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剪接因子Nova调控了二化螟(鳞翅目:草螟科)γ-氨基丁酸受体亚基RDL第3和第6外显子中的剪接变体。

Splicing factor Nova regulates the splice variants in exons 3 and 6 of GABA receptor subunit RDL from Chilo suppressalis Walker (Lepidoptera: Crambidae).

作者信息

Song Zijiao, Jiang Jie, Tang Tao, Luo Guanghua, Wang Junyan, Lin Kaixiang, Mu Lili, Zhao Chunqing

机构信息

State Key Laboratory of Agricultural and Forestry Biosecurity, College of Plant Protection, Nanjing Agricultural University, Nanjing 211800, PR China.

Institute of Plant Protection, Hunan Academy of Agricultural Sciences, Changsha 410125, PR China.

出版信息

Pestic Biochem Physiol. 2025 Nov;214:106556. doi: 10.1016/j.pestbp.2025.106556. Epub 2025 Jul 8.

Abstract

The insect ionotropic γ-aminobutyric acid (GABA) receptor is an important insecticide target, and alternative splicing (AS) among exons 3a, 3b, 6a, and 6b of its RDL subunit is ubiquitous in insects; however, the AS factors and mechanisms remain unclear. While the neuro-oncological ventral antigen (Nova) is known to regulate AS of the γ2 subunit of mammalian GABA receptors, its role in insects remains unexplored. Two CsNova isoforms, CsNova-X1 and CsNova-X3, were identified by BLAST in the third-generation transcriptome of Chilo suppressalis. These isoforms exhibited conserved KH domains with the open reading frames of CsNova-X1 and CsNova-X3 measuring 1638 bp and 1572 bp, respectively. Compared with CsNova-X1, CsNova-X3 lacks 22 amino acid residues in the N-terminal region. Developmental expression profiling revealed peak mRNA levels during the pupal stage. RNA interference (RNAi)-mediated knockdown of CsNova significantly reduced CsRDL-3a/3b/6a transcript levels after 72 h. Molecular docking simulations revealed that the UCAUCAC motif in the downstream of exon 2 of CsRDL could interact with CsNova-X1, while the UCAU and UCAC motifs in exon 6b and its flanking regions could interact with CsNova-X3. In conclusion, Nova was cloned from the Lepidoptera insect for the first time and could regulate the AS process of exon 3 and exon 6 of CsRDL, laying a foundation for in-depth studies on the regulatory mechanism of AS for RDL and the development of RNAi-based pesticides targeting these interactions.

摘要

昆虫离子型γ-氨基丁酸(GABA)受体是一种重要的杀虫剂作用靶标,其RDL亚基外显子3a、3b、6a和6b之间的可变剪接(AS)在昆虫中普遍存在;然而,可变剪接的因子和机制仍不清楚。虽然已知神经肿瘤腹侧抗原(Nova)可调节哺乳动物GABA受体γ2亚基的可变剪接,但其在昆虫中的作用尚未得到探索。通过在二化螟的第三代转录组中进行BLAST分析,鉴定出了两种CsNova亚型,即CsNova-X1和CsNova-X3。这些亚型具有保守的KH结构域,CsNova-X1和CsNova-X3的开放阅读框分别为1638 bp和1572 bp。与CsNova-X1相比,CsNova-X3在N端区域缺少22个氨基酸残基。发育表达谱分析显示,蛹期mRNA水平达到峰值。RNA干扰(RNAi)介导的CsNova敲低在72小时后显著降低了CsRDL-3a/3b/6a的转录水平。分子对接模拟显示,CsRDL外显子2下游的UCAUCAC基序可与CsNova-X1相互作用,而外显子6b及其侧翼区域的UCAU和UCAC基序可与CsNova-X3相互作用。总之,首次从鳞翅目昆虫中克隆出Nova,其可调节CsRDL外显子3和外显子6的可变剪接过程,为深入研究RDL可变剪接调控机制以及开发针对这些相互作用的基于RNAi的杀虫剂奠定了基础。

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