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Leaf width is a key determinant of planting density and photosynthetic efficiency. In an effort to determine which genes regulate maize plant leaf width, we performed a genome-wide association study (GWAS) of 1.49 × 106 single nucleotide polymorphisms (SNPs) in 80 sequenced backbone inbred maize lines in Jilin Province, China, based upon phenotypic leaf width data from two years. In total, 14 SNPs were identified as being significantly related to leaf width (p < 0.000001), with these SNPs being located on chromosomes 1, 2, 3, 5, 6, 7, 8, and 9. A total of five candidate genes were identified within a mean linkage disequilibrium (LD) distance of 9.7 kb, with a significant SNP being identified within the Zm00001d044327 candidate gene. RNA was then isolated from 12 different inbred maize lines from this GWAS study cohort and was used to conduct qPCR analyses which revealed significant differences in Zm00001d044327 expression among strains exhibiting significant differences in leaf width. Based on an assessment of EMS mutant lines harboring a conserved amino acid stop mutation and two non-synonymous mutations in Zm00001d044327 that exhibited a narrow leaf width, these data suggested that Zm00001d044327 is a key regulator of maize leaf width.

Plant height and leaf morphology are considered complex agronomy traits; both are significantly related to nutrient utilization, lodging resistance, and photosynthetic efficiency, which ultimately affect biomass and yield. However, the molecular mechanism of leaf morphogenesis is still unclear. WOX is a group of plant-specific transcription factor families that regulate growth and development, cell division, and differentiation in plants. In the present study, we identified and characterized the m-876 mutant in barley (Hordeum vulgare L.), which exhibited an extreme reduction in leaf width and plant height. Using a map-based cloning strategy, the m-876 mutant was narrowed down to an 11.4 Mb genomic interval on the long arm of chromosome 5. By analyzing the gene annotation information and nucleotide sequences, we found that HvWOX3A (HORVU.MOREX.r3.5HG0467090) had a G-to-A substitution at the second exon in the m-876 mutant, resulting in a change of the coding amino acid from Tryptophan to a premature stop codon at the 200th amino acid position. Remarkably, the mutation of the HvWOX3A gene leads to changes in gene expression in the m-876 mutant. Collectively, our results indicate that the loss function of the HORVU.MOREX.r3.5HG0467090 gene might be responsible for the phenotypic variation in barley mutants.

Maize is an important food and feed crop. Under limited arable land area, the cultivation of high-density-tolerance crops is a key factor in promoting yield improvement. Leaf width and stalk strength are important influences on density tolerance in maize. However, no comprehensive transcriptomic analysis has focused on maize’s leaf width and stalk strength formation mechanisms. In this study, comparative transcriptomic analyses demonstrated that significant transcriptome changes occurred regarding leaf width and stalk strength of narrow-leaved and wide-leaved maize inbred lines, with a total of 5001 differentially expressed genes (DEGs) identified. Enrichment analysis showed that phenylpropanoid biosynthesis, starch and sucrose metabolism, phytohormone signaling, amino acid metabolism, and brassinosteroid biosynthesis were significantly correlated with the formation of maize leaf shape and stalk strength and that the genes in these pathways were primarily involved in cell wall formation. Weighted gene co-expression network analysis identified 2 modules significantly correlated with leaf width and stalk strength, from which 11 hub genes were further identified. The 11 leaf and stem development genes in different pathways were validated using qRT-PCR. These findings can provide a theoretical basis for the mechanism of narrow-leaf and high-strength stalk formation in high-density-tolerance maize and contribute to the proposal of a breeding strategy for yield improvement.

Leaf width is a key determinant of planting density and photosynthetic efficiency. In an effort to determine which genes regulate maize plant leaf width, we performed a genome-wide association study (GWAS) of 1.49 × 106 single nucleotide polymorphisms (SNPs) in 80 sequenced backbone inbred maize lines in Jilin Province, China, based upon phenotypic leaf width data from two years. In total, 14 SNPs were identified as being significantly related to leaf width ( p < 0.000001), with these SNPs being located on chromosomes 1, 2, 3, 5, 6, 7, 8, and 9. A total of five candidate genes were identified within a mean linkage disequilibrium (LD) distance of 9.7 kb, with a significant SNP being identified within the Zm00001d044327 candidate gene. RNA was then isolated from 12 different inbred maize lines from this GWAS study cohort and was used to conduct qPCR analyses which revealed significant differences in Zm00001d044327 expression among strains exhibiting significant differences in leaf width. Based on an assessment of EMS mutant lines harboring a conserved amino acid stop mutation and two non-synonymous mutations in Zm00001d044327 that exhibited a narrow leaf width, these data suggested that Zm00001d044327 is a key regulator of maize leaf width.

Leaf shape and size can vary between hybrids and their parents. However, this has seldom been quantitatively tested. Photinia × fraseri is an important landscaping plant in East Asia as a hybrid between evergreen shrubs P. glabra and P. serratifolia. Its leaf shape looks like that of P. serratifolia. To investigate leaf shape, we used a general equation for calculating the leaf area (A) of broad-leaved plants, which assumes a proportional relationship between A and product of lamina length (L) and width (W). The proportionality coefficient (which is referred to as the Montgomery parameter) serves as a quantitative indicator of leaf shape, because it reflects the proportion of leaf area A to the area of a rectangle with L and W as its side lengths. The ratio of L to W, and the ellipticalness index were also used to quantify the complexity of leaf shape for elliptical leaves. A total of >4000 leaves from P. × fraseri and P. serratifolia (with >2000 leaves for each taxon) collected on a monthly basis was used to examine: (i) whether there is a significant difference in leaf shape between the two taxa, and (ii) whether there is a monotonic or parabolic trend in leaf shape across leaf ages. There was a significant difference in leaf shape between the two taxa (p < 0.05). Although there were significant differences in leaf shape on a monthly basis, the variation in leaf shape over time was not large, i.e., leaf shape was relatively stable over time for both taxa. However, the leaf shape of the hybrid was significantly different from its parent P. serratifolia, which has wider and more elliptical leaves than the hybrid. This work demonstrates that variations in leaf shape resulting from hybridization can be rigorously quantified and compared among species and their hybrids. In addition, this work shows that leaf shape does not changes as a function of age either before or after the full expansion of the lamina.

Many plant species produce ovate leaves, but there is no general parametric model for describing this shape. Here, we used two empirical nonlinear equations, the beta and Lobry–Rosso–Flandrois (LRF) equations, and their modified forms (referred to as the Mbeta and MLRF equations for convenience), to generate bilaterally symmetrical curves along the x-axis to form ovate leaf shapes. In order to evaluate which of these four equations best describes the ovate leaf shape, we used 14 leaves from 7 Neocinnamomum species (Lauraceae) and 72 leaves from Chimonanthus praecox (Calycanthaceae). Using the AIC and adjusted root mean square error to compare the fitted results, the modified equations fitted the leaf shapes better than the unmodified equations. However, the MLRF equation provided the best overall fit. As the parameters of the MLRF equation represent leaf length, maximum leaf width, and the distance from leaf apex to the point associated with the maximum leaf width along the leaf length axis, these findings are potentially valuable for studying the influence of environmental factors on leaf shape, differences in leaf shape among closely related plant species with ovate leaf shapes, and the extent to which leaves are bilaterally symmetrical. This is the first work in which temperature-dependent developmental equations to describe the ovate leaf shape have been employed, as previous studies lacked similar leaf shape models. In addition, prior work seldom attempted to describe real ovate leaf shapes. Our work bridges the gap between theoretical leaf shape models and empirical leaf shape indices that cannot predict leaf shape profiles.

A model for estimating the area of individual leaves (LA) by employing their dimensions was developed for chrysanthemum. Further hypotheses were tested: (a) LA estimation is improved by considering blade length (Lb) rather than leaf length (L), and (b) a reasonable LA estimation can be attainable by considering L in conjunction to a shape trait, which is cultivar dependent. For the model development, six cultivars were employed (1500 leaves in total), while for model validation, an independent set of nine cultivars was utilized (1125 leaves in total). Several characteristics were digitally assessed in fully expanded leaves which included petiole length, leaf L, width (W), perimeter, shape traits (aspect ratio, circularity, roundness, solidity), together with LA. LA estimation was more accurate by considering both L and W, as compared to a single dimension. A linear model, employing the product of L by W as independent variable, provided the most accurate LA estimation (R2 = 0.84). The model validation indicated a highly significant correlation between computed and measured LA (R2 = 0.88). Replacing L by Lb reasonably predicted LA (R2 = 0.832) but at some expense of accuracy. Contrary to expectation, considering L (or W) and a cultivar-specific shape trait generally led to poor LA estimations.

Leaf area is among the most important leaf functional traits, and it determines leaf temperature and alters light harvesting. The calculation of individual leaf area is the basis of calculating the leaf area index (i.e., the total leaf area per unit ground area) that is directly associated with the ability of plants to intercept light for photosynthesis. It is valuable to provide a fast and reliable approach to measuring leaf area. Here, we examined the validity and calculation accuracy of the Montgomery equation (ME), which describes the area of a leaf as a product of leaf length, width and a specific coefficient referred to as the Montgomery parameter, MP. Using ME, we calculated leaf areas of different age groups of bamboo culms. For most broad-leaved plants, leaf area is proportional to the product of leaf length and width, and MP falls within a range of 1/2 to π/4, depending on leaf shape. However, it is unknown whether there is an intra-specific variation in MP resulting from age structure and whether such a variation can significantly reduce the predictability of ME in calculating leaf area. This is relevant as a population of perennial plants usually composes of different age groups. We used Moso bamboos as model as this species is of ecological and economic importance in southern China, and pure stands can cover six to seven plant age groups. We used five age groups of moso bamboo and sampled 260–380 leaves for each group to test whether ME holds true for each group and all groups combined, whether there are significant differences in MP among different age groups, and whether the differences in MP can lead to large prediction errors for leaf area. We observed that for each age group and all groups combined, there were significant proportional relationships between leaf area and the product of leaf length and width. There were small but significant differences in MP among the five age groups (MP values ranged from 0.6738 to 0.7116 for individual plant ages; MP = 0.6936 for all age groups combined), which can be accounted for by the minor intergroup variation of leaf shape (reflected by the leaf width/length ratio). For all age classes, MP estimated for the pooled data resulted in

Leaf shape and size can vary between hybrids and their parents. However, this has seldom been quantitatively tested. Photinia × fraseri is an important landscaping plant in East Asia as a hybrid between evergreen shrubs P. glabra and P. serratifolia. Its leaf shape looks like that of P. serratifolia. To investigate leaf shape, we used a general equation for calculating the leaf area (A) of broad-leaved plants, which assumes a proportional relationship between A and product of lamina length (L) and width (W). The proportionality coefficient (which is referred to as the Montgomery parameter) serves as a quantitative indicator of leaf shape, because it reflects the proportion of leaf area A to the area of a rectangle with L and W as its side lengths. The ratio of L to W, and the ellipticalness index were also used to quantify the complexity of leaf shape for elliptical leaves. A total of >4000 leaves from P. × fraseri and P. serratifolia (with >2000 leaves for each taxon) collected on a monthly basis was used to examine: (i) whether there is a significant difference in leaf shape between the two taxa, and (ii) whether there is a monotonic or parabolic trend in leaf shape across leaf ages. There was a significant difference in leaf shape between the two taxa (p < 0.05). Although there were significant differences in leaf shape on a monthly basis, the variation in leaf shape over time was not large, i.e., leaf shape was relatively stable over time for both taxa. However, the leaf shape of the hybrid was significantly different from its parent P. serratifolia, which has wider and more elliptical leaves than the hybrid. This work demonstrates that variations in leaf shape resulting from hybridization can be rigorously quantified and compared among species and their hybrids. In addition, this work shows that leaf shape does not changes as a function of age either before or after the full expansion of the lamina.