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Heat map and abundance patterns of differentially accumulated proteins in the eighth internode of the hybrids and parental lines. Note: Differences in accumulation are presented as a continuous range of colours. Red corresponds to the maximum accumulation (grey value: 449574); green corresponds to the minimum accumulation (grey value: 0); and yellow corresponds to the median accumulation (grey value: 224787). 

Heat map and abundance patterns of differentially accumulated proteins in the eighth internode of the hybrids and parental lines. Note: Differences in accumulation are presented as a continuous range of colours. Red corresponds to the maximum accumulation (grey value: 449574); green corresponds to the minimum accumulation (grey value: 0); and yellow corresponds to the median accumulation (grey value: 224787). 

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Ear height is an important maize morphological trait that influences plant lodging resistance in the field, and is based on the number and length of internodes under the ear. To explore the effect of internodes on ear height, the internodes under the ear were analysed in four commercial hybrids (Jinsai6850, Zhengdan958, Xundan20, and Yuyu22) from d...

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... Yuyu22 (54.11 and 52.39%) ( Fig. 2; Table S2). In other words, the extent of the heterosis was inconsistent with the heterosis performance for the extended internodes, ear height, and plant height. (Fig. 3). Moreover, 15, 16, 22, and 13 pro- tein spots with >1.5-fold difference (P < 0.05) were excised from gels and identified by MS, respectively (Fig. 4, Table S4). The majority (54/66) of these protein spots were additively accumulated in the four hybrids, espe- cially in Xundan20 (21/22). The non-additively accumulated protein spots exhibited different patterns in the four hybrids, even for the hybrids in the same heterotic group [i.e., Zhengdan958 (+, ++, and +−) and Xundan20 (−)] ...
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... (Fig. 4, Table S4). The majority (54/66) of these protein spots were additively accumulated in the four hybrids, espe- cially in Xundan20 (21/22). The non-additively accumulated protein spots exhibited different patterns in the four hybrids, even for the hybrids in the same heterotic group [i.e., Zhengdan958 (+, ++, and +−) and Xundan20 (−)] (Fig. 4, Table S4). The 66 protein spots (peptides are listed in Table S5) were represented by 46 GenBank accessions. Additionally, some GenBank accessions were identified in the same hybrid twice with different accumulation patterns, likely because of distinct post-translational modifications of the correspond- ing proteins. GenBank accessions ...
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... in all hybrids. However, gi|195613358 accumulated dif- ferently in the four hybrids (protein spots 2 and 3 in Jinsai6850, 16 in Zhengdan958, 42 in Xundan20, and 63 in Yuyu22), while the accumulation patterns for gi|226499080 were similar in the four hybrids (protein spot 10 in Jinsai6850, 27 in Zhengdan958, 50 in Xundan20, and 65 in Yuyu22) (Fig. 4, Table S4). organismal systems, cellular processes, and unknown (Fig. 5, Table S6). Metabolism was the largest category, with 74% (49/66) of the differentially accumulated protein spots, implying metabolic activities are critical for internode development and heterosis. The metabolism category was further divided into seven subcategories, ...
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... effects on gene expression or protein accumulation differentially contribute to the heterosis of a particular trait at specific developmental stages 2 . The overwhelming additive accumulation of differentially accumulated proteins in the four hybrids was associated with a non-additive effect on the heterosis performance of the eighth internode (Fig. 4, Tables S2 and 4). Similar results were also reported for maize embryos at 6 days after fertilisation 25 , while another study concluded that the moderate transcriptional expression of the SINGLE FLOWER TRUSS locus could result in an over-dominant effect on yield 26 . These results proved that an additive interaction at the ...

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... Plant height (PH) is one of the most important traits for grain yield in breeding programs for maize, and is highly heritable despite its complex, polygenic nature [61,62]. On the other hand, certain authors pointed out that plant height, measured over time, can provide an assessment of physiology and critical genetic traits, as well as the influence of environmental conditions on plant performance [63][64][65][66][67][68]. Plant height is associated with the grain number per spike, biomass production, and harvest index, and thus increases grain yield and quality [69]. ...
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... The use of Paclobutrazol is reported to be able to shorten the segment (Wen et al., 2013) due to the suppression of kaurene, which inhibits gibberellin biosynthesis so that cell division morphologically decreases. Paclobutrazol could also suppress the effect of IAA in plants (Soumya et al., 2017), while IAA could induce internode elongation (Chen et al., 2018). ...
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... The most critical agronomic traits of maize are plant height, ear height, and stem diameter, all of which are directly related to crop lodging resistance, biomass production, and yield [35][36][37][38]. In general, different effects were observed for each of the agronomic traits of maize (plant height, ear height, and stem diameter) when N fertilization was applied, as shown in Figure 2. In comparison with the zero-N treatment, the NPK fertilizer application only improved maize ear height, which resulted in poor maize lodging resistance. ...
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... Auxin is known as the 'growth' hormone because, via a combination of local biosynthesis and transport (Brumos et al., 2018), it is involved in almost all aspects of plant growth and development (reviewed in Enders & Strader, 2015;Chen et al., 2018;reviewed in Dong & Huang, 2018;reviewed in Luo et al., 2018;reviewed in Basunia & Nonhebel, 2019;Bernardi et al., 2019;Chen & McClung, 2019). These processes consume a substantial amount of the cellular energy budget, but how does auxin influence energy generation or use to enable its growth-promoting effects? ...
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In a large number of plant species, including maize, different phenotypic traits have undergone major changes through the breeding process, resulting in the creation of varieties and hybrids of good agronomic performance. This study aimed to examine the variability of the plant height (PH) and plant height to the uppermost ear (EH) of maize top cross hybrids obtained from crossing 31 local landraces with three genetically divergent testers (L217, L73B013 and L255/75-5). Top cross hybrids were tested in a two-year experiment, at four locations, in two replicates. The grand mean of top cross hybrids for PH and EH were 255.8 cm and 101.8 cm. Analysis of variance showed that all sources of variation (environment - year × location (E), landrace (B), tester effect (A), as well as their interactions) were highly significant (p≤0.01), except for triple interaction (A × B × E). The coefficients of variation for the PH and EH were 4.76% and 8.87%. A highly significant correlation was found between the examined traits (r=0.785; p <0.01). Linear regression of PH and EH shows that the increase of EH by 0.5 cm is followed by the 1 cm of PH increase. Based on the results, the general combining ability (GCA) of landraces for the examined traits, is under the influence of the additive effect of genes, i.e. tall landraces per se in crosses with all three testers give tall hybrids and inversely. In maize production, a trait of interest is the small EH/PH ratio. Landraces MB1960, MB642 and MB1890 showed the best GCA for a given trait, so they can serve as sources of a given trait in pre-breeding programmes.
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... The differences in maize plant height and ear height have been shown to be caused by differences in both the total internode number and internode length, and differences in both the internode number and internode length below the primary ear, respectively (Zhu et al., 2013;Chen et al., 2018). For some hybrids, a significant difference in ear height is caused by longer internodes, especially between the sixth and seventh internodes and between the seventh and eighth internodes (Chen et al., 2018). For maize cultivars released from the 1950s to the 2010s in China, the internode number per plant was not found to change significantly with cultivar replacement, the lengths of the first to eighth internodes below the ear slightly decreased, and the lengths of the ninth to sixteenth internodes increased (Ma et al., 2014b). ...
... Differences in the heights of maize plants may be due to differences in the internode length, differences in the internode number, or both. Chen et al. (2018) reported that, for extended internodes, a significant difference in ear height was contributed by longer internodes, especially between the sixth and seventh internodes and between the seventh and eighth internodes. In this study, the differences in plant height between different cultivars were mainly due to differences in the mean internode length, and the differences in ear height were mainly due to the differences in the internode number below the primary ear (Fig. 3A, B). ...
Article
Maize (Zea mays L.) height morphological traits (i.e., plant height, ear height, and ear ratio) are important parts of maize plant type structure and have played an important role in the improvement of maize lodging resistance and historical increases in grain yield. In this study, field experiments were conducted from 2013 to 2016 at 23 sites in China between 26°30′–46°45′ N latitude and 81°19′–130°16′ E longitude. Five common cultivars and one planting density (6.0 × 10⁴ plants ha⁻¹) were used to determine the amplitude of variation in maize height morphological traits for the same cultivars and the differences in maize height morphological traits between different cultivars. The results elucidated that the main factors affecting maize height morphological traits and characterize the responses of aboveground dry matter (DM) and grain yield to differences in plant height over a wide range of environmental conditions. The findings showed that for cultivars Denghai 11 (DH11), Nonghua 101 (NH101), Xianyu 335 (XY335), Zhengdan 958 (ZD958), and Zhongdan 909 (ZD909), plant heights ranged from 233.1 to 395.3, 240.7–389.6, 246.0–370.0, 201.8–327.3, and 199.1–346.7 cm, respectively, ear heights ranged from 93.2 to 186.0, 64.6–146.5, 70.5–170.0, 71.1–168.3, and 66.2–150.7 cm, respectively, and ear ratios ranged from 0.33 to 0.49, 0.26–0.47, 0.26–0.49, 0.35–0.54, and 0.32–0.50, across all sites and years. Furthermore, the mean internode length and mean internode length below the primary ear were found to be the main contributors to the differences in plant height and ear height, respectively. Additionally, the results of stepwise regression indicated that both plant height and ear height were mainly affected by photoperiod and minimum temperature but the major climatic variables influencing ear ratio varied among different cultivars. Moreover, a linear model showed that, for every 10 cm increase in maize plant height, the DM at silking, DM at physiological maturity, and grain yield increased by approximately 0.41 t ha⁻¹, 0.87 t ha⁻¹, and 0.38 t ha⁻¹, respectively.
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... Moreover, heterosis is believed to be trait-dependent, suggesting that the fundamental mechanisms are effective within specific traits (Baranwal et al., 2012;Kaeppler, 2012). The intensity of heterosis, in fact, depends on genome structural variations (Jung and Casler, 2006;Zhang et al., 2007), epigenetic modifications, post-transcriptional events, and specific protein functions (Chen et al., 2018). Thus, of all biochemical events contributing to heterosis, specific protein expressions and functions involved in heterosis are critical to be characterized. ...
... Thus, of all biochemical events contributing to heterosis, specific protein expressions and functions involved in heterosis are critical to be characterized. For example, in a study with maize plants, Chen et al. (2018) detected 66 proteins and they categorized all proteins into six distinct classes, i.e. genetic information processing, organism structures, cellular processes, processing of environmental information, metabolism, and unknown proteins. ...
... Proteins in BXs and phenylpropanoid metabolic pathways were detected in maize plants, which can affect polar auxin transport and biosynthesis of IAA in internode development. Furthermore, the IAA amount was negatively associated, while positively correlated with the eighth internode length, but was positively correlated with the heterosis value of the eighth internode length (Chen et al., 2018). Our findings also showed that all of the proteins detected in the maize hybrids had positive heterosis (Fig. 4). ...
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In the current research, the pattern of expression of hybrid proteins in the leaves of two maize inbred lines, B73 (♀) and MO17 (♂), as well as the F1, SC704, was investigated using 2-DE. A hydroponic experiment was conducted in a greenhouse. Leaf tissue proteome analysis of the two parents and their F1 showed that seven reproducible protein spots had significant modifications, revealing their up-regulation. These seven differentially expressed proteins were categorized into three functional groups, including the defense system, regulator, and energy metabolism. Proteomic analysis indicated that all proteins of the mid parent had prominent expression compared with that of the parental proteins. It can be concluded that in the significant vigor of hybrid SC704 was due to enhanced expression of proteins involved in defense, regulation, and energy metabolism.