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转录因子Oct-4调控下游靶基因及其与胚胎发育全能/多能性的关系 被引量:3

Regulation of Downstream Target Genes of Transcription Factor Oct-4 and Its Relationship with Toti/pluripotency of Embryonic Development
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摘要 作为一个和胚胎发育全能/多能性相关的转录因子,Oct-4通过多种多样的调控机制激活或抑制不同靶基因的转录,从而在细胞的全能/多能性及未分化状态的调控维持中发挥重要的作用。已知受Oct-4调控的靶基因中,不仅有一些重要的转录因子如Rex-1,而且有一些参与重要细胞活动的基因如Fgf-4,因此对Oct-4调控下游靶基因的研究将有助于对其在分化发育中所起作用的进一步了解,同时对全能/多能性这一发育学基本问题及其调控网络有一个新的认识。 As a transcription factor related to toti/pluripotency of embryonic development, Oct-4 activates or represses different target genes via diverse modulation mechanism, thereby plays important roles in regulation and maintenance of cell toti/pluripotent and undifferentiated state. Among the known target genes regulated by Oct-4, there are not only some important transcription factors, for example Rex-1, but also some genes participate in important cellular activities such as Fgf-4. So researches on regulation of downstream target genes of Oct-4 will help us to find out it's role in differentiation and development, and provide new insights into the understanding of toti/pluripotency and it's regulatory net in development.
作者 陈艳玫 姚錱
出处 《细胞生物学杂志》 CSCD 北大核心 2004年第5期445-449,共5页 Chinese Journal of Cell Biology
关键词 哺乳动物 靶基因 OCT-4 转录因子 胚胎发育 Oct-4 target gene toti/pluripotency
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参考文献37

  • 1Scholer HR et al. Nature, 1990, 344:435.
  • 2Okamoto K et al. Cell, 1990, 60:461.
  • 3Rosner MH et al. Nature, 1990, 345:686.
  • 4Herr Wet al. Genes Dev, 1988, 2:1513.
  • 5Herr Wet al. Genes Dev, 1995, 9:1679.
  • 6Rosenfeld MG. Genes Dev, 1991, 5:897.
  • 7Scholer HR. Trends Genet, 1991, 7:323.
  • 8Verrijzer CP et al. Biochim Biophys Acta, 1993, 1173:1.
  • 9Palmieri SL et al. Dev Biol, 1994, 166:259.
  • 10Pesce Met al. Mech Dev, 1998, 71:89.

同被引文献42

  • 1杜娟,卢光琇.维持胚胎干细胞不分化状态的分子机制[J].遗传,2005,27(5):828-832. 被引量:5
  • 2Guangjin Pan,James A Thomson.Nanog and transcriptional networks in embryonic stem cell pluripotency[J].Cell Research,2007,17(1):42-49. 被引量:52
  • 3Kishi M, Mizuseki K, Sasai N, Yamazaki H, Shiota K,Nakanishi S, Sasai Y. Requirement of Sox2-mediated signaling for differentiation of early Xenopus neuroectoderm. Development, 2000,127(4):791-800
  • 4Wiebe MS, Wilder PJ, Kelly D, Rizzino A. Isolation, characterization, and differential expression of the murine Sox-2 promoter. Gene, 2000,246(1-2):383-393
  • 5Kamachi Y, Sockanathan S, Liu Q, Breitman M,Lovell-Badge R, Kondoh H. Involvement of SOX proteins in lens-specific activation of crystallin genes. EMBO J, 1995, 14(14):3510-3519
  • 6Kamachi Y, Uchikawa M, Kondoh H. Pairing SOX off with partners in the regulation of embryonic development. Trends Genet, 2000,16(4):182-187
  • 7Sasai Y. Roles of Sox factors in neural determination: conserved signaling in evolution? Int J Dev Biol, 2001,45(1): 321-326
  • 8Murphy FV, Sweet RM, Churchill ME. The structure of a chromosomal high mobility group protein-DNA complex reveals sequence-neutral mechanisms important for nonsequence-specific DNA recognition. EMBO J, 1999,18(23): 6610-6618
  • 9Basilico C, Moscatelli D. The FGF family of growth factors and oncogenes. Adv Cancer Res, 1992,59:115-165
  • 10Lee Niswander, Cheryll Tickle, Astrid Vogel, lain Booth, Gail R. Martin. FGF-4 replace the apical ectodermal ridge and direct outgrowth and patterning of the limb. Cell, 1993,75(3) 579-587

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