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Heat shock protein 83 (hsp83) facilitates methoprenetolerant (met) nuclear import to modulate juvenile hormone signaling

  • Qianyu He*
  • , Di Wen
  • , Qiangqiang Jia
  • , Chunlai Cui
  • , Jian Wang
  • , Subba R. Pallii
  • , Sheng Li
  • *Corresponding author for this work
  • CAS - Center for Excellence in Molecular Plant Sciences
  • Heilongjiang Bayi Agricultural University
  • University of Maryland, College Park
  • University of Kentucky

Research output: Contribution to journalArticlepeer-review

Abstract

Juvenile hormone (JH) receptors, methoprene-tolerant (Met) and Germ-cell expressed (Gee), transduce JH signals to induce Kr-hl expression in Drosophila. Dual luciferase assay identified a 120-bp JH response region (JHRR) in the Kr-h1α promoter. Both in vitro and in vivo experiments revealed that Met and Gee transduce JH signals to induce Kr-hl expression through the JHRR. DNA affinity purification identified chaperone protein Hsp83 as one of the proteins bound to the JHRR in the presence of JH. Interestingly, Hsp83 physically interacts with PAS-B and basic helix-loop-helix domains of Met, and JH induces MetHsp83 interaction. As determined by immunohistochemistry, Met is mainly distributed in the cytoplasm of fat body cells of the larval when the JH titer is low and JH induces Met nuclear import. Hsp83 was accumulated in the cytoplasm area adjunct to the nucleus in the presence of JH and Met/Gce. Loss-of-function of Hsp83 attenuated JH binding and JH-induced nuclear import of Met, resulting in a decrease in the JHRR-driven reporter activity leading to reduction of Kr-hl expression. These data show that Hsp83 facilitates the JH-induced nuclear import of Met that induces Kr-hl expression through the JHRR.

Original languageEnglish
Pages (from-to)27874-27885
Number of pages12
JournalJournal of Biological Chemistry
Volume289
Issue number40
DOIs
StatePublished - 3 Oct 2014
Externally publishedYes

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