Abstract

Three distinct classes of nuclear receptors, EcR, E75, and HR3, are key regulators in the ecdysone-inducible gene activation cascade in insects. The transcription of these genes is induced by ecdysone (20E) differently, although the detailed mechanisms underlying their responses to 20E are largely unknown. We identified ecdysone response elements (EcREs) present in the promoters of genes coding BmEcR-B1, BmE75-A, and BHR3-B isoforms from Bombyx mori employing luciferase reporter assays in an ecdysteroid-responsive cultured cell line, NIAS-Bm-aff3 (aff3). The EcRE of BmEcR-B1 at −2800 comprises of two adjacent elements separated by 5 bp, E1 (15 bp) and E2 (21 bp), both of which are required for the 20E response. Further analysis using electrophoretic mobility shift assays showed that E1 binds to the EcR/USP heterodimer and that E2 may bind to the E-box (CACGTG) binding factor such as bHLH protein. The unique E1+E2-type EcRE is also detected in the promoter upstream regions of EcR-B1 from seven lepidopteran species studied. In contrast, both a 20 bp EcRE identified in the promoter of BmE75-A and a 18 bp EcRE identified in the BHR3-B promoter, contained only E1-type EcR/USP binding element but the E2 type element was not in the promoter regions of these genes. The combination of presence of the E2 element or other cis-regulatory elements in promoter regions explains the different 20E response of each class of nuclear receptor genes. Furthermore, the E1+E2 structure for EcR-B1 can be involved in a possible cross-talk between ecdysteroid and other regulatory pathways.

Highlights

  • The steroid hormone ecdysteroid, primarily 20-hydroxyecdysone (20E), coordinates various developmental and physiological processes in insects [1]

  • Genomic structures of BmEcR, BmE75 and BHR3 Based on the silkworm genome sequence (Scaffold version 2.3), BmEcR is mapped on linkage group 10 and its entire region is included in one scaffold, Bm_scaf10

  • We compared the reporter activity of a swapped construct with an original plasmid at various concentration of 20E in the aff3 cell (Fig. S5B). We found that their dose response to 20E was basically same between the original and the swapped construct, both for BmE75A and BHR3-B, indicating that BmE75-A ecdysone response elements (EcREs) and BHR3-B EcRE have the same effect on the dose response to 20E and that some other cis-regulatory elements are involved in their different response to 20E

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Summary

Introduction

The steroid hormone ecdysteroid, primarily 20-hydroxyecdysone (20E), coordinates various developmental and physiological processes in insects [1]. Ecdysone receptor (EcR) and ultraspiracle (USP) form heterodimer complex that binds to 20E and regulates the expression of target genes in stage- and tissue-specific manners [4,6,7]. The alternative expression of EcR isoforms is reported to correlate with the cellular fate of several tissues in holometabolous insects [9,10,11,12], and thought to be a key step in regulating morphogenesis and tissue differentiation during metamorphosis. Other members of nuclear receptors, E75 and hormone receptor 3 (HR3), a vertebrate RORa homologue in insects, are known to have several isoforms that differ in structure in the N terminus and to be key regulators in the ecdysone-inducible gene activation cascade [3,4]

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