Ostalé Cristina M, Azpiazu Natalia, Peropadre Ana, Martín Mercedes, Ruiz-Losada Mireya, López-Varea Ana, Viales Rebecca R, Girardot Charles, Furlong Eileen E M, de Celis Jose F
Centro de Biología Molecular 'Severo Ochoa', Department of Tissue and Organ Homeostasis, CSIC and Universidad Autónoma de Madrid, Madrid 28049, Spain.
Department of Biology, Universidad Autónoma de Madrid, Madrid 28049, Spain.
Development. 2025 May 15;152(10). doi: 10.1242/dev.204258. Epub 2025 May 16.
The conserved Spalt proteins regulate gene expression and cell fate choices during multicellular development, generally acting as transcriptional repressors in different gene regulatory networks. In addition to their roles as DNA sequence-specific transcription factors, Spalt proteins show a consistent localization to heterochromatic regions. Vertebrate Spalt-like proteins can act through the nucleosome remodeling and deacetylase complex to promote closing of open chromatin domains, but their activities also rely on interactions with DNA methyltransferases or with the lysine-specific histone demethylase LSD1, suggesting that they participate in multiple regulatory mechanisms. Here, we describe several consequences of loss of Spalt function in Drosophila cells, including changes in chromatin accessibility, generation of DNA damage, alterations in the localization of chromosomes within the nucleus in the salivary glands and misexpression of transposable elements. We suggest that these effects are related to roles of Spalt proteins in the regulation of heterochromatin formation and chromatin organization. We propose that Drosophila Spalt proteins have two complementary functions, acting as sequence-specific transcriptional repressors on specific target genes and regulating more global gene silencing through the generation or maintenance of heterochromatic domains.
保守的Spalt蛋白在多细胞发育过程中调节基因表达和细胞命运选择,通常在不同的基因调控网络中作为转录抑制因子发挥作用。除了作为DNA序列特异性转录因子的作用外,Spalt蛋白在异染色质区域表现出一致的定位。脊椎动物的Spalt样蛋白可以通过核小体重塑和去乙酰化酶复合物发挥作用,以促进开放染色质结构域的关闭,但其活性也依赖于与DNA甲基转移酶或赖氨酸特异性组蛋白去甲基化酶LSD1的相互作用,这表明它们参与多种调控机制。在这里,我们描述了果蝇细胞中Spalt功能丧失的几个后果,包括染色质可及性的变化、DNA损伤的产生、唾液腺细胞核内染色体定位的改变以及转座元件的错误表达。我们认为这些效应与Spalt蛋白在异染色质形成和染色质组织调控中的作用有关。我们提出果蝇Spalt蛋白具有两种互补功能,作为特定靶基因上的序列特异性转录抑制因子,并通过异染色质结构域的产生或维持来调节更广泛的基因沉默。