Nakamura Mako, Choe Seong-Kyu, Runko Alexander P, Gardner Paul D, Sagerström Charles G
Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, USA.
BMC Dev Biol. 2008 Nov 12;8:108. doi: 10.1186/1471-213X-8-108.
Members of the NET subfamily of zinc-finger proteins are related to the Sp-family of transcription factors and are required during embryogenesis. In particular, Nlz1/Znf703 and Nlz2/Znf503 are required for formation of rhombomere 4 of the vertebrate hindbrain. While NET family proteins have been hypothesized to regulate transcription, it remains unclear if they function as activators or repressors of transcription.
Here we demonstrate that Nlz proteins repress transcription both in cell lines and in developing zebrafish embryos. We first use standard cell culture-based reporter assays to demonstrate that Nlz1/Znf703 represses transcription of a luciferase reporter in four different cell lines. Structure-function analyses and pharmacological inhibition further reveal that Nlz1-mediated repression requires histone deacetylase activity. We next generate a stable transgenic zebrafish reporter line to demonstrate that Nlz1 promotes histone deacetylation at the transgenic promoter and repression of transgene expression during embryogenesis. Lastly, taking a genetic approach we find that endogenous Nlz proteins are required for formation of hindbrain rhombomere 4 during zebrafish embryogenesis by repressing expression of non-rhombomere 4 genes.
We conclude that Nlz1/Znf703 acts as a repressor of transcription and hypothesize that other NET family members function in a similar manner.
锌指蛋白NET亚家族的成员与转录因子Sp家族相关,并且在胚胎发育过程中是必需的。特别是,脊椎动物后脑菱脑节4的形成需要Nlz1/Znf703和Nlz2/Znf503。虽然NET家族蛋白被推测可调节转录,但其作为转录激活因子还是抑制因子仍不清楚。
在此我们证明,Nlz蛋白在细胞系和发育中的斑马鱼胚胎中均抑制转录。我们首先使用基于标准细胞培养的报告基因检测来证明Nlz1/Znf703在四种不同细胞系中抑制荧光素酶报告基因的转录。结构功能分析和药理学抑制进一步揭示,Nlz1介导的抑制作用需要组蛋白去乙酰化酶活性。接下来,我们构建了一个稳定的转基因斑马鱼报告基因系,以证明Nlz1在胚胎发育过程中促进转基因启动子处的组蛋白去乙酰化并抑制转基因表达。最后,通过遗传学方法我们发现,在斑马鱼胚胎发育过程中,内源性Nlz蛋白通过抑制非菱脑节4基因的表达来参与后脑菱脑节4的形成。
我们得出结论,Nlz1/Znf703作为转录抑制因子起作用,并推测其他NET家族成员也以类似方式发挥作用。