在果蝇早期发育过程中,两种共同的阴影增强剂调节双生无眼表达。

IF 3.3 3区 生物学 Q2 GENETICS & HEREDITY Genetics Pub Date : 2025-01-08 DOI:10.1093/genetics/iyae176
Jacqueline M Dresch, Luke L Nourie, Regan D Conrad, Lindsay T Carlson, Elizabeth I Tchantouridze, Biruck Tesfaye, Eleanor Verhagen, Mahima Gupta, Diego Borges-Rivera, Robert A Drewell
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引用次数: 0

摘要

无眼果蝇PAX6同源双胞胎位于控制眼睛发育的遗传途径的顶峰,视网膜决定网络。在胚胎中,toy的表达最早可在细胞囊胚第5期被检测到,在假定的头神经外胚层的前-背带中,它产生了视觉系统和大脑的原基。虽然在胚胎中产生位置信息的几个母体转录因子和间隙转录因子与控制玩具有关,但玩具在早期胚胎中的表达调控目前还没有很好的表征。在本研究中,我们采用综合实验方法,利用生物信息学、转基因报告基因检测中假定增强子的分子遗传学检测和早期胚胎中表达模式的定量分析,鉴定了玩具基因上的两个新的协同增强子。此外,我们应用数学模型来剖析玩具的监管景观。我们证明了相对简单的基于热力学的模型,仅包含5个TF结合位点,可以准确地预测2个协同增强子的基因表达,并且HUNCHBACK TF通过激活和抑制的双重功能发挥关键的调节作用。我们的分析还揭示了这两种增强子的分子结构非常不同,这表明它们使用的潜在调控逻辑是不同的。
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Two coacting shadow enhancers regulate twin of eyeless expression during early Drosophila development.

The Drosophila PAX6 homolog twin of eyeless (toy) sits at the pinnacle of the genetic pathway controlling eye development, the retinal determination network. Expression of toy in the embryo is first detectable at cellular blastoderm stage 5 in an anterior-dorsal band in the presumptive procephalic neuroectoderm, which gives rise to the primordia of the visual system and brain. Although several maternal and gap transcription factors that generate positional information in the embryo have been implicated in controlling toy, the regulation of toy expression in the early embryo is currently not well characterized. In this study, we adopt an integrated experimental approach utilizing bioinformatics, molecular genetic testing of putative enhancers in transgenic reporter gene assays and quantitative analysis of expression patterns in the early embryo, to identify 2 novel coacting enhancers at the toy gene. In addition, we apply mathematical modeling to dissect the regulatory landscape for toy. We demonstrate that relatively simple thermodynamic-based models, incorporating only 5 TF binding sites, can accurately predict gene expression from the 2 coacting enhancers and that the HUNCHBACK TF plays a critical regulatory role through a dual-modality function as an activator and repressor. Our analysis also reveals that the molecular architecture of the 2 enhancers is very different, indicating that the underlying regulatory logic they employ is distinct.

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来源期刊
Genetics
Genetics GENETICS & HEREDITY-
CiteScore
6.90
自引率
6.10%
发文量
177
审稿时长
1.5 months
期刊介绍: GENETICS is published by the Genetics Society of America, a scholarly society that seeks to deepen our understanding of the living world by advancing our understanding of genetics. Since 1916, GENETICS has published high-quality, original research presenting novel findings bearing on genetics and genomics. The journal publishes empirical studies of organisms ranging from microbes to humans, as well as theoretical work. While it has an illustrious history, GENETICS has changed along with the communities it serves: it is not your mentor''s journal. The editors make decisions quickly – in around 30 days – without sacrificing the excellence and scholarship for which the journal has long been known. GENETICS is a peer reviewed, peer-edited journal, with an international reach and increasing visibility and impact. All editorial decisions are made through collaboration of at least two editors who are practicing scientists. GENETICS is constantly innovating: expanded types of content include Reviews, Commentary (current issues of interest to geneticists), Perspectives (historical), Primers (to introduce primary literature into the classroom), Toolbox Reviews, plus YeastBook, FlyBook, and WormBook (coming spring 2016). For particularly time-sensitive results, we publish Communications. As part of our mission to serve our communities, we''ve published thematic collections, including Genomic Selection, Multiparental Populations, Mouse Collaborative Cross, and the Genetics of Sex.
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