Institute of Biological Chemistry, Academia Sinica, 128, Academia Road Sec 2, Nankang, Taipei 115, Taiwan.
Int J Biol Sci. 2012;8(5):761-77. doi: 10.7150/ijbs.4036. Epub 2012 May 31.
The tristetraprolin (TTP) family comprises zinc finger-containing AU-rich element (ARE)-binding proteins consisting of three major members: TTP, ZFP36L1, and ZFP36L2. The present study generated specific antibodies against each TTP member to evaluate its expression during differentiation of 3T3-L1 preadipocytes. In contrast to the inducible expression of TTP, results indicated constitutive expression of ZFP36L1 and ZFP36L2 in 3T3-L1 preadipocytes and their phosphorylation in response to differentiation signals. Physical RNA pull-down and functional luciferase assays revealed that ZFP36L1 and ZFP36L2 bound to the 3' untranslated region (UTR) of MAPK phosphatase-1 (MKP-1) mRNA and downregulated Mkp-1 3'UTR-mediated luciferase activity. Mkp-1 is an immediate early gene for which the mRNA is transiently expressed in response to differentiation signals. The half-life of Mkp-1 mRNA was longer at 30 min of induction than at 1 h and 2 h of induction. Knockdown of TTP or ZFP36L2 increased the Mkp-1 mRNA half-life at 1 h of induction. Knockdown of ZFP36L1, but not ZFP36L2, increased Mkp-1 mRNA basal levels via mRNA stabilization and downregulated ERK activation. Differentiation induced phosphorylation of ZFP36L1 through ERK and AKT signals. Phosphorylated ZFP36L1 then interacted with 14-3-3, which might decrease its mRNA destabilizing activity. Inhibition of adipogenesis also occurred in ZFP36L1 and TTP knockdown cells. The findings indicate that the differential expression of TTP family members regulates immediate early gene expression and modulates adipogenesis.
Tristetraprolin (TTP) 家族包含锌指结构域含有 AU 丰富元件 (ARE) 的结合蛋白,由三个主要成员组成:TTP、ZFP36L1 和 ZFP36L2。本研究针对每个 TTP 成员生成了特异性抗体,以评估其在 3T3-L1 前脂肪细胞分化过程中的表达。与 TTP 的诱导表达相反,结果表明 ZFP36L1 和 ZFP36L2 在 3T3-L1 前脂肪细胞中组成性表达,并对分化信号发生磷酸化。物理 RNA 下拉和功能荧光素酶测定显示,ZFP36L1 和 ZFP36L2 结合到 MAPK 磷酸酶-1 (MKP-1) mRNA 的 3'非翻译区 (UTR),并下调 Mkp-1 3'UTR 介导的荧光素酶活性。Mkp-1 是一种即刻早期基因,其 mRNA 对分化信号的短暂表达。Mkp-1 mRNA 的半衰期在诱导 30 分钟时比在诱导 1 小时和 2 小时时更长。TTP 或 ZFP36L2 的敲低增加了诱导 1 小时时 Mkp-1 mRNA 的半衰期。敲低 ZFP36L1,但不是 ZFP36L2,通过 mRNA 稳定化增加了 Mkp-1 mRNA 的基础水平,并下调了 ERK 激活。分化通过 ERK 和 AKT 信号诱导 ZFP36L1 磷酸化。磷酸化的 ZFP36L1 然后与 14-3-3 相互作用,这可能会降低其 mRNA 不稳定活性。脂肪生成的抑制也发生在 ZFP36L1 和 TTP 敲低细胞中。这些发现表明 TTP 家族成员的差异表达调节即刻早期基因表达并调节脂肪生成。