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Priming effect in gene activation by juvenile hormone in locust fat body
Author(s) -
Wyatt G.R.,
Braun R.P.,
Zhang J.
Publication year - 1996
Publication title -
archives of insect biochemistry and physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.576
H-Index - 66
eISSN - 1520-6327
pISSN - 0739-4462
DOI - 10.1002/(sici)1520-6327(1996)32:3/4<633::aid-arch34>3.0.co;2-b
Subject(s) - juvenile hormone , methoprene , biology , pyriproxyfen , promoter , locust , transcription factor , transcription (linguistics) , vitellogenin , migratory locust , gene , endocrinology , medicine , priming (agriculture) , hemolymph , gene expression , microbiology and biotechnology , hormone , biochemistry , botany , linguistics , philosophy , germination , larva
When an active JH analog (methoprene or pyriproxyfen) is administered to JH‐deprived (precocene‐treated) adult female locusts, there is a delay of about 24 h before vitellogenin (Vg), the product of a JH‐dependent gene, is found in the hemolymph. If a dose of JH III or methoprene, itself too low to induce any detectable Vg, is administered 12–48 h before the inducing dose of JH analog, however, the appearance of Vg after the inducing treatment is accelerated by about 12 h. This effect is described as priming. It is proposed that priming involves the synthesis of a specific transcription factor for Vg and other JH‐dependent genes. A system suitable for testing this hypothesis is provided by transcription in locust fat body nuclear extracts, using G‐free cassettes as reporter sequences. Protein extracted from fat body of JH‐deficient (precocene‐treated) locusts transcribes from the control non‐specific AdML promoter but not from the promoters of the two JH target genes. Preparations from normal adult female fat body, or from that of locusts treated with precocene and later with a JH analog, on the other hand, transcribe from the promoters of the JH‐dependent Vg and jhp21 genes, as well as the AdML promoter. This demonstrates the JH‐induced appearance of a specific transcription factor. The cell‐free transcription system is suitable for further analysis of the molecular components of JH regulated transcription. © 1996 Wiley‐Liss, Inc.

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