CHEN Rui,LI Jian-xiang,NIE Ji-hua,SHI Min-hua,HU Hua-cheng,TONG Jian.Construction and identification of differential expression genes of peripheral blood cells in radon-exposed mice[J].Chinese Journal of Radiological Medicine and Protection,2009,29(1):17-19
Construction and identification of differential expression genes of peripheral blood cells in radon-exposed mice
Received:August 28, 2008  
DOI:10.3760/cma.j.issn.0254-5098.2009.01.005
KeyWords:Radon  Suppression subtractive hybridization  Differential expression genes  Bioinformatics
FundProject:国家自然科学基金资助项目(30371226,30671784);教育部博士学科点专项科研基金资助项目(20050285009)
Author NameAffiliationE-mail
CHEN Rui Department of Respiratory Diseases, Second Affiliated Hospital of Soochow University, Suzhou 215004, China  
LI Jian-xiang 苏州大学放射医学与公共卫生学院卫生毒理学教研室  
NIE Ji-hua 苏州大学放射医学与公共卫生学院卫生毒理学教研室  
SHI Min-hua Department of Respiratory Diseases, Second Affiliated Hospital of Soochow University, Suzhou 215004, China  
HU Hua-cheng Department of Respiratory Diseases, Second Affiliated Hospital of Soochow University, Suzhou 215004, China  
TONG Jian 苏州大学放射医学与公共卫生学院卫生毒理学教研室 tongjian@suda.edu.cn 
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Abstract::
      Objective To screen and identify the differential expression genes on peripheral blood cells of mice based on the experimental animal model of radon exposure.Methods BALB/c mice were exposed in a type HD-3 multifunctional radon-room, with the accumulative doses of radon-exposure group at 105 WLM and control group at 1 WLM. Total RNA was extracted from peripheral blood cells and the methods of SMART for dscDNA synthesis and SSH for gene screening was applied. With the construction of the cDNA library enriched with differentially expressed genes,the pMD 18-T plasmid containing LacZ operator at the multiple cloning site was used to allow a blue_white screening. The TA clones were amplified by nested PCR and the reverse Northern blot was used to identify up and down regulation of the clones. The differently expressed cDNA was then sequenced and analyzed.Results The subtracted cDNA libraries were successfully constructed. A total of 390 recombinant white colonies were randomly selected. Among the 312 cDNA monoclones selected from both forward- and reverse-subtracted libraries,41 clones were chosen to sequence for their differential expressions based on reverse Northern blot. Among the 41 sequenced clones,10 clones with known function/annotation and 3 new ESTs with the GenBank accession numbers were obtained. Most of the known function/annotation genes were revealed to be related with cell proliferation,metabolism,cellular apoptosis and carcinogenesis.Conclusion The animal model of radon exposure was established and the cDNA library of peripheral blood cells was successfully constructed. Radon exposure could up- and down-regulate a series of genes. Differentially expressed genes could be identified by using SSH technique and the results may help exploring mechanisms of random exposure.
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