Drosophila transcription factor NF-Y suppresses transcription of the lipase 4 gene, a key gene for lipid storage

Exp Cell Res. 2022 Nov 1;420(1):113307. doi: 10.1016/j.yexcr.2022.113307. Epub 2022 Aug 24.

Abstract

The CCAAT motif-binding factor NF-Y consists of three different subunits, NF-YA, NF-YB, and NF-YC. Although it is suggested that NF-Y activity is essential for normal tissue homeostasis, survival, and metabolic function, its precise role in lipid metabolism is not clarified yet. In Drosophila, eye disc specific knockdown of Drosophila NF-YA (dNF-YA) induced aberrant morphology of the compound eye, the rough eye phenotype in adults and mutation of the lipase 4 (lip4) gene suppressed the rough eye phenotype. RNA-seq analyses with dNF-YA knockdown third instar larvae identified the lip4 gene as one of the genes that are up-regulated by the dNF-YA knockdown. We identified three dNF-Y-binding consensuses in the 5'flanking region of the lip4 gene, and a chromatin immunoprecipitation assay with the specific anti-dNF-YA IgG demonstrated dNF-Y binding to this genomic region. The luciferase transient expression assay with cultured Drosophila S2 cells and the lip4 promoter-luciferase fusion genes with and without mutations in the dNF-Y-binding consensuses showed that each of the three dNF-Y consensus sequences negatively regulated lip4 gene promoter activity. Consistent with these results, qRT-PCR analysis with the dNF-YA knockdown third instar larvae revealed that endogenous lip4 mRNA levels were increased by the knockdown of dNF-YA in vivo. The specific knockdown of dNF-YA in the fat body with the collagen-GAL4 driver resulted in smaller oil droplets in the fat body cells. Collectively, these results suggest that dNF-Y is involved in lipid storage through its negative regulation of lip4 gene transcription.

Keywords: Drosophila; Fat body; Lipase 4; Lipid storage; NF-Y.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CCAAT-Binding Factor / genetics
  • CCAAT-Binding Factor / metabolism
  • Drosophila* / metabolism
  • Genes, vif
  • Immunoglobulin G / metabolism
  • Lipase / genetics
  • Lipase / metabolism
  • Lipids
  • Luciferases / metabolism
  • RNA, Messenger / metabolism
  • Transcription Factors* / metabolism

Substances

  • CCAAT-Binding Factor
  • Immunoglobulin G
  • Lipids
  • RNA, Messenger
  • Transcription Factors
  • Luciferases
  • Lipase