Stonbraker Madison P, DePaul Dominic A, Heidel-Roberts Ethan C, Greene Hallee, Johnson Matthew Logan
Biology Department, University of Pittsburg at Greensburg, Greensburg, Pennsylvania, United States of America.
Open Life Sci. 2025 Aug 20;20(1):20251164. doi: 10.1515/biol-2025-1164. eCollection 2025.
Gene regulation is important during tissue formation, but redundant systems make it difficult to study The protein Jazf-1 is a member of the NuA4/TIP60 histone-modifying complex, and a transcriptional repressor has been suggested to be important for eye development. We used the GAL4-UAS system to determine the impact of altering gene expression. GAL4-UAS manipulations of Jazf-1 in the eye caused variable and not fully penetrant phenotypes. Increased expression of Jazf-1 has been shown to suppress a small eye phenotype. We found that produces a sensitive background for an assay to monitor gene regulatory complexes. Depleting Jazf-1 and other NuA4/TIP60 complex members significantly enhanced the eye phenotype. We also tested Hr78, which directly interacts with Jazf-1, and found it inversely modifies the phenotype. An Hr78 mutation predicted to uncouple the Jazf-1 interaction but still capable of interactions with transcriptional activators further enhanced the mutant phenotype, suggesting the loss of a repressing complex. We believe that Hr78 is acting as an anchor for repressing and activating complexes and the NuA4/TIP60 complex helps repress genes that can negatively impact eye formation in the context of .
基因调控在组织形成过程中很重要,但冗余系统使其难以研究。蛋白质Jazf-1是NuA4/TIP60组蛋白修饰复合体的成员,并且有研究表明一种转录抑制因子对眼睛发育很重要。我们使用GAL4-UAS系统来确定改变基因表达的影响。在眼睛中对Jazf-1进行GAL4-UAS操作会导致可变且不完全显性的表型。已表明Jazf-1表达增加可抑制小眼表型。我们发现[此处原文缺失相关内容]为监测基因调控复合体的检测提供了一个敏感背景。耗尽Jazf-1和其他NuA4/TIP60复合体成员会显著增强眼睛表型。我们还测试了与Jazf-1直接相互作用的Hr78,发现它对[此处原文缺失相关内容]表型有相反的影响。预测会解开Jazf-1相互作用但仍能与转录激活因子相互作用的Hr78突变进一步增强了[此处原文缺失相关内容]突变体表型,表明抑制复合体的丧失。我们认为Hr78作为抑制和激活复合体的锚定物,并且在[此处原文缺失相关内容]的背景下,NuA4/TIP60复合体有助于抑制可能对眼睛形成产生负面影响的基因。