USDA Agricultural Research Service, Center for Grain and Animal Health Research, 1515 College Ave., Manhattan, KS 66502, USA.
All Things Bugs LLC, 755 Research Parkway, Suite 465, Oklahoma City, OK 73130, USA.
Genes (Basel). 2023 Dec 14;14(12):2209. doi: 10.3390/genes14122209.
Insects are a sustainable source of protein for human food and animal feed. We present a genome assembly, CRISPR gene editing, and life stage-specific transcriptomes for the yellow mealworm, , one of the most intensively farmed insects worldwide.
Long and short reads and long-range data were obtained from a male pupa. Sequencing transcripts from 12 life stages resulted in 279 million reads for gene prediction and genetic engineering. A unique plasmid delivery system containing guide RNAs targeting the eye color gene flanking the muscle gene promoter and EGFP marker was used in CRISPR/Cas9 transformation.
The assembly is approximately 53% of the genome size of 756.8 ± 9.6 Mb, measured using flow cytometry. Assembly was complicated by a satellitome of at least 11 highly conserved satDNAs occupying 28% of the genome. The injection of the plasmid into embryos resulted in knock-out of and knock-in of EGFP.
The genome of is longer than current assemblies (including ours) due to a substantial amount (26.5%) of only one highly abundant satellite DNA sequence. Genetic sequences and transformation tools for an insect important to the food and feed industries will promote the sustainable utilization of mealworms and other farmed insects.
昆虫是人类食物和动物饲料中可持续的蛋白质来源。我们展示了一种基因组组装、CRISPR 基因编辑和特定生命阶段转录组的方法,用于黄粉虫,这是全球养殖最广泛的昆虫之一。
从一只雄性蛹中获得了长读长和短读长以及长程数据。对 12 个生命阶段的转录物进行测序,得到了 2.79 亿个用于基因预测和遗传工程的读长。使用含有靶向眼色基因侧翼肌肉基因启动子和 EGFP 标记的向导 RNA 的独特质粒递送系统,在 CRISPR/Cas9 转化中进行了基因编辑。
组装的基因组大小约为 756.8 ± 9.6 Mb,使用流式细胞术测量。由于至少有 11 个高度保守的 satDNA 组成的卫星体占据了基因组的 28%,组装变得复杂。将质粒注射到胚胎中导致 基因敲除和 EGFP 基因敲入。
由于只有一种高度丰富的卫星 DNA 序列数量很大(26.5%),所以 的基因组比当前的组装(包括我们的组装)都要长。对于食品和饲料工业中重要的昆虫来说,遗传序列和转化工具将促进黄粉虫和其他养殖昆虫的可持续利用。