Van Loy Tom, Van Hiel Matthias B, Vandersmissen Hans Peter, Poels Jeroen, Mendive Fernando, Vassart Gilbert, Vanden Broeck Jozef
Animal Physiology and Neurobiology, Laboratory for Developmental Physiology, Genomics and Proteomics, Zoological Institute, K.U.Leuven, Naamsestraat 59, B-3000, Belgium.
Gen Comp Endocrinol. 2007 Aug-Sep;153(1-3):59-63. doi: 10.1016/j.ygcen.2006.12.004. Epub 2006 Dec 27.
Bursicon bioactivity is essential for tanning of the exoskeleton and for wing spreading behavior that occur in newly emerged adult insects. Previously, we demonstrated that in the fruit fly, Drosophila melanogaster, bursicon exists as a heterodimeric cystine knot protein that activates the leucine-rich repeats containing G protein-coupled receptor 2 (DLGR2). By performing similarity based in silico searches in genomic and complementary DNA databases, we identified bursicon homologous sequences in several protostomian as well as deuterostomian invertebrates. In the genome of the honeybee, Apis mellifera, the coding regions for bursicon cystine knot subunits are organized in a genomic locus of approximately 4 kilobase pairs. Reverse transcription PCR analysis indicates that this region likely codes for two distinct bursicon cystine knot subunits. Our results illustrate the remarkable conservation of bursicon in invertebrate species and provide an avenue for functional analyses of this hormone in a wide range of animal species.
羽化激素的生物活性对于新羽化的成年昆虫的外骨骼鞣化和展翅行为至关重要。此前,我们证明在果蝇(Drosophila melanogaster)中,羽化激素以异源二聚体胱氨酸结蛋白的形式存在,它可激活含亮氨酸丰富重复序列的G蛋白偶联受体2(DLGR2)。通过在基因组和互补DNA数据库中进行基于相似性的电子搜索,我们在几种原口动物以及后口动物无脊椎动物中鉴定出了羽化激素同源序列。在蜜蜂(Apis mellifera)的基因组中,羽化激素胱氨酸结亚基的编码区位于一个约4千碱基对的基因组位点上。逆转录PCR分析表明,该区域可能编码两种不同的羽化激素胱氨酸结亚基。我们的结果说明了羽化激素在无脊椎动物物种中的显著保守性,并为在广泛的动物物种中对这种激素进行功能分析提供了一条途径。