期刊文献+

细胞周期相关蛋白DCT1染色体及细胞定位与其组织表达的研究

Chromosomal and Subcellular Localization and Expression of Cell Cycle-related Regulator DCT1
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摘要 目的对候选抑癌基因DOC-1R((Deleted in oral cancer-1 related,CDK2AP2)相关基因DCT1(DOC-1Rterminal1)进行染色体定位分析并观察其细胞内定位,检测该基因在人类组织中的表达。方法通过辐射杂交细胞系对其进行染色体定位分析,同时构建EGFP-DCT1质粒并转染HeLa细胞,荧光显微镜观察DCT1蛋白在细胞内的定位。此外,应用荧光定量PCR的方法检测该基因在16个正常人类组织中的表达。结果DCT1基因定位于5q31,其编码产物在HeLa细胞中定位于核膜,该基因在正常人类的16个组织中均有表达,其中在脾中表达水平较高。结论DCT1可能为细胞周期调控相关基因,在人类组织中普遍表达。 Objective To investigate the chromosomal and subcellular localization of DOC-1R teiminal 1 ( DCT1 ),and detect its expression in human tissues. Methods Chromosome localization of DCTI was detected by radiation hybrid, pEGFP-DCT1 was constructed, and HeLa cells were transfected with the plasmid. The subcellular localization of DCT1 protein was observed by fluorescence microscope. Real-time PCR was performed for the determination of DCTI expression level in 16 kinds of human tissues. Results DCTI was demonstrated to localize in 5q31,and its encoding protein was detected on the nuclear membrane. Additionally,DCTl was proved to express universally in all the 16 kinds of human tissues and it was expressed at the highest level in spleen. Conclusion DCT1 might be a regulator in cell cycle,and ubiquitously express in human tissues.
出处 《中国医科大学学报》 CAS CSCD 北大核心 2010年第2期105-107,111,共4页 Journal of China Medical University
基金 辽宁省教育厅重点实验室项目(20060908) 辽宁省教育厅创新团队项目(2008T194)
关键词 DCT1基因 DOC-1R基因 染色体定位 细胞定位 基因表达 DCTI gene DOC-1R gene chromosomal localization subcellular localization gene expression
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参考文献10

  • 1Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2^-△△CT method [J]. Methods, 2001,25(4) :402-408.
  • 2Zhang X,Tsao H, Tsuji T, et al. Identification and mutation analysis of DOC-1R,a DOC-1 growth suppressor-related gene [J]. Biochem Biophys Res Commun, 1999,225 ( 1 ) : 59-63.
  • 3Terret EM,Lefebvre C,Djiane A,et al. DOC1R:a MAP kinase substrate that control microtubule organization of metaphase II mouse oocytes[ J ]. Development, 2003,130(21 ) :5169-5177.
  • 4生秀杰,姜莉,周伟强,王太一,张学.应用基因组步移克隆小鼠Doc-1R基因组序列[J].中华医学遗传学杂志,2001,18(4):314-316. 被引量:12
  • 5生秀杰,周伟强,姜莉,张梅英,王太一,张学.小鼠Doc-1R基因的克隆及其表达[J].癌症,2002,21(2):122-122. 被引量:4
  • 6周伟强,姜莉,生秀杰,张学.小鼠DOC-1R反义重组载体的构建及表达的研究[J].癌症,2002,21(3):240-244. 被引量:6
  • 7Dominique AB,Shahul M, Marie-Therese A,et al. Cdk2 associates with MAP kinase in vivo and its nuclear translocation is dependent on MAP kinase activation in IL-2-dependent Kit 225 T lymphocytes [J]. Oncogene, 2000; 19(36) :4184-4189.
  • 8Matsuo K,Shintani S,Tsui T,et al. p12DOC-1 ,a growth suppressor, associates with DNA polymerase α/primase [J]. FASEB J,2000,14 (10) : 1318-1324.
  • 9Shintani S,Ohyama H,Zhang X,et al. p12DOC-1 is a novel cyclin- dependent kinase 2- associated protein [J]. Mol Cell Biol,2000,20 ( 17 ) : 6300-6307.
  • 10Marcotte EM, Pellegrini M, Ng HL, et al. Detecting protein function and protein-protein interaction from genome sequences [J]. Science, 1999,285 (5428) : 751-753.

二级参考文献9

  • 1Bartkova J, Lukas J , Strauss M , et al. Cyclin D1 oncoprotein aberrantly accumulates in malignancies of diverse histogenesis[J]. Oncogene,1995,10:775-778.
  • 2Zhang X, Tsao H, Tsuji T,et al. Identification and mutation analysis of DOC-1R, a DOC-1 growth suppressor-related gene [J]. Biochem Biophys Res Commun, 1999,255(1):59-63.
  • 3J.萨姆布鲁克,EF费里奇,T曼尼阿蒂斯.分子克隆实验指南[M].第1版.北京:科学出版社,1992:110-150.
  • 4Fang X ,Jin X ,Xu HJ , et al .Expression of p16 induces transcriptional downregulation of the RB gene [J]. Oncogene,1998,16(1):1-8.
  • 5Li JM ,Hu PP ,Shen X, et al.E2F 4-RB and E2F 4-p107 complexes suppress gene expression by transforming growth factor beta through E2F binding sites [J]. Proc Natl Acad Sci USA,1997,94(10):4948-4953.
  • 6Hinchcliffe EH, Li C, Thompson EA, et al. Requirement of CDK2-cyclin E activity for repeated centrosome reproduction in Xenopus egg extract [J]. Science, 1999, 283(5403): 851-854.
  • 7Todd R, McBride J, Tsuji T, et al. Deleted in oral cancer-1 (doc-1), a candidate oral tumor suppressor gene [J]. FASEB J, 1995, 9(13):1362-1370.
  • 8桑建利,王永潮,叶颖江.增强p21^(waf1)表达对乳腺癌细胞增殖及G1期cyclin和CDK表达的影响[J].科学通报,1999,44(10):1074-1078. 被引量:4
  • 9胡维,向华,周艳,刘敬忠.用PCR法直接快速筛查重组阳性克隆[J].生物技术通报,1999,15(6):39-40. 被引量:14

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