Regulation of Placental and Embryonic Development by Tgifs

Tgifs 对胎盘和胚胎发育的调节

• 批准号: 7201753
• 负责人: David Wotton
• 金额: $ 30.04万
• 依托单位: UNIVERSITY OF VIRGINIA
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-02-15 至 2012-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7201753
• 关键词: Activins; Affect; Area; Cell Differentiation process; Cessation of life; Defect; Development; Disruption; Embryo; Embryonic Development; Epiblast; Equilibrium; Event; Failure; Fetal Growth Retardation; Fetal Tissues; Gases; Gene Expression; Gene Targeting; Genes; Genetic Transcription; Giant Cells; Guanine; Human; In Situ Hybridization; In Vitro; Labyrinth; Mammalian Cell; Mesoderm; Mothers; Mus; Mutation; Nodal; Nutrient; Pathway interactions; Pattern; Perinatal; Phenotype; Placenta; Placental Insufficiency; Placentation; Pregnancy; Proteins; RXR; Recruitment Activity; Regulation; Reporter; Repression; Retinoic Acid Receptor; Signal Transduction; Site; Smad Proteins; Smad protein; Staging; Stem cells; Surface; Testing; Thymine; Transcription Repressor/Corepressor; Transcriptional Activation; Transforming Growth Factor beta; Transforming Growth Factors; Tretinoin; cell type; derepression; in utero; loss of function; mutant; null mutation; response; stem; trophoblast

DESCRIPTION (provided by applicant): The mammalian placenta provides a large surface area over which exchange of nutrients and gases between the mother and embryo occurs. Placental insufficiency results in intrauterine growth retardation (IUGR), which is the second leading cause of perinatal death, affecting up to 6% of human pregnancies. There is significant conservation of function between mouse and human placenta, and many of the key regulators are also conserved between the two species. Trophoblast stem (TS) cells give rise to all major cell types of the mouse placenta, and correct TS cell differentiation is required for normal placental development. Retinoic acid (RA) and Nodal signaling have opposing effects on TS cell differentiation: RA signaling promotes the formation of trophoblast giant cells at the expense of spongiotrophoblasts, whereas, Nodal decreases giant cell formation. Disruption of either pathway results in aberrant placental development. Tgif (Thymine Guanine Interacting Factor) is a transcriptional corepressor, which limits both TGF beta/Nodal and RA signaling. Tgif recruits general corepressors to activated Smads, limiting the extent of transcriptional activation by TGF beta/Nodal. Tgif interacts with the RXR retinoic acid receptor and represses RA dependent gene expression. A Tgif null mutation in mice causes placental defects, whereas embryos lacking both Tgif and the functionally related Tgif2 die soon after gastrulation. We will test the hypothesis that Tgifs have critical functions in Nodal and RA signaling at different developmental stages: Complete loss of Tgif and Tgif2 function causes gastrulation defects, primarily by derepressing Nodal regulated gene expression. Later in development, RA signaling is sensitive to reduced Tgif function, and derepression of RA-responsive transcription causes defects in TS cell differentiation and placental development. We will test whether the Tgif mutation alters RA and Nodal signaling, causing defects in placental development. We will test whether Tgif regulates TS cell differentiation in vitro by repressing the transcriptional response of TS cells to RA and Nodal. Finally, we will test whether complete loss of Tgif and Tgif2 function causes defects in gastrulation, by derepressing Nodal-activated gene expression resulting in decreased proliferation and defective axis formation. This will determine how Tgifs regulate placental and embryonic development and generate a better understanding of placental insufficiency, embryonic development and intrauterine growth retardation.

描述（由申请人提供）：哺乳动物胎盘提供了一个大的表面积，在这个表面积上，母亲和胚胎之间的营养物质和气体交换发生。胎盘功能不全导致宫内生长迟缓（IUGR），这是围产期死亡的第二大原因，影响到高达6%的人类妊娠。在小鼠和人类胎盘之间存在显著的功能守恒，并且许多关键的调节因子在两个物种之间也存在守恒。滋养细胞干细胞（Trophoblast stem， TS）可以产生小鼠胎盘的所有主要细胞类型，正确的TS细胞分化是胎盘正常发育所必需的。视黄酸（Retinoic acid， RA）和Nodal信号通路对TS细胞分化的影响相反：RA信号通路促进滋养层巨细胞的形成，损害海绵滋养层细胞的形成，而Nodal则抑制巨细胞的形成。任何途径的破坏都会导致胎盘发育异常。Tgif（胸腺嘧啶鸟嘌呤相互作用因子）是一种转录辅抑制因子，限制TGF β /Nodal和RA信号。TGF招募一般的辅抑制因子激活Smads，限制了TGF β /Nodal的转录激活程度。Tgif与RXR维甲酸受体相互作用，抑制RA依赖基因的表达。小鼠中Tgif缺失突变会导致胎盘缺陷，而缺乏Tgif和功能相关的Tgif2的胚胎在原肠胚形成后很快死亡。我们将验证Tgif在不同发育阶段的Nodal和RA信号传导中具有关键功能的假设：Tgif和Tgif2功能的完全丧失主要通过抑制Nodal调节基因表达导致原肠胚发育缺陷。在发育后期，RA信号对Tgif功能的降低很敏感，RA应答转录的抑制会导致TS细胞分化和胎盘发育的缺陷。我们将测试Tgif突变是否会改变RA和Nodal信号，从而导致胎盘发育缺陷。我们将测试Tgif是否通过抑制TS细胞对RA和Nodal的转录反应来调节TS细胞的体外分化。最后，我们将测试Tgif和Tgif2功能的完全丧失是否会导致原肠胚形成缺陷，通过抑制nodal激活基因表达导致增殖减少和轴形成缺陷。这将确定tgfs如何调节胎盘和胚胎发育，并更好地了解胎盘功能不全、胚胎发育和宫内生长迟缓。