期刊文献+

Forkhead转录因子调控干细胞的命运决定 被引量:6

Forkhead Transcription Factors Control Stem Cell Fate Determination
原文传递
导出
摘要 Forkhead蛋白是一类在进化上高度保守的重要转录因子家族。目前,已经发现超过100种编码Forkhead蛋白的基因,Forkhead蛋白的典型结构特征是含有Forkhead结构域,即一段由100个氨基酸组成的进化上保守的"Forkhead"DNA结合序列。Forkhead蛋白的主要功能包括调控与胚胎发育、细胞生长、增殖、分化、干细胞干性保持、应激反应、语言形成以及长寿相关基因的表达。Forkhead基因的突变或者调控异常会导致发育缺陷以及肿瘤形成。因此,对于不同Forkhead蛋白家族成员功能的深入研究,有助于更好地揭示相关疾病的发病机制,为针对这些疾病的预防和治疗提供理论依据。该文对国内外Forkhead蛋白在干细胞中的主要功能方面的研究成果进行了总结,综述了近年来的最新研究成果。 Forkhead family, a group of conserved transcription factors existing from yeast to human, is marked by the presence of a 100aa Forkhead DNA binding domain. There have been over 100 genes encoding Forkhead transcription factors being found to date. Forkhead transcription play important roles in regulating many important cell processes including development, cell proliferation, differentiation, sternness maintenance, stress re- sponse, language acquirement, and longevity. Disruption of normal functions of forkhead factors resulted in devel- opmental defects and tumorigenesis. Elucidation of the mechanism governing functions of Forkhead transcription factors will help developing therapies for many human diseases. This review is mainly focused on the functions of forkhead transcription factors, especially Foxo subfamily, in stem ceils.
出处 《中国细胞生物学学报》 CAS CSCD 北大核心 2012年第12期1197-1206,共10页 Chinese Journal of Cell Biology
基金 国家自然科学基金(No.31171420) 中国科学院"百人计划"(No.2012OHTP02) 中国科学院干细胞战略性先导科技专项(No.XDA01010204) 上海市"浦江人才"(No.12PJ1409700)资助项目~~
关键词 Forkhead蛋白 干细胞 转录调控 FoxO蛋白 信号通路 Forkhead transcription factor stem cell transcription regulation Foxo signaling pathways
  • 相关文献

参考文献96

  • 1Tuteja G, Kaestner KH. SnapShot: Forkhead transcription factorsI. Cell 2007; 130(6): 1160.
  • 2Tuteja G, Kaestner KH. Forkhead transcription factors II. Cell2007; 131(1): 192.
  • 3Xie L, Ushmorov A, Leithauser F, Guan H, Steidl C, FarbingerJ, et al. FOXOl is a tumor suppressor in classical Hodgkin lym-phoma. Blood 2012; 119(15): 3503-11.
  • 4Wijchers PJ, J Burbach JP, Smidt MP. In control of biology: ofmice, men and Foxes. Biochem J 2006; 397(2): 233-46.
  • 5Carlsson P, Mahlapuu M. Forkhead transcription factors: Keyplayers in development and metabolism. Dev Biol 2002; 250(1):1-23.
  • 6Clark KL, Halay ED, Lai E, Burley SK. Co-crystal structure ofthe HNF-3/fork head DNA-recognition motif resembles histoneH5. Nature 1993; 364(6436): 412-20.
  • 7Sandri M, Sandri C, Gilbert A, Skurk C, Calabria E, Picard A, etal. FoxO transcription factors induce the atrophy-related ubiquit-in ligase atrogin-1 and cause skeletal muscle atrophy. Cell 2004;117(3): 399-412.
  • 8Andjelkovic M, Alessi DR, Meier R, Fernandez. A; Lamb NJ,Freeh M, et al. Role of translocation in the activation and func-tion of protein kinase B., J Biol Chem 1.997; 272(50): 31515-24.
  • 9Cirillo LA, Lin FR, Cuesta I, Friedman D, Jamik M, Zaret KS.Opening of compacted chromatin by early developmental tran-scription factors HNF3 (FoxA) and GATA-4. Mol Cell 2002;9(2): 279-89.
  • 10Friedman JR, Kaestner KH. The Foxa family of transcriptionfactors in development and metabolism. Cell Mol Life Sci 2006;63(19/20):2317-28.

同被引文献97

  • 1王静.猪肉品质的品种差异与营养调控及其机制研究[D].雅安:四川农业大学,2012.
  • 2杨燕军,白亮,庞卫军,杨公社.猪FoxO1基因cDNA部分序列的克隆及其组织表达[J].畜牧兽医学报,2007,38(11):1143-1148. 被引量:3
  • 3Weigel D, Jtirgens G, Ktittner F, et al.The homeotic gene fork head encodes a nuclear protein and is expressed in the terminal regions of the Drosophila embryo [J] . Cell, 1989, 57 ( 4 ) : 645 -658.
  • 4Kousteni S.FoxO1, the transcriptional chief of staff of energy metabolism [J]. Bone, 2012,50 ( 2 ) : 437- 443.
  • 5Hu P, Geles K G, Paik J H, et al. Codependent activators direct myoblast- specific MyoD transcription [J]. Developmental cell, 2008,15 ( 4 ) : 534-546.
  • 6Kamei Y, Miura S, Suzuki M, et al. Skeletal muscle FoxO1 (FKHR)transgenic mice have less skeletal muscle mass,down- regulated Type I ( slow twitch/red muscle ) fiber genes, and impaired glycemic control [J] . Journal of Biological Chemistry, 2004,279 (39) :41114-41123.
  • 7Romanello V, Guadagnin E, Gomes L, et al. Mitochondrial fission and remodelling contributes to muscle atrophy [J]. The EMBO journal, 2010,29 ( 10 ) : 1774-1785.
  • 8Chen C C, Jeon S M, Bhaskar P T, et al. FoxOs inhibit mTORC1 and activate Akt by inducing the expression of Sestrin3 and Rictor[J].Developmental cell,2010,18 (4) :592-604.
  • 9Reed S A, Senf S M, Cornwell E W, et al. Inhibition of IkappaB kinase alpha ( IKKα ) or IKKbeta ( IKKβ ) plus forkhead box O ( FoxO ) abolishes skeletal muscle atrophy [J]. Biochemical and biophysical research communications, 2011, 405 ( 3 ) : 491-496.
  • 10Clavel S, Siffroi- Fernandez S, Coldefy A S, et al. Regulation of the intracellular localization of FoxO3a by stress- activated protein kinase signaling pathways in skeletal muscle cells [J]. Molecular and cellular biology ,2010,30 (2) :470-480.

引证文献6

二级引证文献13

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