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Distinct roles for MEKK2 and MEKK3 in cell signaling, gene regulation and development as defined by targeted gene disruption.

机译:MEKK2和MEKK3在细胞信号传导,基因调控和发育中的不同作用,如靶向基因破坏所定义。

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摘要

Mitogen activated protein kinase kinase kinases (MAP3Ks) are required for the signal transduction of specific stimuli to activate MAPK cascades, ultimately resulting in a cellular response. MEKKs are a family of kinases at the level of the MAP3Ks comprised of four family members: MEKK1, MEKK2, MEKK3, and MEKK4. MEKK2 and MEKK3 are the most structurally similar of the MEKKs: 65% homologous in the amino-terminal region and 94% homologous within the kinase domain. To delineate the explicit signaling pathways mediated by MEKK2 and MEKK3 in a physiological setting, targeted gene disruption of the two kinases was employed.; The homozygous deletion of MEKK3 resulted in an embryonic lethality between day E3.5 and E6.5. Additionally, MEKK3 is necessary for proliferation of embryonic stem cells and trophoblast stem cells, but not for the initial cellular differentiation of the blastocyst into the embryonic stem cell and trophoblast lineages. Because of the early stage lethality and thus the inability to obtain MEKK3 knockout cells, RNAi was employed to address the role for MEKK3 in MEFs. In MEFs, MEKK3 is necessary for osmotic stress-induced signaling through p38 and ERK5, but not necessary for growth factor regulated induction of MAPK modules, unlike MEKK2.; MEKK2 knockout mice are viable and fertile. Demonstrated in knockout MEKK2 MEFs, MEKK2 expression is required for growth factor activation of the ERK5 and JNK MAPK signaling pathways. Moreover, MEKK2 is required for growth factor induced synthesis of c-Jun and Fra-1 as shown by RPA analysis. Additionally, cytokine expression of IL-1, IL-6 and TNFalpha is mediated by growth factor stimulation through MEKK2. Therefore, MEKK2 coordinately regulates two MAPK pathways in response to growth factors, ERK5 and JNK, resulting in the integrated regulation of AP-1 transcription complexes and ultimately cytokine expression.; As shown by targeted gene disruption and RNAi knockdown, MEKK3 is necessary for embryogenesis, whereas MEKK2-/- mice are viable and fertile. MEKK2 is necessary for growth factor-induced activation of ERK5 and JNK in MEFs, whereas, MEKK3 is necessary for stress-induced activation of ERK5 and p38 in MEFs. Therefore, MEKK2 and MEKK3 have distinct roles in terms of cell signaling, gene regulation and development.
机译:丝裂原活化的蛋白激酶激酶激酶(MAP3Ks)是特定刺激信号转导以激活MAPK级联反应所必需的,最终导致细胞反应。 MEKK是在MAP3K级别上由四个家族成员组成的激酶家族:MEKK1,MEKK2,MEKK3和MEKK4。 MEKK2和MEKK3在结构上与MEKK最为相似:在氨基末端区域具有65%的同源性,在激酶域内部具有94%的同源性。为了描述在生理环境中由MEKK2和MEKK3介导的显性信号通路,采用了两种激酶的靶向基因破坏。 MEKK3的纯合缺失导致在E3.5天至E6.5天之间的胚胎致死率。另外,MEKK3对于胚胎干细胞和滋养层干细胞的增殖是必需的,但对于胚泡向胚胎干细胞和滋养层谱系的初始细胞分化不是必需的。由于早期杀伤力并因此无法获得MEKK3敲除细胞,因此使用RNAi来解决MEKK3在MEF中的作用。在MEF中,与MEKK2不同,MEKK3对于渗透压诱导的通过p38和ERK5的信号传导是必需的,但对于生长因子调节的MAPK模块的诱导则不是必需的。 MEKK2基因敲除小鼠是活的和肥沃的。在敲除MEKK2 MEF中证实,MEKK2表达对于ERK5和JNK MAPK信号通路的生长因子激活是必需的。此外,如RPA分析所示,MEKK2是生长因子诱导的c-Jun和Fra-1合成所必需的。此外,IL-1,IL-6和TNFalpha的细胞因子表达是通过MEKK2刺激生长因子介导的。因此,MEKK2响应生长因子ERK5和JNK协同调节两个MAPK途径,从而导致对AP-1转录复合物的整合调节,并最终调节细胞因子的表达。如靶向基因破坏和RNAi敲除所示,MEKK3是胚胎发生所必需的,而MEKK2-/-小鼠则具有活力和繁殖力。 MEKK2对于MEF中生长因子诱导的ERK5和JNK激活是必需的,而MEKK3对于MEF中应激诱导的ERK5和p38激活是必需的。因此,MEKK2和MEKK3在细胞信号传导,基因调控和发育方面具有独特的作用。

著录项

  • 作者单位

    University of Colorado Health Sciences Center.;

  • 授予单位 University of Colorado Health Sciences Center.;
  • 学科 Biology Molecular.; Health Sciences Pharmacology.; Biology Animal Physiology.
  • 学位 Ph.D.
  • 年度 2002
  • 页码 115 p.
  • 总页数 115
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子遗传学;药理学;生理学;
  • 关键词

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