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Sirt1基因的研究进展 被引量:5

Research progression of Sirt1
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摘要 Sirtuins家族成员之一,Sirt1(Sirtuin type1)是依赖于烟酰胺腺嘌呤二核苷酸(NAD+),在体内与多种组蛋白和非组蛋白为底物,通过去乙酰化作用来调节其活性的一种组蛋白脱乙酰酶。广泛参与调控哺乳动物细胞寿命的信号及糖代谢、胰岛素分泌等多条代谢通路,对代谢综合征、细胞凋亡、心血管疾病和神经退行性疾病等发挥重要的作用。Sirt1可作为治疗不同疾病的靶点逐渐被人们所重视。 A member of the conserved sirtuin family, Sirtl (Sirtuin typel) is a NAD+ dependent protein deacetylase, which has been shown to deacet)late a wide range of non-histone substrates and histone substrates to regulate their activities. Therefore, Sirtl is characteristically involved in the regulation of several crucial cellular signal pathways in- cluding different signal pathways to regulate mammalian lifespan, glueoneogenesis and insulin secretion and so on. It has been reported that Sirtl extensively participate in the occurrence of metabolic syndrome, cell apoptosis, cardiovascular disease, neurodegenerative diseases and so on. In a word, Sirtl could be emphasized as a new therapy target for many different diseases.
机构地区 深圳大学医学院
出处 《中国医药导报》 CAS 2015年第36期45-48,52,共5页 China Medical Herald
基金 中国博士后科学基金面上资助项目(2015M572369)
关键词 SIRT1 去乙酰化酶 疾病靶点 Sirtl Protein deaceLylase Disease target
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参考文献36

  • 1Kahyo T, Mostoslavsky R, Goto M, et al. Sirtuin-mediated deacetylation pathway stabilizes Wemer syndrome protein [J]. FEBS Lett, 2008,582(17) : 2479-2483.
  • 2Ma Y, Nie H, Chen H,et al. NAD+/NADH metabolism and NAD*-dependent enzymes in cell death and ischemic brain injury:current advances and therapeutic implica- tions [J]. See comment in PubMed Commons below Curt Med Chem, 2015,22(10) : 1239-1247.
  • 3Tanny JC,Moazed D, Coupling of histone decetylation to NAD breakdown by yeast silencing protein Sir2:Evidence of acetyl transfer from substrate to an NAD breakdown product [J]. Proc Natl Acad Sci UAS,2001,98 (2):415- 420.
  • 4Van Leeuwen IM, Higgins M, Campbell J, et al. Modulation of p53 C-terminal acetylation by mdm2,pl4ARF,and cy- toplasmic SirT2 [J]. Mol Cancer Ther,2013,12 (4) :471- 480.
  • 5Motta MC, Divecha N, LemieuxM,et al. Mammalian SIRTI represses forkhead transcription factors [J]. Cell, 2004, 116 (4) :551-563.
  • 6Picard F, Kurtev M, Chung N, et al. Sirtl promotes fat mo- bilization in white adipocytes by repressing PPAR2",/ [J]. Nature, 2004,429 (6993) : 771-776.
  • 7Lu J,Zhang L,Chen X,Lu Q,et al. SIRT1 counteracted the activation of STAT3 and NF-s:B to repress the gastric cancer growth [J]. Int J Clin Exp Med. 2014,17(12): 5050-5058.
  • 8Rodgers JT,Lerin C,Haas W,et al. Nutrient control of glucose homeostasis through a complex of PGC-lalpha and SIRT 1 [J]. Nature, 2005,434 (7029) : 113-118.
  • 9Fulco M,Schihz RL,Iezzi S,et al. Sirt2 regulates skeletal muscle differentiation as a potential sensor of the redox state [J]. Mol Ce11,2003,12(1) :51-62.
  • 10Salminen A, Kaarniranta K. SIRT1 :regulation of longevity via autophagy [J]. Cell Signal, 2009,21 (9) : 1356-1360.

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