Department of Biological Sciences, Clemson University, Clemson, SC, USA.
Technical Research Centre, S.N. Bose National Centre for Basic Sciences, Kolkata, WB, India.
J Hazard Mater. 2024 Dec 5;480:135845. doi: 10.1016/j.jhazmat.2024.135845. Epub 2024 Sep 16.
3,3',5.5'-Tetrabromobisphenol A (TBBPA) is a widely used brominated flame-retardant. The objective of this study is to use zebrafish as a model and determine the effects of TBBPA exposure on early embryogenesis. We initiated TBBPA exposures at 0.75 h post fertilization (hpf) and showed that TBBPA induced developmental delays during maternal-to-zygotic transition (MZT) and zygotic genome activation (ZGA). To examine the genetic basis of TBBPA-induced delays, we conducted mRNA-sequencing on embryos exposed to 0 or 40 μM TBBPA from 0.75 hpf to 2, 3.5 or 4.5 hpf. Read count data showed that while TBBPA exposures had no overall impacts on maternal or maternal-zygotic genes, collective read counts for zygotically activated genes were lower in TBBPA treatment at 4.5 hpf compared to time-matched controls, suggesting that TBBPA delays ZGA. Gene ontology assessments for both time- and stage-matched differentially expressed genes revealed TBBPA-induced inhibition of chromatin assembly- a process regulated by histone modifications. Immunostaining and in vitro experiments showed inhibition of histone H3 lysine 27 acetylation (H3K27Ac) as well as its catalyzing enzyme, p300. Finally, co-exposure with a p300 activator showed partial mitigation of effects, demonstrating that inhibition of histone acetylation drives TBBPA-induced developmental delays.
四溴双酚 A(TBBPA)是一种广泛使用的溴化阻燃剂。本研究旨在以斑马鱼为模型,确定 TBBPA 暴露对早期胚胎发生的影响。我们在受精后 0.75 小时(hpf)开始 TBBPA 暴露,并表明 TBBPA 在母体到合子过渡(MZT)和合子基因组激活(ZGA)期间诱导发育延迟。为了研究 TBBPA 诱导延迟的遗传基础,我们对暴露于 0 或 40 μM TBBPA 的胚胎进行了 mRNA 测序,从 0.75 hpf 到 2、3.5 或 4.5 hpf。读取计数数据表明,尽管 TBBPA 暴露对母体或母体-合子基因没有总体影响,但在 4.5 hpf 时,TBBPA 处理中合子激活基因的总读取计数低于时间匹配对照,表明 TBBPA 延迟 ZGA。针对时间和阶段匹配的差异表达基因的基因本体评估显示,TBBPA 诱导了染色质组装的抑制 - 这一过程受组蛋白修饰调节。免疫染色和体外实验表明,组蛋白 H3 赖氨酸 27 乙酰化(H3K27Ac)及其催化酶 p300 的抑制。最后,与 p300 激活剂的共同暴露显示出部分缓解作用,表明组蛋白乙酰化的抑制导致 TBBPA 诱导的发育延迟。