@article{49057fc1947f4163be69c1a9ba892c12,
title = "A transposon-introduced G-quadruplex motif is selectively retained and constrained to downregulate CYP321A1",
abstract = "Insects utilize xenobiotic compounds to up- and downregulate cytochrome P450 monooxygenases (P450s) involved in detoxification of toxic xenobiotics including phytochemicals and pesticides. G-quadruplexes (G4)-forming DNA motifs are enriched in the promoter regions of transcription factors and function as cis-acting elements to regulate these genes. Whether and how P450s gain and keep G4 DNA motifs to regulate their expression still remain unexplored. Here, we show that CYP321A1, a xenobiotic-metabolizing P450 from Helicoverpa zea, a polyphagous insect of economic importance, has acquired and preserved a G4 DNA motif by selectively retaining a transposon known as HzIS1-3 that carries this G4 DNA motif in its promoter region. The HzIS1-3 G4 DNA motif acts as a silencer to suppress the constitutive and induced expression of CYP321A1 by plant allelochemicals flavone and xanthotoxin through folding into an intramolecular parallel or hybrid-1 conformation in the absence or presence of K+. The G4 ligand N-methylmesoporphyrin IX (NMM) strengthens the silencing effect of HzIS1-3 G4 DNA motif by switching its structure from hybrid-1 to hybrid-2. The enrichment of transposons in P450s and other environment-adaptation genes implies that selective retention of G4 DNA motif-carrying transposons may be the main evolutionary route for these genes to obtain G4 DNA motifs.",
keywords = "DNA secondary structure, Helicoverpa zea, gene regulation, natural selection, plant allelochemicals, signaling pathway, silencer",
author = "Zhongyuan Deng and Yuting Zhang and Chao Gao and Wei Shen and Shan Wang and Xinzhi Ni and Sisi Liu and Xianchun Li",
note = "Funding Information: We acknowledge the research group of Prof. Xiang Zhou (College of Chemistry and Molecular Science, Key laboratory of Biomedical Polymers of Ministry of Education, Wuhan University) for providing the Chirascan CD spectrophotometer. We thank Dr. Chunni Zhang for making the wildtype CYP321A1-pGL3 construct and Dr. Cynthia L. Goodman for providing the H. zea fat body cell line. This work was supported by the National Natural Science Foundation of China (No. 31701791); National Science Foundation of China (NSFC)-Henan Joint major grant (No. U2004206); the State Key Laboratory of Cotton Biology (No. CB2020A06); and the USDA National Institute of Food and Agriculture Hatch Project (No. ARZT-1370680-R31-R31-172). The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication. Funding Information: We acknowledge the research group of Prof. Xiang Zhou (College of Chemistry and Molecular Science, Key laboratory of Biomedical Polymers of Ministry of Education, Wuhan University) for providing the Chirascan CD spectrophotometer. We thank Dr. Chunni Zhang for making the wildtype CYP321A1‐pGL3 construct and Dr. Cynthia L. Goodman for providing the fat body cell line. This work was supported by the National Natural Science Foundation of China (No. 31701791); National Science Foundation of China (NSFC)‐Henan Joint major grant (No. U2004206); the State Key Laboratory of Cotton Biology (No. CB2020A06); and the USDA National Institute of Food and Agriculture Hatch Project (No. ARZT‐1370680‐R31‐R31‐172). The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication. H. zea Publisher Copyright: {\textcopyright} 2022 Institute of Zoology, Chinese Academy of Sciences.",
year = "2022",
month = dec,
doi = "10.1111/1744-7917.13021",
language = "English (US)",
volume = "29",
pages = "1629--1642",
journal = "Insect Science",
issn = "1672-9609",
publisher = "Wiley-Blackwell",
number = "6",
}