set -1介导的H3K4me3修饰调控粗神经孢子虫过氧化氢酶-3的表达。

IF 1.6 4区 生物学 Q3 GENETICS & HEREDITY
Yupeng Zhao, Qun He, Muqun Yu
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引用次数: 0

摘要

清除和适应活性氧(ROS)对细胞存活至关重要。与其他真核生物一样,粗神经孢子虫的过氧化氢酶是负责清除活性氧的主要酶,主要通过分解活性氧的主要类型过氧化氢(h2o2)。它们的表达受到生长和环境条件的严格调控。组蛋白修饰通常与基因转录调控有关。赖氨酸4位点组蛋白H3三甲基化(H3K4me3)是研究最多的组蛋白修饰之一,与转录起始有关。我们发现,在N. crassa中消除H3K4me3导致CAT-3表达水平降低,对h2o2诱导的ROS胁迫的敏感性增加。另一方面,组蛋白甲基转移酶SET-1的过表达导致CAT-3的表达增加。此外,ChIP实验显示,SET-1介导了cat-3 TSS和orf5 '区域的H3K4me3修饰,这调节了RNAPII在cat-3转录中的募集。总之,这些结果表明,组蛋白甲基转移酶COMPASS(与Set1相关的蛋白复合物)复合物介导的H3K4me3在激活猫-3表达中起关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SET-1-mediated H3K4me3 modification regulates catalase-3 expression in Neurospora crassa.

Clearance and adaptation to reactive oxygen species (ROS) are crucial for cell survival. As in other eukaryotes, the catalases in Neurospora crassa are the main enzymes responsible for ROS clearance, primarily by decomposing hydrogen peroxide (H₂O₂), a major type of ROS. Their expression is tightly regulated by growth and environmental conditions. Histone modifications are frequently linked to the regulation of gene transcription. Histone H3 trimethylation at lysine 4 (H3K4me3) is one of the most studied histone modifications and is associated with transcription initiation. We showed that the abolishment of H3K4me3 in N. crassa led to a low CAT-3 expression level and increased sensitivity to H2O2-induced ROS stress. On the other hand, overexpression of the histone methyltransferase SET-1 led to increased expression of CAT-3. Furthermore, ChIP assays revealed that SET-1 mediated H3K4me3 modification at the cat-3 TSS and ORF 5' region, which regulates RNAPII recruitment for cat-3 transcription. Together, these results demonstrate that histone methyltransferase COMPASS (complex of proteins associated with Set1) complex-mediated H3K4me3 plays a key role in activating cat-3 expression in N. crassa.

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来源期刊
Current Genetics
Current Genetics 生物-遗传学
CiteScore
6.00
自引率
0.00%
发文量
34
审稿时长
1 months
期刊介绍: Current Genetics publishes genetic, genomic, molecular and systems-level analysis of eukaryotic and prokaryotic microorganisms and cell organelles. All articles are peer-reviewed. The journal welcomes submissions employing any type of research approach, be it analytical (aiming at a better understanding), applied (aiming at practical applications), synthetic or theoretical. Current Genetics no longer accepts manuscripts describing the genome sequence of mitochondria/chloroplast of a small number of species. Manuscripts covering sequence comparisons and analyses that include a large number of species will still be considered.
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