Laboratory of Epileptogenesis, Nencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur Street, 02-093, Warsaw, Poland.
Neurochem Res. 2021 Sep;46(9):2463-2472. doi: 10.1007/s11064-021-03374-2. Epub 2021 Jun 26.
Tweety-homolog 1 protein (Ttyh1) is abundantly expressed in neurons in the healthy brain, and its expression is induced under pathological conditions. In hippocampal neurons in vitro, Ttyh1 was implicated in the regulation of primary neuron morphology. However, the mechanisms that underlie transcriptional regulation of the Ttyh1 gene in neurons remain elusive. The present study sought to identify the promoter of the Ttyh1 gene and functionally characterize cis-regulatory elements that are potentially involved in the transcriptional regulation of Ttyh1 expression in rat dissociated hippocampal neurons in vitro. We cloned a 592 bp rat Ttyh1 promoter sequence and designed deletion constructs of the transcription factors specificity protein 1 (Sp1), E2F transcription factor 3 (E2f3), and achaete-scute homolog 1 (Ascl1) that were fused upstream of a luciferase reporter gene in pGL4.10[luc2]. The luciferase reporter gene assay showed the possible involvement of Ascl1, Sp1, and responsive cis-regulatory elements in Ttyh1 expression. These findings provide novel information about Ttyh1 gene regulation in neurons.
Tweety-homolog 1 蛋白(Ttyh1)在健康大脑中的神经元中大量表达,其表达在病理条件下被诱导。在体外海马神经元中,Ttyh1 被牵连到调节原代神经元形态。然而,神经元中 Ttyh1 基因转录调控的机制仍不清楚。本研究旨在鉴定 Ttyh1 基因的启动子,并对潜在参与体外大鼠分离海马神经元中 Ttyh1 表达转录调控的顺式调控元件进行功能表征。我们克隆了一个 592bp 的大鼠 Ttyh1 启动子序列,并设计了特异性蛋白 1(Sp1)、E2F 转录因子 3(E2f3)和 achaete-scute 同源物 1(Ascl1)的缺失构建体,这些构建体融合在 pGL4.10[luc2]中的荧光素酶报告基因的上游。荧光素酶报告基因检测表明 Ascl1、Sp1 和反应性顺式调控元件可能参与 Ttyh1 的表达。这些发现为神经元中 Ttyh1 基因调控提供了新的信息。