Ovarian transcriptome analyses indicate that weak juvenile hormone signaling underlies the molecular basis of oogenesis deficiencies in mosquitoes

. 2025 Jun 09 ; 23 (1) : 160. [epub] 20250609

Jazyk angličtina Země Anglie, Velká Británie Médium electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid40484957

Grantová podpora
R21 AI167849 NIAID NIH HHS - United States
22-21244S Grantová Agentura České Republiky
CZ.02.1.01/0.0/0.0/16_019/0000759 Centre for Research of Pathogenicity and Virulence of Parasite
R21AI167849 National Institutes of Health-NIAID

Odkazy

PubMed 40484957
PubMed Central PMC12147312
DOI 10.1186/s12915-025-02266-z
PII: 10.1186/s12915-025-02266-z
Knihovny.cz E-zdroje

BACKGROUND: Juvenile hormone (JH) is synthesized by the corpora allata (CA) and controls development and reproduction in insects. We recently used CRISPR/Cas9 to establish a line lacking the enzyme that catalyzes the final step of JH biosynthesis in mosquitoes, a P450 epoxidase. The CA of the epox-/- mutants do not synthesize epoxidized JH III but methyl farneosate (MF), a weak agonist of the JH receptor. Female epox-/- mosquitoes have reduced JH signaling and show a substantial loss of reproductive fitness. To understand the molecular basis of this loss of fitness, we constructed ovarian mRNA libraries of Ae. aegypti of the Orlando strain wild-type (WT) and epoxidase null mutants (epox-/-) and investigated differential expression of reproductive genes. RESULTS: We performed triplicate RNA-seq analyses of female WT and epox-/- ovaries dissected at four critical stages of oogenesis: Ovaries from newly eclosed females (0h), sugar-fed females at 4 days post-eclosion (4d SF), females 16h (16h BF), and 48 h after a blood meal (48h BF). Silencing of epoxidase resulted in a drastic change in the expression of thousands of genes. CONCLUSIONS: Our results suggest that epoxidase deficiency leads to a reduction in JH signaling that has significant effects on Ae. aegypti ovarian transcriptome profiles. Ecdysteroid titers are dysregulated in the mutants, leading to a significant delay in the expression of vitelline membrane genes and other transcripts. We discovered changes in the expression of 230 long non-coding RNAs (lncRNAs) that may play an important role in the regulation of ovarian genes.

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