期刊文献+

生物异源物质对小球藻基因转录研究体系的建立(英文)

ESTABLISHMENT OF REAL-TIME PCR FOR ANALYZING mRNA ABUNDANCE IN CHLORELLA VULGARIS EXPOSED TO XENOBIOTICS
下载PDF
导出
摘要 藻类是水生生态系统中的敏感物种。在环境生物学研究中,基因转录水平通常作为衡量基因表达水平变化的指标。研究建立了定量PCR技术(Real-time PCR)检测小球藻基因转录变化的研究体系。以3个主要光合作用基因(psaB、psbC、rbcL)为靶标基因,研究了除草剂草丁瞵(Glufosinate)、阿特拉津(Atrazine)和禾草灵(Diclofop-methyl)对基因转录的影响,结果表明3种供试药物对小球藻光合作用基因psbC和rbcL相对表达量有显著地抑制作用。这表明Real-time PCR可以作为评定水生环境中异源化合物毒性的有效方法。 Among the aquatic organisms, algae are one of the most susceptible organisms to pollution in water. Transcriptional abundance has been gradually used as a surrogate for gene expression in environmental biology. In the present study, real-time PCR assay was established to quantify the transcript abundances of three pbotosystem genes (psaB, psbC and rbcL) in Chlorella vulgaris, and the acute toxicity of three herbicides (glufosinate, atrazine and diclofop-methyl) was assessed using this method. The results demonstrated that real-time PCR is an efficient technique to assess the toxicity of xenobiotic compounds in aquatic system.
出处 《水生生物学报》 CAS CSCD 北大核心 2010年第1期139-143,共5页 Acta Hydrobiologica Sinica
基金 National nature Science Foundation of "Enantioselectivity of toxicities and molecular mechanisms in chiral herbicides" Natural Science Foundation of China(20607020) Ministry of Education Key Lab of Environment Remediation and Ecological Health of China(EREH0709)
关键词 REAL-TIME PCR 普通小球藻 光合作用 基因转录 Real-time PCR Chlorella vulgaris Photosynthesis Transcript abundance
  • 相关文献

参考文献2

二级参考文献22

  • 1陈加平,傅文宇,王秀敏,徐立红.微囊藻毒素LR对BRL-3A凋亡相关蛋白表达的影响[J].中国环境科学,2004,24(4):460-463. 被引量:6
  • 2王秀敏,陈加平,傅文宇,徐立红.活体染毒时藻毒素LR诱导大鼠肝脏P53和Bax蛋白的表达[J].浙江大学学报(医学版),2005,34(3):220-222. 被引量:3
  • 3乔雄梧,马利平.阿特拉津在土壤中的降解途径及其对持留性的影响[J].农村生态环境,1995,11(4):5-8. 被引量:25
  • 4Carmichael W W. The toxins of cyanobacteria [J]. Sci Am, 1994, 270: 64 - 72.
  • 5Hallegreff G M. A review of harmful algal blooms and their apparent global increase [J]. Phycologia, 1993,32:79-99.
  • 6Pouria S, D E Andrade A, Barbosa J, et al. Fatal microcystin intoxication in haemodialysis unit in Caruaru, Brazil [J]. Lancet, 1998, 352 : 21-26.
  • 7Mcdermott C M, Nho C W, Howard W, et al. The cyanobactefia toxin, microcystin-LR can induce apoptosis in a variety of cell types [J]. Toxicon, 1998,36 : 1981-1996.
  • 8Gudas J M, Payton M, Thukral S, et al. Cyclin E2,a novel G1 cyclin that binds CDK2 and is aberrantly expressed in human cancers [J]. Mol . Cell. Biol , 1999,19:612-622.
  • 9Zariwala M, Liu J, Xiong Y M.Cyclin E2,a novel human G1 cyclin and activating partner of CDK2 and CDK3, is induced by viral oncoproteins [ J]. Oncogene, 1998,17 : 2787-2798.
  • 10Lauper N, Beck A R, Cariou S, et al. Cyclin E2: a novel CDK2 partner in the late G1 and S phases of the mammalian cell cycle [J]. Oncogene , 1998,17:637-2643.

共引文献120

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