A contiguous de novo genome assembly of sugar beet EL10 (Beta vulgaris L.).

IF 3.9 2区 生物学 Q1 GENETICS & HEREDITY
J Mitchell McGrath, Andrew Funk, Paul Galewski, Shujun Ou, Belinda Townsend, Karen Davenport, Hajnalka Daligault, Shannon Johnson, Joyce Lee, Alex Hastie, Aude Darracq, Glenda Willems, Steve Barnes, Ivan Liachko, Shawn Sullivan, Sergey Koren, Adam Phillippy, Jie Wang, Tiffany Liu, Jane Pulman, Kevin Childs, Shengqiang Shu, Anastasia Yocum, Damian Fermin, Effie Mutasa-Göttgens, Piergiorgio Stevanato, Kazunori Taguchi, Rachel Naegele, Kevin Dorn
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引用次数: 0

Abstract

A contiguous assembly of the inbred 'EL10' sugar beet (Beta vulgaris ssp. vulgaris) genome was constructed using PacBio long-read sequencing, BioNano optical mapping, Hi-C scaffolding, and Illumina short-read error correction. The EL10.1 assembly was 540 Mb, of which 96.2% was contained in nine chromosome-sized pseudomolecules with lengths from 52 to 65 Mb, and 31 contigs with a median size of 282 kb that remained unassembled. Gene annotation incorporating RNA-seq data and curated sequences via the MAKER annotation pipeline generated 24,255 gene models. Results indicated that the EL10.1 genome assembly is a contiguous genome assembly highly congruent with the published sugar beet reference genome. Gross duplicate gene analyses of EL10.1 revealed little large-scale intra-genome duplication. Reduced gene copy number for well-annotated gene families relative to other core eudicots was observed, especially for transcription factors. Variation in genome size in B. vulgaris was investigated by flow cytometry among 50 individuals producing estimates from 633 to 875 Mb/1C. Read-depth mapping with short-read whole-genome sequences from other sugar beet germplasm suggested that relatively few regions of the sugar beet genome appeared associated with high-copy number variation.

甜菜EL10 (Beta vulgaris L.)的连续从头基因组组装。
近交系‘EL10’甜菜(Beta vulgaris ssp)的连续组合。采用PacBio长读序列测序、BioNano光学定位、Hi-C脚手架和Illumina短读错误校正技术构建vulgaris基因组。EL10.1片段长540 Mb,其中96.2%为9个长度为52 ~ 65 Mb的染色体大小的假分子,还有31个片段未组装,中位长度为282 kb。通过MAKER注释管道,结合RNA-seq数据和精选序列的基因注释生成了24,255个基因模型。结果表明,EL10.1基因组序列与已发表的甜菜参考基因组序列高度一致。总体重复基因分析显示EL10.1几乎没有大规模的基因组内重复。与其他核心基因相比,注释良好的基因家族的基因拷贝数减少,尤其是转录因子。用流式细胞术研究了50个个体的基因组大小变异,估计值在633 ~ 875 Mb/1C之间。与其他甜菜种质的短读全基因组序列的读取深度映射表明,甜菜基因组中相对较少的区域与高拷贝数变异相关。
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来源期刊
DNA Research
DNA Research 生物-遗传学
CiteScore
6.00
自引率
4.90%
发文量
39
审稿时长
4.5 months
期刊介绍: DNA Research is an internationally peer-reviewed journal which aims at publishing papers of highest quality in broad aspects of DNA and genome-related research. Emphasis will be made on the following subjects: 1) Sequencing and characterization of genomes/important genomic regions, 2) Comprehensive analysis of the functions of genes, gene families and genomes, 3) Techniques and equipments useful for structural and functional analysis of genes, gene families and genomes, 4) Computer algorithms and/or their applications relevant to structural and functional analysis of genes and genomes. The journal also welcomes novel findings in other scientific disciplines related to genomes.
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