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Single-cell transcriptomics of the Drosophila ring gland identifies the SoxN–Vvl complex as a key regulator of juvenile hormone biosynthesis

  • Yuhan Luo
  • , Nan Chen
  • , Yue Gao
  • , Wei Luo
  • , Shanshan Liu
  • , Yang Li
  • , Hanyue Wang
  • , Xiangbin Gao
  • , Jiawei Chen
  • , Haosheng Ye
  • , Kirst King-Jones
  • , Subba Reddy Palli
  • , Sheng Li
  • , Suning Liu

Producción científica: Articlerevisión exhaustiva

Resumen

Juvenile hormone (JH) is essential for maintaining juvenile status and promoting reproduction in insects, yet the transcriptional regulation of JH biosynthesis remains poorly understood. Previous transcriptomic studies of the Drosophila ring gland—which is composed of the corpus allatum (CA), prothoracic gland (PG), and corpora cardiaca (CC)—have treated the ring gland as a single tissue. As a result, these approaches lacked the resolution necessary to dissect JH biosynthesis and its regulation in a cell-type-specific manner. To overcome this limitation, we performed single-cell RNA sequencing (scRNA-seq) of 7,919 cells isolated from the larval ring glands. This analysis resolved distinct transcriptional profiles for the CA, PG, and CC, and enabled the identification of CA-specific transcription factors. Among them, SoxNeuro (SoxN), was found to be essential for JH biosynthesis and functionally important for both metamorphosis and reproduction. We further demonstrate that SoxN physically interacts with Ventral veins lacking (Vvl) to form a transcriptional complex that directly regulates Jhamt, a rate-limiting enzyme in JH biosynthesis, via a defined promoter region. Together, this work presents a single-cell transcriptomic atlas of the Drosophila ring gland and identifies the SoxN–Vvl complex as a critical regulator of JH biosynthesis, offering insight into the transcriptional control of insect endocrine function.

Idioma originalEnglish
Número de artículoe2520504123
PublicaciónProceedings of the National Academy of Sciences of the United States of America
Volumen123
N.º6
DOI
EstadoPublished - feb 2026

Nota bibliográfica

Publisher Copyright:
Copyright © 2026 the Author(s).

Financiación

ACKNOWLEDGMENTS. We thank the Bloomington Drosophila Stock Center, the Tsinghua Fly Center, the Vienna Drosophila Resource Center, and the Core Facility of Drosophila Resource and Technology (CEMCS, CAS) for providing fly stocks. We are grateful to Dr. Zizhang Zhou for providing the tub-EGFP vector and to the Core Facility of Drosophila Resource and Technology (CEMCS, CAS) and Qidong Fungene Biotechnology for generating transgenic flies. We thank Dr. Ryusuke Niwa for helpful comments on this manuscript. This work was supported by the National Natural Science Foundation of China (Grant No. 32222013 to Suning Liu, 32220103003 to S. Li, 32370511 to N.C., and 32100375 to W.L.), the Guangdong Natural Science Funds for Distinguished Young Scholar (2022B1515020043 to Suning Liu), Natural Science Foundation in Guangdong Province (2023A1515010409 to W.L.) and Science and Technology Projects in Guangzhou (2025A04J5446 to Suning Liu, 2025A04J0466 to N.C.).

FinanciadoresNúmero del financiador
Natural Science Foundation of Guangdong Province2023A1515010409
Guangzhou Municipal Science and Technology Program key projects2025A04J5446, 2025A04J0466
National Natural Science Foundation of China (NSFC)32370511, 32222013, 32100375, 32220103003
Science Fund for Distinguished Young Scholars of Guangdong Province2022B1515020043

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