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14—3—3蛋白与脂代谢的研究进展

Research progress of 14-3-3 protein and lipid metabolism
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摘要 酪氨酸3-加单氧酶/色氨酸5-加单氧酶激活蛋白(14-3-3蛋白)家族是真核细胞中普遍存在、高度保守的酸性蛋白家族,作为一种新型衔接蛋白可与细胞中多种蛋白相互作用参与细胞的多种调节过程,如细胞凋亡、代谢.近年来很多研究发现14-3-3蛋白与许多与脂代谢相关蛋白质相关联,可作为脂代谢紊乱疾病治疗的新靶点.本文主要简述了14-3-3蛋白家族在脂代谢及脂代谢相关疾病中发挥的作用. Tyrosine-3-monooxy genase/tryptophane-5-monooxy-genase activator protein ( 14-3-3 protein ) is a family of highly conservative and widely expressed acidic polypeptides in all eukaryotic cells. The 14-3-3 protein family consists of adaptors and scaffolds that participates in many cellular processes, such as apoptosis and metabolism. Recent studies have found that 14-3-3 protein is associated with many proteins related to lipid metabolism. It could be exploited for therapy of lipid metabolism disorders. This paper briefly describes the role of the 14-3-3 protein in the lipid metabolism and its related diseases.
出处 《中华内分泌代谢杂志》 CAS CSCD 北大核心 2017年第12期1093-1096,共4页 Chinese Journal of Endocrinology and Metabolism
基金 国家自然科学基金面上项目(81570778)
关键词 14—3—3蛋白 脂代谢 14-3-3 protein Lipid metabolism
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  • 1Mendez HM, Opitz JM. Noonan syndrome: a review [J]. AmJMedGenet, 1985, 21(3): 493-506.
  • 2Tidyman WE, Rauen KA. The RASopathies: develop- mental syndromes of Ras/MAPK pathway dysregulation [J]. Curr Opin Genet Dev, 2009, 19(3): 230-236.
  • 3Tartaglia M, Zampino G, Gelb BD. Noonan syndrome: clinical aspects and molecular pathogenesis [J]. Mol Syndro- mol, 2010, 1(1): 2-26.
  • 4van der Burgt I, Berends E, Lommen E, et al. Clinical and molecular studies in a large Dutch family with Noonan syndrome [J].Am J Med Genet, 1994, 53(2): 187-191.
  • 5Romano AA, Allanson JE, Dahlgren J, et al. Noonan syndrome : clinical features, diagnosis, and management guidelines [J]. Pediatrics, 2010, 126(4): 746-759.
  • 6Yoon SR, Choi SK, Eboreime J, et al. Age-dependent germline mosaicism of the most common Noonan syndrome mutation shows the signature of germline selection [J]. Am J Hum Genet, 2013, 92(6): 917-926.
  • 7Lee YS, Ehninger D, Zhou M, et al. Mechanism and treatment for learning and memory deficits in mouse models of Noonan syndrome [J]. Nat Neurosci, 2014, 17(12): 1736-1743.
  • 8Tartaglia M, Kalidas K, Shaw A, et al. PTPNll muta- tions in Noonan syndrome: molecular spectrum, geno- type-phenotype correlation, and phenotypic heterogeneity [J]. Am J Hum Genet, 2002, 70(6): 1555-1563.
  • 9Lepri F, De Luca A, Stella L, et al. SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations [J]. Hum Mutat, 2011, 32(7): 760-772.
  • 10Gremer L, Merbitz-Zahradnik T, Dvorsky R, et al. Germline KRAS mutations cause aberrant biochemical and physical properties leading to developmental disorders [J]. HumMutat, 2011, 32(1): 33-43.

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