4.6 Article

Gene expression of ribosomal protein mRNA in Chironomus riparius: Effects of endocrine disruptor chemicals and antibiotics

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.cbpc.2012.05.002

关键词

Aquatic invertebrate; Ribosomal genes; Ribosomal protein S3; Ribosomal protein S6; Di(2-ethylhexyl) phthalate (DEHP); Bisphenol A (BPA); 4-Nonylphenol (4NP); Fenbendazole; Sulfathiazole; Lincomycin

资金

  1. National Research Foundation of Korea Grant
  2. Korean Government [NRF-2012-0004186, NRF-2012-0004352]
  3. National Research Foundation of Korea [2011-0007657] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Ribosomal protein genes are essential for cellular development. To examine the effects of ribosomal protein genes under various cellular stress conditions in chironomids, ribosomal protein S3 (RpS3) and S6 (RpS6) cDNA from Chironomus riparius were characterized and their expression was analyzed during development. A comparative and phylogenetic study among different orders of insects was carried out by analysis of sequence databases. C. riparius RpS3 was highly conserved at the protein level and shared over 85% amino acid identity with homologous sequences from other insects. RpS6 also showed approximately 80% amino acid identity. The RpS3 and S6 transcripts were present during different developmental stages but were most abundant during the embryonic stage. Furthermore, expression of the previously reported ribosomal proteins RpL11, L13, and L15, as well as RpS3 and S6 was analyzed following exposure to various concentrations of three endocrine disruptor chemicals (EDCs), di(2-ethylhexyl) phthalate, bisphenol A, and 4-nonylphenol (4NP), and the veterinary antibiotics (VAs) fenbendazole, sulfathiazole, and lincomycin. Only RpS3 gene expression was up-regulated significantly in response to EDCs and fenbendazole. However, the C. riparius ribosomal proteins showed a limited response to cellular stress, following exposure to EDCs and VAs. (c) 2012 Elsevier Inc. All rights reserved.

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