Molecular identification of a peroxidase gene controlling body size in the entomopathogenic nematode Steinernema hermaphroditum.

IF 3.3 3区 生物学 Genetics Pub Date : 2023-12-11 DOI:10.1093/genetics/iyad209
Hillel T Schwartz, Chieh-Hsiang Tan, Jackeline Peraza, Krystal Louise T Raymundo, Paul W Sternberg
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Abstract

The entomopathogenic nematode Steinernema hermaphroditum was recently rediscovered and is being developed as a genetically tractable experimental system for the study of previously unexplored biology, including parasitism of its insect hosts and mutualism with its bacterial endosymbiont Xenorhabdus griffiniae. Through whole-genome re-sequencing and genetic mapping we have for the first time molecularly identified the gene responsible for a mutationally defined phenotypic locus in an entomopathogenic nematode. In the process we observed an unexpected mutational spectrum following EMS mutagenesis in this species. We find that the ortholog of the essential C. elegans peroxidase gene skpo-2 controls body size and shape in S. hermaphroditum. We confirmed this identification by generating additional loss-of-function mutations in the gene using CRISPR-Cas9. We propose that the identification of skpo-2 will accelerate gene targeting in other Steinernema entomopathogenic nematodes used commercially in pest control, as skpo-2 is X-linked and males hemizygous for loss of its function can mate, making skpo-2 an easily recognized and maintained marker for use in co-CRISPR.
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控制昆虫病原线虫 Steinernema hermaphroditum 体型的过氧化物酶基因的分子鉴定。
最近重新发现了昆虫病原线虫 Steinernema hermaphroditum,并将其开发为一个遗传上可控的实验系统,用于研究以前未曾探索过的生物学,包括其对昆虫宿主的寄生以及与细菌内共生体 Xenorhabdus griffiniae 的互生关系。通过全基因组重测序和基因图谱绘制,我们首次在昆虫病原线虫中分子鉴定出了负责突变定义表型位点的基因。在此过程中,我们观察到该物种在 EMS 诱变后出现了意想不到的突变谱。我们发现,在雌雄同体中,重要的秀丽隐杆线虫过氧化物酶基因 skpo-2 的直向同源物控制着体型和形状。我们利用 CRISPR-Cas9 在该基因中产生了更多的功能缺失突变,从而证实了这一鉴定结果。我们认为,skpo-2 的鉴定将加速其他用于害虫防治的 Steinernema 昆虫致病线虫的基因靶向,因为 skpo-2 是 X 连锁的,其功能缺失的雄性可进行交配,这使得 skpo-2 成为一个易于识别和维护的标记,可用于共 CRISPR。
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来源期刊
Genetics
Genetics 生物-遗传学
CiteScore
6.20
自引率
6.10%
发文量
177
期刊介绍: GENETICS is published by the Genetics Society of America, a scholarly society that seeks to deepen our understanding of the living world by advancing our understanding of genetics. Since 1916, GENETICS has published high-quality, original research presenting novel findings bearing on genetics and genomics. The journal publishes empirical studies of organisms ranging from microbes to humans, as well as theoretical work. While it has an illustrious history, GENETICS has changed along with the communities it serves: it is not your mentor''s journal. The editors make decisions quickly – in around 30 days – without sacrificing the excellence and scholarship for which the journal has long been known. GENETICS is a peer reviewed, peer-edited journal, with an international reach and increasing visibility and impact. All editorial decisions are made through collaboration of at least two editors who are practicing scientists. GENETICS is constantly innovating: expanded types of content include Reviews, Commentary (current issues of interest to geneticists), Perspectives (historical), Primers (to introduce primary literature into the classroom), Toolbox Reviews, plus YeastBook, FlyBook, and WormBook (coming spring 2016). For particularly time-sensitive results, we publish Communications. As part of our mission to serve our communities, we''ve published thematic collections, including Genomic Selection, Multiparental Populations, Mouse Collaborative Cross, and the Genetics of Sex.
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