Zelda is dispensable for Drosophila melanogaster histone gene regulation.

IF 3.1 3区 生物学 Q3 CELL BIOLOGY Molecular Biology of the Cell Pub Date : 2025-02-01 Epub Date: 2024-12-11 DOI:10.1091/mbc.E24-01-0028
Tommy O'Haren, Tsutomu Aoki, Leila E Rieder
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Abstract

To ensure that the embryo can package exponentially increasing amounts of DNA, replication-dependent histones are some of the earliest transcribed genes from the zygotic genome. However, how the histone genes are identified is not known. The Drosophila melanogaster pioneer factor CLAMP regulates the embryonic histone genes and helps establish the histone locus body, a suite of factors that controls histone mRNA biosynthesis, but CLAMP is not unique to the histone genes. Zelda collaborates with CLAMP across the genome to regulate zygotic genome activation and target early activated genes. We hypothesized that Zelda helps identify histone genes for early embryonic expression. We found that Zelda targets the histone gene locus early during embryogenesis, prior to histone gene expression. However, depletion of zelda in the early embryo does not affect histone mRNA levels or prevent the recruitment of other factors. These results suggest the earliest events responsible for specifying the zygotic histone genes remain undiscovered.

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Zelda对黑腹果蝇组蛋白基因调控是不可或缺的。
为了确保胚胎能够包装呈指数增长的DNA,复制依赖性组蛋白是从合子基因组中最早转录的基因之一。然而,如何鉴定组蛋白基因尚不清楚。果蝇黑腹鼠先导因子CLAMP调节胚胎组蛋白基因并帮助建立组蛋白位点体,这是一套控制组蛋白mRNA生物合成的因子,但CLAMP并不是组蛋白基因所独有的。Zelda与整个基因组的CLAMP合作,调节受精卵基因组的激活,并针对早期激活的基因。我们假设Zelda有助于识别早期胚胎表达的组蛋白基因。我们发现Zelda在胚胎发生早期靶向组蛋白基因位点,早于组蛋白基因表达。然而,早期胚胎中zelda的缺失并不影响组蛋白mRNA水平或阻止其他因子的募集。这些结果表明,最早的事件负责指定合子组蛋白基因仍未被发现。
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来源期刊
Molecular Biology of the Cell
Molecular Biology of the Cell 生物-细胞生物学
CiteScore
6.00
自引率
6.10%
发文量
402
审稿时长
2 months
期刊介绍: MBoC publishes research articles that present conceptual advances of broad interest and significance within all areas of cell, molecular, and developmental biology. We welcome manuscripts that describe advances with applications across topics including but not limited to: cell growth and division; nuclear and cytoskeletal processes; membrane trafficking and autophagy; organelle biology; quantitative cell biology; physical cell biology and mechanobiology; cell signaling; stem cell biology and development; cancer biology; cellular immunology and microbial pathogenesis; cellular neurobiology; prokaryotic cell biology; and cell biology of disease.
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