期刊文献+

Molecular characterization and m RNA expression of ribosomal protein L8 in Rana nigromaculata during development and under exposure to hormones 被引量:6

Molecular characterization and m RNA expression of ribosomal protein L8 in Rana nigromaculata during development and under exposure to hormones
原文传递
导出
摘要 Like Xenopus laeuis, some species of the Rang genus are also used to study endocrine disrupting chemicals (EDCs). Although ribosomal protein L8 (rp18) is the most-used reference gene for analyzing gene expression by quantitative reverse transcription polymerase chain reaction in Rang, its suitability as the reference gene has never been validated in any species of the Rana genus. We characterized rp18 cDNA in Rana nigromaculata, a promising native species in East Asia for assaying endocrine disrupting effects. We found that the rp18 cDNA consisted of 919 bp and encoded 257 amino acids, exhibiting high identities of amino acid sequence with known rp18 in other Rana species. Then, we examined the stability of mRNA expression during development. Compared with elongation factor 1 alpha 1, another common housekeeping gene, neither stage-specific nor tissue-specific expression of the rp18 gene was found in all tissues examined (brain, liver, intestine, tail, testis and ovary) during R. nigromaculata development. Finally, we investigated rp18 expression under exposure to hormones. No change in rp18 mRNA expression was found under exposure to thyroid hormone (T4) and estrogen (estradiol), whereas expression of the corresponding biomarker genes was induced. Our results show that rp18 is an appropriate reference gene for analyzing gene expression by quantitative reverse transcription polymerase chain reaction for assaying EDCs using R. nigromaculata, and might also provide support for using rp18 as a reference gene in other Rang species due to the high conservation of rp18 among the Rana genus. Like Xenopus laeuis, some species of the Rang genus are also used to study endocrine disrupting chemicals (EDCs). Although ribosomal protein L8 (rp18) is the most-used reference gene for analyzing gene expression by quantitative reverse transcription polymerase chain reaction in Rang, its suitability as the reference gene has never been validated in any species of the Rana genus. We characterized rp18 cDNA in Rana nigromaculata, a promising native species in East Asia for assaying endocrine disrupting effects. We found that the rp18 cDNA consisted of 919 bp and encoded 257 amino acids, exhibiting high identities of amino acid sequence with known rp18 in other Rana species. Then, we examined the stability of mRNA expression during development. Compared with elongation factor 1 alpha 1, another common housekeeping gene, neither stage-specific nor tissue-specific expression of the rp18 gene was found in all tissues examined (brain, liver, intestine, tail, testis and ovary) during R. nigromaculata development. Finally, we investigated rp18 expression under exposure to hormones. No change in rp18 mRNA expression was found under exposure to thyroid hormone (T4) and estrogen (estradiol), whereas expression of the corresponding biomarker genes was induced. Our results show that rp18 is an appropriate reference gene for analyzing gene expression by quantitative reverse transcription polymerase chain reaction for assaying EDCs using R. nigromaculata, and might also provide support for using rp18 as a reference gene in other Rang species due to the high conservation of rp18 among the Rana genus.
出处 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2014年第11期2331-2339,共9页 环境科学学报(英文版)
基金 supported by the National High Technology Research and Development Program (863) of China (No. 2012AA06A302) the Public Welfare Research Project for Environmental Protection (No. 201109048) the National Natural Science Foundation of China (No. 21077125)
关键词 Ribosomal protein L8 Rana nigromaculata Endocrine disrupting chemical Quantitative RT-PCR Reference gene Ribosomal protein L8 Rana nigromaculata Endocrine disrupting chemical Quantitative RT-PCR Reference gene
  • 相关文献

参考文献41

  • 1Arukwe, A., 2006. Toxicological housekeeping genes: do they really keep the house? Environ. Sci. Technol. 40 (24), 7944-7949.
  • 2Berg, C., Gyllenhammar, I., Kvarnryd, M., 2009. Xenopus tropicalis as a test system for developmental and reproductive toxicity. J. Toxicol. Environ. Health A 72 (3^), 219-225.
  • 3Burggren, W.W., Warburton, S., 2007. Amphibians as animal models for laboratory research in physiology. ILAR J. 48 (3), 260-269.
  • 4Bustin, S.A., Nolan, T., 2004. Pitfalls of quantitative real-time reverse-transcription polymerase chain reaction. J. Biomol. Tech. 15 (3), 155-166.
  • 5Croteau, M.C., Davidson, M., Duarte-Guterman, P., Wade, M., Popesku, J.T., Wiens, S., et al., 2009. Assessment of thyroid system disruption in Rana pipiens tadpoles chronically exposed to UVB radiation and 4-tert-octylphenol. Aquat. Toxicol. 95 (2), 81-92.
  • 6Degitz, S.J., Holcombe, G.W., Flynn, K.M., Kosian, P.A., Korte, J.J., Tietge, J.E., 2005. Progress towards development of an amphibian-based thyroid screening assay using Xenopus laeuis. Organismal and thyroidal responses to the model compounds.
  • 76-propylthiouracil, methimazole, and thyroxine. Toxicol. Sci. 87 (2), 353-364.
  • 8Dhorne-Pollet, S., Thelie, A., Pollet, N., 2013. Validation of novel reference genes for RT-qPCR studies of gene expression in Xenopus tropicalis during embryonic and post-embryonic development. Dev. Dyn. 242 (6), 709-717.
  • 9Filby, A.L., Tyler, C.R., 2007. Appropriate ‘housekeeping’ genes for use in expression profiling the effects of environmental estrogens in fish. BMC Mol. Biol. 8, 10.
  • 10Fini, J.B., Le Mevel, S., Palmier, K., Danas, V.M., Punzon, I., Richardson, S.J., et al., 2012. Thyroid hormone signaling in the Xenopus laevis embryo is functional and susceptible to endocrine disruption. Endocrinology 153 (10), 5068-5081.

同被引文献8

引证文献6

二级引证文献15

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部