The homeobox gene Distal-less is critical for the development of adult body appendages in Bombyx mori.

IF 2.3 2区 农林科学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Guan Man, Peilin Guo, Yutong Liu, Hongxia Kang, Kai Chen, Ye Yu, Anjiang Tan
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引用次数: 0

Abstract

The development of adult body appendages is critical for insects. The homeobox gene Distal-less (Dll) is known for its role in proximodistal patterning, and its role in the development of the appendage has been well studied in the model organism Drosophila melanogaster. However, the biological function of Dll in other insects still remains to be further verified. In this study, we investigated the biological function of Dll in the lepidoptera model insect Bombyx mori. Similar to the expression patterns observed in D. melanogaster, BmDll was highly expressed in the tibia and tarsus of the legs. The BmDll mutants obtained through the binary transgenic CRISPR/Cas9 system appeared to thrive normally and no apparent deleterious phenotypes were observed throughout the embryonic and larval stages. Nevertheless, mutants exhibited severe defects in the development of the appendage, especially at the distal end of legs, from pupal stage to adult stage. RNA-seq analysis revealed that metabolism pathways, extracellular matrix (ECM)-receptor interaction and structural constituent of the cuticle were dysregulated in mutant silkworms. Our study provided genetic evidence that Dll plays an important role in the development of B. mori adult body appendages.

同源盒基因远端缺失是家蚕成体附属物发育的关键基因。
成体附属物的发育对昆虫来说是至关重要的。同源盒基因远端缺失(Dll)因其在近端远端模式中的作用而闻名,其在模式生物黑腹果蝇(Drosophila melanogaster)附属物发育中的作用已经得到了很好的研究。然而,Dll在其他昆虫中的生物学功能仍有待进一步验证。在本研究中,我们研究了Dll在鳞翅目模式昆虫家蚕中的生物学功能。与在黑腹龙中观察到的表达模式相似,bmll在腿的胫骨和跗骨中高度表达。通过CRISPR/Cas9二元转基因系统获得的BmDll突变体在胚胎和幼虫阶段似乎正常生长,没有观察到明显的有害表型。然而,从蛹期到成虫期,突变体在附属物的发育中表现出严重的缺陷,尤其是在腿的远端。RNA-seq分析显示,突变家蚕的代谢途径、细胞外基质(ECM)受体相互作用和角质层结构成分均发生了异常。本研究提供了遗传证据,证明Dll在家蚕成体附属物发育中起重要作用。
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来源期刊
Insect Molecular Biology
Insect Molecular Biology 生物-昆虫学
CiteScore
4.80
自引率
3.80%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Insect Molecular Biology has been dedicated to providing researchers with the opportunity to publish high quality original research on topics broadly related to insect molecular biology since 1992. IMB is particularly interested in publishing research in insect genomics/genes and proteomics/proteins. This includes research related to: • insect gene structure • control of gene expression • localisation and function/activity of proteins • interactions of proteins and ligands/substrates • effect of mutations on gene/protein function • evolution of insect genes/genomes, especially where principles relevant to insects in general are established • molecular population genetics where data are used to identify genes (or regions of genomes) involved in specific adaptations • gene mapping using molecular tools • molecular interactions of insects with microorganisms including Wolbachia, symbionts and viruses or other pathogens transmitted by insects Papers can include large data sets e.g.from micro-array or proteomic experiments or analyses of genome sequences done in silico (subject to the data being placed in the context of hypothesis testing).
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