4.7 Article

Identification and functional analysis of two potential RNAi targets for chitin degradation in Holotrichia parallela Motschulsky (Insecta Coleoptera)

期刊

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.pestbp.2022.105257

关键词

Holotrichia parallela; NAG and NAGK; RNA interference; Chitin

资金

  1. earmarked fund for CARS Scientific Research Project of Education Department of Hebei
  2. National Natural Science Foundation of China
  3. Foundation of Graduate School of the Chinese Academy of Agricultural Sciences (CAAS)
  4. [QN2020119]
  5. [31471775]
  6. [1610042022005]

向作者/读者索取更多资源

Chitin metabolism enzymes, specifically NAG and NAGK, play important roles in the degradation and conversion of chitin. In this study, NAG and NAGK genes were identified and their spatiotemporal expression patterns were investigated in Holotrichia parallela larvae. Silencing of HpNAG and HpNAGK resulted in a significant RNAi effect and inhibited larval growth. The study also showed that silencing these genes affected the expression levels of chitin metabolism-related genes and reduced the thickness and chitin content of the cuticle.
Chitin metabolism enzymes are safe and desirable targets for pest management. beta-N-acetylglucosaminidase (NAG) and N-acetylglucosamine kinase (NAGK) are involved in chitin degradation. NAG is the main glycosidase that works synergistically with chitinases. NAGK is a key enzyme for the generation of UDP-Nacetylglucosamine (UDP-GlcNAc) and for the conversion of GlcNAc into GlcNAc 6-phosphate (GlcNAc-6-P). In this study, NAG and NAGK genes were identified from Holotrichia parallela, a polyphagous soil pest that causes serious damage to crops. The spatiotemporal expression investigated by RT-qPCR indicated that the two genes are expressed in all larval developmental stages. HpNAG is highly expressed in the integument and HpNAGK overexpressed in the midgut. After injection of dsHpNAG and dsHpNAGK, a significant RNAi effect was found after 72 h and larvae stopped growing. The survival rates of larvae were 13.3% and 16.7%, respectively. RNAi of HpNAG and HpNAGK regulated the expression levels of chitin metabolism-related genes, indicating that these two genes could be critical in the chitin metabolism. Furthermore, silencing HpNAG and HpNAGK reduced the thickness of the cuticle, and decreased its content of chitin. The study will lay a foundation for further clarifying the mechanism of chitin metabolism and provide potential targets for the biological control of H. parallela larvae.

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