abortion leads to fruit set reduction (Alsamir et al., 2021). The reduction of fruit set showed a consequence in reducing plant yield, which is a major problem in tomato production. The use of parthenocarpic tomatoes is an interesting approach to improving tomato production in heatexposed locations, especially in the tropics. iaa9-3 and iaa9-5 resulted in a parthenocarpic tomato without any fertilisation process. Therefore, these tomatoes can be developed with a hightemperature characteristic for growing in the tropics. However, these mutants should be further evaluated to gain more information regarding their growth and development performances under heatstress condition.
The diameter of the plant canopy is one of the plant growth variables that can show the response of plants to environmental conditions. Heat stress greatly affects plant growth, which can be characterised by a decline in vegetative growth, resulting in small plant size, such as the small canopy diameter observed compared with that under normal condition (Figure 1). Mutations in iaa9-3 and iaa9-5 resulted in smaller plant canopy diameters compared with that of WT-MT under normal or heat-stress conditions. The small number of lateral shoots produced caused the small diameter in the mutants. By contrast, the WT-MT compound leaf shape formed a longer leaf stalk and wider plant shape, resulting in a wider plant diameter (Figure 1). According to Valladares et al. (2007), the shape of a plant canopy is determined by the shape of leaves, lateral shoots and branching patterns. A high number of branching results in a wide plant canopy development.
The loss function of IAA9 caused changes in the growth pattern of the shoot, which inhibited the growth of the lateral shoot. Inhibition of lateral shoot growth decreased the number of lateral shoots of iaa9-3 and iaa9-5 (Figure 2). Tezuka et al. (2011) stated that a high AUX level can inhibit lateral shoot regeneration in tomato plants. Wang et al. (2005) reported a contradictive study that the AS-IAA9 plant showed decreased apical dominance. Heat stress also reduces plant growth by lowering plant stomatal conductance (Camejo et al., 2005). A low stomatal conductance reduces CO 2 fixation while increasing leaf temperature, resulting in reduced photosynthesis and more oxidative damage in leaf tissue (Hemantaranjan, 2014).
The iaa9-3 and iaa9-5 experienced lateral shoot growth reduction, which led to a decline in the number of flowers compared with that in WT-MT under normal and heat-stress conditions (Figures 2 and 3). Under normal conditions, the flowering times of iaa9-3 and iaa9-5 were shorter than that of WT-MT. Possibly, mutations in iaa9-3 and iaa9-5 sped up flowering. According to Cheng and Zhao (2007) AUX plays an important role in the initiation of flower primordia. The shoot apical meristem turns into a flowering meristem that can initiate the floral meristem, in which AUX plays a role in regulating the proliferation of flower meristematic cells (Merelo et al., 2022). The role of AUX in primordial formation was evidenced by the increase in AUX concentration at the primordial tip of the flower (Vanneste and Friml, 2009). Accelerated flowering in WT-MT under heat stress was caused by the shortened plant life cycle (Solankey et al., 2015), but mutation in the IAA9 gene can slow down the flowering process.
The highest number of lateral shoots was identified in WT-MT, resulting in a higher number of flowers on WT-MT either in normal or heat-stress conditions. Apical meristem can transform either into vegetative organs, such as leaves or reproductive organs, such as flowers (Ohta, 2018). Lateral shoots at certain points on determinate tomatoes can form bunches as a growth site of flowers and fruit (Park et al., 2016). AUX is directly involved in the formation of axillary buds. With the mutation of the IAA9 gene, the number of lateral shoots in iaa9-3 and iaa9-5 mutants and the number of flowers produced decreased. Heat stress treatment up to 45°C caused a significant increase in the number of flowers on all tested genotypes than those under normal conditions, with a higher number of flowers observed on WT-MT than on iaa9-3 and iaa9-5 ( Figure 3). The increased number of flowers under heat stress was in accordance with the statement of Park et al. (2016), who stated that high temperatures can induce flower growth as a plant adaptation to maintain its generation.
Pollen viability is a crucial factor in determining the success of fruit formation. The results of this study showed that mutations in iaa9-3 and iaa9-5 can increase the number of viable and semi-viable pollens and reduce the number of non-viable pollens under normal temperature or heat stress. According to Aloni et al. (2006) endogenous AUX plays an important role in the growth of the pollen tube that will penetrate the ovule, as evidenced by the increased concentration of IAA in the pistil after pollination. Sakata et al. (2010) stated that the application of AUX can increase the anther length, prevent pollen abortion and improve the viability of mature pollens. AUX can block transcriptional changes, which result in normal pollen production and prevent pollen sterility under heat stress (Higashitani, 2013). According to Pan et al. (2019) IAA can increase the fresh weight of stamens and pistils in tomato flowers when exposed to heat stress. At temperatures of 40°C-45°C, WT-MT had the lowest number of viable and semi-viable pollen and the highest number of non-viable pollens compared with both mutants. Thus, WT-MT had the highest potential for male sterility, which can affect fruit formation (Figure 4).
Tomato reproduction is extremely sensitive to heat stress. High temperatures can cause abortion of the male gametophyte, which leads to a reduction in fruit set. The increased fruit set in iaa9-3 and iaa9-5 under normal and heat-stress conditions was caused by the mutation in the IAA9 gene. AUX synthesis can increase fruit set in tomato plants by preventing flowering and fruit fall (Batlang, 2008;Pramanik and P. Mohapatra, 2017). Mutations in the IAA9 gene caused a reduction in the accumulation of mRNA, which triggered tomato fruit development before pollination, resulting in parthenocarpic fruit formation (Wang et al., 2005). AUX accumulation in the ovary vasculature and the micropylar pole of the ovule embryo sac for six days before anthesis was distributed to the ovule for two days before anthesis and finally localised to the interior and surface of the ovarian wall during anthesis (Pattison and Catala, 2012). Under the heat-stress condition, WT-MT showed no ability to produce fruit ( Figure 5) although it produced a large number of flowers ( Figure 4). Solankey et al. (2015) stated that the rise in temperature affected the development of gametes and embryos and inhibited the ability of pollinated flowers to develop into seeds. Saito et al. (2011) stated that iaa9-3 and iaa9-5 are parthenocarpic tomato mutants with the ability to form fruit without fertilisation. Therefore, these tomatoes are very good candidates for tomato development in areas with the hightemperature condition that generally limits tomato productivity.
Both iaa9-3 and iaa9-5 can produce fruit without fertilisation due to a mutation in the IAA9 gene under normal or heat-stress conditions. Heat stress caused a decrease in plant growth and development, which affected the yield, especially the number of fruits. Kumar et al. (2022) stated that exposure of plants to extreme temperatures limits their ability to produce fruit due to disruption of the pollination process. At normal temperatures, the number of fruits in both mutants was less than that in WT-MT. This finding was caused by the small number of flowers that formed in the mutants compared with WT-MT, which resulted in the formation of fewer fruits. Under the heatstress condition, WT-MT did not produce fruits due to the failure of the fertilisation process as the effect of lowered pollen viability (Figure 4). Extremely high temperatures during the reproductive stage affect pollen viability, fertilisation and grain or fruit formation (Hatfield and Prueger, 2015). Nonviable pollens cannot pollinate flowers, causing failure in the fruit set (Sato et al., 2000). Meanwhile, iaa9-3 and iaa9-5 can produce fruits under heat stress. This result was due to the nature of the two tomatoes, which were parthenocarpic tomatoes, to form fruit without fertilisation (Ariizumi et al., 2013). The results showed that iaa9-5 had the lowest fruit weight at normal temperatures. IAA9 gene mutation in iaa9-5 affected fruit weight due to genetic changes. Mutation locations in different alleles resulted in varied responses between iaa9-3 and iaa9-5, such as fruit size and weight. Fruit weight was affected by the number of fruits on the plant. Under normal conditions, iaa9-5 had a higher fruit number compared with that in heat-stress condition, but it had a lower fruit size ( Figure 6). Burge et al. (1987) stated that fruit weight decreased with the increase in fruit number per vine in kiwifruit. A similar finding was reported by Puspitasari et al. (2014) who revealed that the more fruits produced, the less the individual fruit size.
IAA9 gene mutations in iaa9-3 and iaa9-5 caused a decrease in the number of seeds under normal conditions. This study was in line with the research of Liu et al. (2018) on SlARF5-6 parthenocarpic transgenic tomato, which showed a high AUX response, resulting in a lower number of seeds compared with the WT. According to Takisawa et al. (2019) low seed production was attributed to two reasons, i.e. (1) formation of pseudo-embryo from the innermost layer of the embryo sac and (2) inhibition of pollen tube elongation. A few seeds that were found in both mutants at 40°C -45°C indicated that only a few viable pollens in both mutants can fertilise.
Heat stress increases ROS, such as H 2 O 2 , accumulation within plant tissues (Suzuki and Mittler, 2006). This continuous accumulation of ROS within plant tissues damages the cell plasma membrane (Dhanda and Munjal, 2009). In this study, iaa9-3 and iaa9-5 showed a lower H 2 O 2 accumulation compared with WT-MT and higher antioxidant activities ( Figures 7A, B). Antioxidants scavenge ROS and break it down into less radical compounds that are less harmful to plant cells (Moons, 2005). The higher antioxidant activity observed in iaa9-3 and iaa9-5 leaves was likely caused by the heightened AUX response in both IAA9 mutants. Increased AUX concentration has been linked to increased antioxidant synthesis (Moons, 2005;Duan et al., 2010), DELLA protein stability (Paponov et al., 2008), and ethylene synthesis (Tognetti et al., 2012). AUX enhances antioxidant enzyme synthesis by activating the redox genes responsible for catalase, superoxide dismutase, guaiacol peroxidase, ascorbate peroxidase and glutathione-S-transferase synthesis (Tognetti et al., 2012;Sergiev et al., 2018).
In conclusion, the results showed that iaa9-3 and iaa9-5 exhibited a reduction in vegetative plant growth, delayed flowering time, increased number of flowers, ability to produce fruit and adaptability to heat-stress conditions. Thus, iaa9-3 and iaa9-5 can potentially contribute to breeding programs to generate new heat-tolerant commercial tomato cultivars.

Data availability statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Author contributions
All authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.

Funding
We thank Universitas Padjadjaran, Indonesia, for supporting this work through a grant on the scheme of Indonesian Research Collaboration year 2022 with grant number 2203/UN6.3.1/PT.00/ 2022, and the APC was funded by Universitas Padjadjaran.