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小鼠胚胎干细胞核心转录因子nanog靶基因Zbtb9的生物信息学分析

Bioinformaton Analysis of Zbtb9 Gene of Mouse Embryonic Stem Cells Transcription Factor Nanog Downstream
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摘要 通过特异性引物用RT-PCR方法扩增Zbtb9基因。利用生物信息学对小鼠的Zbtb9基因启动子进行生物信息学分析,预测Zbtb9基因启动子位置和启动子区内含有的转录因子结合位点,以及nanog在Zbtb9基因转录调控中的作用及Zbtb9蛋白的基本性质。Zbtb9基因启动子区可能定位于转录起始点上游790 bp至1024 bp之间。启动子区内含有15个转录调控因子结合位点,nanog的作用靶序列位于Zbtb9基因启动子区与转录起始位点之间,提示nanog在Zbtb9基因转录调控中起作用,小鼠Zbtb9蛋白二级结构可能以螺旋为主,富含疏水性氨基酸;对Zbtb9基因疏水区的氨基酸进行跨膜区分析,提示可能是跨膜蛋白。经SMART分析,Zbtb9蛋白含有BTB/POZ结构域。 Zbtb9 gene was amplified by reverse transcription-polymerase chain reaction(RT-PCR) using the special primers.To analyze the Zbtb9 genes using bioinformatics tools and predict the promoter position and transcription factor binding sites Methods.Predict the function of nanog in the Zbtb9 genes transcription regulation.Predict the Zbtb9 protein by bioinformatic methods.The promoter of zbtb9 was located in 790-1024bp of up-steam of transcriptional site.Transcription factor binding sites of zbtb9 was found with 15 transcription factors.The nanog taget sequence located between promoter region and transcriptional site showed that nanog play an important role in Zbtb9 genes transcription regulation.The transmembrane analysis of the amino acids demonstrated that the secondary structure was helix and this protein contain a transmembrane domain mainly could be transmembrane protein.Zbtb9 cotain BTB/POZ domain by SMART analying.
作者 曹峰 李裕强
出处 《西北农业学报》 CAS CSCD 北大核心 2008年第5期21-25,共5页 Acta Agriculturae Boreali-occidentalis Sinica
关键词 小鼠干细胞转录因子 NANOG基因 Zbtb9基因 生物信息学分析 Mouse embryonic stem cells transcription factor,Nanog gene,Zbtb9gene,Bioinformatics analysis
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参考文献14

  • 1ChamBers I, Colby D, Robertson M, et al. Functional expression cloning of Nanog, a pluripotency sustaining factor in embryonic stem cells[J]. Cell, 2003, 113:643-655.
  • 2Mitsui K, ToKuzawa Y,Itoh H, et al. The homeoprotein Nanog is required for maintenance of pluripotency in mouse epiblast and ES cells[J]. Cell, 2003, 113:631-642.
  • 3Yamaguchi S, Kimura H, Tada M, et al. Nanog expression in mouse germ cell development[J]. Gene Expr Patterns, 2005, 5:639-646.
  • 4Strumpf D, Mao C A, Yamanaka Y, et al . Cdx2 is required for correct cell fate specification and differentiation of trophectoderm in the mouse blastocys[J]. Development, 2005, 132:2093-102.
  • 5Loh Y H, Wu Q, Chew J L, et al. The Oct4 and Nanog transcription network regulates pluripotency in mouse embryonic stem cells[J]. Nat. Genet, 2006, 38:431-440.
  • 6Giacomelli L, Nieolini C. Gene expression of human T lym phoeytes cell cycle: experimental and bioinformatic analysis [J]. Cell Bio2chem, 2006, 22:1-12.
  • 7宋凯,宋继梅,张涌.小鼠Oct4基因的克隆及其原核表达载体的构建[J].西北农业学报,2006,15(5):10-13. 被引量:2
  • 8李巍主编.生物信息学导论[M].河南:郑州大学出版社,2001.
  • 9[美]乔纳森·佩夫斯纳著.孙之荣译.生物信息学与功能基因组学[M].北京:化学工业出版社,2006.
  • 10Turner B C, ZHANG J, Gumbs A A, et al. Expression of AP-2 transcription factors in human breast cancer corre lates with the regulation of multiple growth factor signaling pathways[J]. Cancer Res, 1998, 58(23) :5466-5472.

二级参考文献18

  • 1丛笑倩,李秀兰,徐洁,沈鼎武,姚錱.人抗药基因在小鼠ES细胞中的表达及嵌合体小鼠的研究[J].实验生物学报,1993,26(4):429-439. 被引量:1
  • 2陆德裕.哺乳动物嵌合体[J].细胞生物学杂志,1982,4(1):7-14.
  • 3赖良学 孙青原 等.哺乳动物胚胎干细胞的研究进展[J].生物技术学报,1993,(3):1-4.
  • 4赖良学,生物技术学报,1993年,3期,1页
  • 5徐浩,实验生物学报,1991年,24卷,2期,353页
  • 6汪德耀,普通细胞生物学,1988年,364页
  • 7陆德裕,细胞生物学杂志,1982年,4卷,1期,7页
  • 8Brehm A, Ovitt C E, Scholer H R. Oct-4: more than just a POU erful marker of the mammalian germline[J]. APMIS,1998, 106, 114-124.
  • 9DU Juan , I.IN Ge, I.U Guang Xiu. Screening of Differential Genes Between Human Embryonic Stem Cell and Differentiated Cell[J]. Acta Genetica Sinica, 2004 , 31 (9)956 -962.
  • 10KarinH, Fu hrmannG, ChristenssonK, et al. Derivation of oocytes from mouse embryonic stem cells[J]. Sience, 2003, 300(23) :1251-1256.

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