4.6 Article

Transcriptional Dynamics Induced by Diapause Hormone in the Silkworm, Bombyx mori

Journal

BIOLOGY-BASEL
Volume 11, Issue 9, Pages -

Publisher

MDPI
DOI: 10.3390/biology11091313

Keywords

silkworm; diapause; diapause hormone; RNA sequencing

Categories

Funding

  1. National Natural Science Foundation of China [32000336, 32000339]

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This study investigates the expression pattern of diapause hormone (DH) receptor in silkworm pupae and analyzes gene expression profile in the ovaries after DH injection. The results show that differentially expressed genes related to hormone signaling, cellular detoxification, ribosomal proteins, lipid metabolism, and epigenetic modifications are identified. The study provides valuable insights into gene expression variation during the early phase of DH release in silkworm.
Simple Summary Most insects species enter a diapause period to ensure their survival under unsuitable environments. In the silkworm, Bombyx mori, diapause occurs at the embryonic stage and is regulated by the diapause hormone (DH). Here, we directly injected DH into the female pupae and investigated the DH receptor expression pattern. Using RNA sequencing, we analyzed the gene expression profile in the developing ovaries after the injection of DH. Diapause is a form of dormancy that organisms use to adapt to extreme environments by exhibiting developmental arrest. In the silkworm, Bombyx mori, diapause is thought to be elicited by diapause hormone (DH) signaling, which consists of interactions between DH and the DH receptor (DHR). However, the steps downstream of the DH signaling pathway are largely unknown. In the present study, we directly injected synthesized DH into the female pupae of a multivoltine, non-diapausing strain at 36 h after pupation. We found that the mRNA level of DHR declined at 4 h and recovered at 12 h after the injection of DH. Thus, we sequenced the transcriptome of the ovaries at 4 h and 12 h after the injection of DH. We identified 60 and 221 differentially expressed genes at 4 h and 12 h after the injection, respectively. All DEGs were identified, relating to 20E-related genes, JH-related genes, cellular detoxification, ribosomal proteins, lipid metabolism, and epigenetic modifications. Eleven genes were selected from the above categories to verify the transcriptome data. The qRT-PCR and RNA-Seq expression patterns of the genes were consistent, which indicated the authenticity and reliability of the transcriptome data. This study dramatically expands upon our knowledge of gene expression variation at the early phase of DH release.

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