Trapping of yFACT at 3' ends of genes is not a universal characteristic of yeast versions of Bryant-Li-Bhoj syndrome histone H3 mutants.

microPublication biology Pub Date : 2024-10-25 eCollection Date: 2024-01-01 DOI:10.17912/micropub.biology.001384
Joseph S Beard, Lillian K Francis, Reece C Forrest, Agustin Kalinowski, Jackson C Parks, William H Griffin, Caroline L Tackett, Andrea A Duina
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Abstract

Bryant-Li-Bhoj syndrome (BLBS) is associated with germline mutations in the genes encoding human histone H3.3. While to date 70 H3.3 mutants have been associated with BLBS, the molecular mechanisms underpinning this condition remain undefined. We recently showed that in yeast the H3-L61R BLBS mutant causes trapping of yFACT at 3' ends of genes, raising the possibility that this defect could be a contributing factor to disease across all H3-BLBS mutants. Here, we show that of nine additional yeast H3-BLBS mutants analyzed, only one causes yFACT 3' end-trapping, thus indicating that this defect is not a universal feature of H3-BLBS mutants. We also present additional phenotypic data that could provide insights into the molecular mechanisms contributing to BLBS in human patients.

在基因 3' 端捕获 yFACT 并不是布赖恩特-李-波杰综合征组蛋白 H3 突变体酵母版本的普遍特征。
布赖恩特-李-博伊综合征(Bryant-Li-Bhoj Syndrome,BLBS)与编码人类组蛋白 H3.3 的基因的种系突变有关。迄今为止,已有 70 个 H3.3 突变体与 BLBS 有关,但这种病症的分子机制仍未确定。我们最近发现,在酵母中,H3-L61R BLBS 突变体会导致 yFACT 在基因的 3' 端被捕获,这就提出了一个可能性,即这一缺陷可能是所有 H3-BLBS 突变体致病的一个因素。在这里,我们发现在所分析的另外九个酵母 H3-BLBS 突变体中,只有一个会导致 yFACT 3' 末端捕获,从而表明这一缺陷并不是 H3-BLBS 突变体的普遍特征。我们还提供了更多表型数据,这些数据可以帮助我们深入了解导致人类患者 BLBS 的分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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