MicroRNA let-7 targets BmCDK1 to regulate cell proliferation and endomitosis of silk gland in the silkworm,Bombyx mori  

作　　者：Wei Wang Linshengzhe Ji Xinyuan Jing Ping Zhao Qingyou Xia 

机构地区：[1]Integrative Science Center of Germplasm Creation in Western China(Chongqing)Science City,Biological Science Research Center,Southwest University,China [2]Key Laboratory for Germplasm Creation in Upper Reaches of the Yangtze River,Ministry of Agriculture and Rural Affairs,Chongqing,China [3]Engineering Laboratory of Sericultural and Functional Genome and Biotechnology,Development and Reform Commission,Chongqing,China

出　　处：《Insect Science》2024年第4期1026-1040,共15页昆虫科学（英文版）

基　　金：supported by grants from the National Natural Science Foundation of China(No.32102614);the National Key Research and Development Program of China(No.2022YFD1201600);the Natural Science Foundation of Chongqing,China(No.cstc2021jcyj-bsh0151);the Chongqing Special Support fund for Post Doctor(No.2010010006115189).

摘　　要：MicroRNAs play critical roles in multiple developmental processes in insects.Our previous study showed that CRISPR/Cas9-mediated knock down of the microRNA let-7 in silkworms increased the size of larvae and silk glands,thereby improving the silk production capacity.In this study,we elucidate the molecular mechanism underlying of let-7 regulates growth.Identification of differentially expressed genes in response to let-7 knock down revealed enrichment of pathways associated with cell proliferation and DNA replication.let-7 dysregulation affected the cell cycle and proliferation of the Bombyx mori cell line BmN.Dual-luciferase and target site mutation assays showed that BmCDK1 is a direct target gene of let-7,with only 1 binding site on its 3′-untranslated region.RNA interference of BmCDK1 inhibited cell proliferation,but this effect was counteracted by co-transfection with let-7 antagomir.Moreover,let-7 knock down induced BmCDK1 expression and promoted cell proliferation in multiple tissues,and further induced endomitosis in the silk gland in vivo.Knock down of BmCDK1 resulted in abnormal formation of a new epidermis,and larval development was arrested at the 2nd or 3rd molt stage.Taken together,our results demonstrated that BmCDK1 is a novel target of let-7 in cell fate determination,possessing potential for improving silk yield in silkworm.

关 键 词：BmCDKI CRISPR/Cas9 cell proliferation LET-7 SILKWORM 

分 类 号：Q96[生物学—昆虫学]