BackgroundMost published genome sequences are drafts, and most are dominated by computational gene prediction. Draft genomes typically incorporate considerable sequence data that are not assigned to chromosomes, and predicted genes without quality confidence measures. The current Actinidia chinensis (kiwifruit) ‘Hongyang’ draft genome has 164 Mb of sequences unassigned to pseudo-chromosomes, and omissions have been identified in the gene models.ResultsA second genome of an A. chinensis (genotype Red5) was fully sequenced. This new sequence resulted in a 554.0 Mb assembly with all but 6 Mb assigned to pseudo-chromosomes. Pseudo-chromosomal comparisons showed a considerable number of translocation events have occurred following a whole genome duplication (WGD) event some consistent with centromeric Robertsonian-like translocations. RNA sequencing data from 12 tissues and ab initio analysis informed a genome-wide manual annotation, using the WebApollo tool. In total, 33,044 gene loci represented by 33,123 isoforms were identified, named and tagged for quality of evidential support. Of these 3114 (9.4%) were identical to a protein within ‘Hongyang’ The Kiwifruit Information Resource (KIR v2). Some proportion of the differences will be varietal polymorphisms. However, as most computationally predicted Red5 models required manual re-annotation this proportion is expected to be small. The quality of the new gene models was tested by fully sequencing 550 cloned ‘Hort16A’ cDNAs and comparing with the predicted protein models for Red5 and both the original ‘Hongyang’ assembly and the revised annotation from KIR v2. Only 48.9% and 63.5% of the cDNAs had a match with 90% identity or better to the original and revised ‘Hongyang’ annotation, respectively, compared with 90.9% to the Red5 models.ConclusionsOur study highlights the need to take a cautious approach to draft genomes and computationally predicted genes. Our use of the manual annotation tool WebApollo facilitated manual checking and correction of gene models enabling improvement of computational prediction. This utility was especially relevant for certain types of gene families such as the EXPANSIN like genes. Finally, this high quality gene set will supply the kiwifruit and general plant community with a new tool for genomics and other comparative analysis.Electronic supplementary materialThe online version of this article (10.1186/s12864-018-4656-3) contains supplementary material, which is available to authorized users.
We present a draft assembly of the genome of European pear (Pyrus communis) ‘Bartlett’. Our assembly was developed employing second generation sequencing technology (Roche 454), from single-end, 2 kb, and 7 kb insert paired-end reads using Newbler (version 2.7). It contains 142,083 scaffolds greater than 499 bases (maximum scaffold length of 1.2 Mb) and covers a total of 577.3 Mb, representing most of the expected 600 Mb Pyrus genome. A total of 829,823 putative single nucleotide polymorphisms (SNPs) were detected using re-sequencing of ‘Louise Bonne de Jersey’ and ‘Old Home’. A total of 2,279 genetically mapped SNP markers anchor 171 Mb of the assembled genome. Ab initio gene prediction combined with prediction based on homology searching detected 43,419 putative gene models. Of these, 1219 proteins (556 clusters) are unique to European pear compared to 12 other sequenced plant genomes. Analysis of the expansin gene family provided an example of the quality of the gene prediction and an insight into the relationships among one class of cell wall related genes that control fruit softening in both European pear and apple (Malus×domestica). The ‘Bartlett’ genome assembly v1.0 (http://www.rosaceae.org/species/pyrus/pyrus_communis/genome_v1.0) is an invaluable tool for identifying the genetic control of key horticultural traits in pear and will enable the wide application of marker-assisted and genomic selection that will enhance the speed and efficiency of pear cultivar development.
Black raspberry (Rubus occidentalis L.) is a niche fruit crop valued for its flavor and potential health benefits. The improvement of fruit and cane characteristics via molecular breeding technologies has been hindered by the lack of a high-quality reference genome. The recently released draft genome for black raspberry (ORUS 4115-3) lacks assembly of scaffolds to chromosome scale. We used high-throughput chromatin conformation capture (Hi-C) and Proximity-Guided Assembly (PGA) to cluster and order 9650 out of 11,936 contigs of this draft genome assembly into seven pseudo-chromosomes. The seven pseudo-chromosomes cover ~97.2% of the total contig length (~223.8 Mb). Locating existing genetic markers on the physical map resolved multiple discrepancies in marker order on the genetic map. Centromeric regions were inferred from recombination frequencies of genetic markers, alignment of 303 bp centromeric sequence with the PGA, and heat map showing the physical contact matrix over the entire genome. We demonstrate a high degree of synteny between each of the seven chromosomes of black raspberry and a high-quality reference genome for strawberry (Fragaria vesca L.) assembled using only PacBio long-read sequences. We conclude that PGA is a cost-effective and rapid method of generating chromosome-scale assemblies from Illumina short-read sequencing data.
-Coarse root systems of four different fruit tree species from southern Africa were completely excavated and semi-automatically digitized. Spatial distributions of root length were determined from the digitally-reconstructed branching systems. Furthermore, the fractal characteristic of the coarse root systems was shown by determining the box-counting dimensions. These quantitative methods revealed architectural differences between the species, probably due to different ecophysiological strategies. For fine root samples, which were taken before digging out the whole systems, fractal analysis of the planar projections showed no significant inter-species differences. Methodologically, the study underlines the usefulness of digital 3-D reconstruction in root research. root / digital reconstruction / fractal / architectural analysis / coarse root Résumé -Structures et dimensions fractales des systèmes racinaires provenant de quatre espèces d'arbres fruitiers de Botswana. Des systèmes de grosses racines, provenant de quatre espèces différentes d'arbres fruitiers d'Afrique du Sud, ont été complètement déterrés et digitalisés semi-automatiquement. Les distributions spatiales des longueurs de racines ont été calculées à partir des maquettes informatiques reconstituées. En outre, le caractère fractal des systèmes de grosses racines a été prouvé par une déter-mination de dimensions utilisant la méthode du comptage de boites. Ces méthodes quantitatives révèlent des différences architecturales entre les espèces, résultant probablement de différentes stratégies écophysiologiques. Pour les échantillons de racines fines, obtenus avant l'excavation des systèmes complets, l'analyse fractale des projections planes n'a pas montré de différences significatives entre les espèces. Concernant la méthode, l'étude fait apparaître l'apport de la reconstruction digitale 3-D dans le domaine de la recherche sur les appareils racinaires. racine / reconstruction digitale / fractal / analyse architectural / racine gros
In recent years, many different advanced mathematical models and simulation systems for tree and forest growth have been developed. We show a possibility to extend analysis tools for measured and simulated plants using a data interface between the simulation model LIGNUM and the multifunctional software system GROGRA. Both systems were developed by different teams. To demonstrate the enhanced possibilities for analyzing a LIGNUM tree, several examples are given. In these examples three different approaches for analysis are applied to measured and simulated trees: Fractal dimension, deduction of tapering laws, and water potential patterns obtained from simulation of waterflow by the specialized software HYDRA. Conclusions for the interfacing and comparison of different modelling tools are drawn.
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