| Literature DB >> 21678487 |
Hua-Jun Yang1, Mei-Xian Wang, Peng Zhang, Awquib Sabhat, Firdose Ahmad Malik, Roy Bhaskar, Fang Zhou, Xing-Hua Li, Jia-Biao Hu, Chun-Guang Sun, Yan-Shan Niu, Yun-Gen Miao.
Abstract
The physiological titer of molting hormones in insects depends on relative activities of synthesis and degradation pathways. Ecdysone oxidase (EO) is a key enzyme in the inactivation of ecdysteroid. However, there are only a few reports on ecdysteroid inactivation and its enzymes in silkworm. In this study, we cloned and characterized the Bombyx mori EO (BmEO). The BmEO cDNA contains an ORF of 1,695 bp and the deduced protein sequence contains 564 amino acid residues. The deduced protein sequence contains two functional domains of glucose-methanol-choline oxidoreductase in N-terminal and C-terminal. Comparing the expression levels of BmEO in different tissues, high transcription was mainly present in hemocytes. Reduced expression of this enzyme is expected to lead to pathological accumulation of ecdysone in the hemolymph of silkworm larvae or pupae. Our data show that RNA inference of BmEO transcripts resulted in the accumulation of ecdysteroid and death of larvae or pupae. We infer that EO is a crucial element in the physiology of insect development.Entities:
Keywords: Bombyx mori; ecdysone oxidase; ecdysteroids; molting hormones
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Year: 2011 PMID: 21678487 DOI: 10.1002/arch.20436
Source DB: PubMed Journal: Arch Insect Biochem Physiol ISSN: 0739-4462 Impact factor: 1.698