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配子体发育过程中独特的组蛋白翻译后修饰。

Distinct Histone Post-translational Modifications during Gametocyte Development.

机构信息

Department of Internal Medicine, Morsani College of Medicine, University of South Florida, 3720 Spectrum Blvd, Tampa, Florida 33612, United States.

Center for Global Health and Infectious Diseases Research, College of Public Health, University of South Florida, 3720 Spectrum Blvd, Tampa, Florida 33612, United States.

出版信息

J Proteome Res. 2022 Aug 5;21(8):1857-1867. doi: 10.1021/acs.jproteome.2c00108. Epub 2022 Jun 30.

DOI:10.1021/acs.jproteome.2c00108
PMID:35772009
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9738646/
Abstract

Histones are the building units of nucleosomes, which constitute chromatin. Histone post-translational modifications (PTMs) play an essential role in epigenetic gene regulation. The genome encodes canonical and variant histones and a collection of conserved enzymes for histone PTMs and chromatin remodeling. Herein, we profiled the histone PTMs during the development of gametocytes, the obligatory stage for parasite transmission. Mass spectrometric analysis of histones extracted from the early, middle, and late stages of gametocytes identified 457 unique histone peptides with 90 PTMs, of which 50% were novel. The gametocyte histone PTMs display distinct patterns from asexual stages, with many new methylation sites in histones H3 and H3.3 (, K14, K18, and K37). Quantitative analyses revealed a high abundance of acetylation in H3 and H4, mono-methylation of H3/H3.3 K37, and ubiquitination of H3BK112, suggesting that these PTMs play critical roles in gametocytes. Gametocyte histones also showed extensive and unique combinations of PTMs. These data indicate that the parasite harbors distinct transcription regulation mechanisms during gametocyte development and lay the foundation for further characterization of epigenetic regulation in the life cycle of the malaria parasite.

摘要

组蛋白是核小体的构建单元,核小体构成染色质。组蛋白的翻译后修饰(PTMs)在表观遗传基因调控中起着至关重要的作用。基因组编码经典和变体组蛋白以及一组用于组蛋白 PTM 和染色质重塑的保守酶。在此,我们对配子体发育过程中的组蛋白 PTM 进行了分析,配子体是寄生虫传播的必需阶段。从配子体的早期、中期和晚期提取的组蛋白的质谱分析鉴定出 457 个独特的组蛋白肽段,具有 90 种 PTM,其中 50%是新的。配子体组蛋白 PTM 与无性阶段显示出不同的模式,在组蛋白 H3 和 H3.3(、K14、K18 和 K37)中有许多新的甲基化位点。定量分析显示 H3 和 H4 中的乙酰化水平很高,H3/H3.3 K37 的单甲基化和 H3BK112 的泛素化,表明这些 PTM 在配子体中发挥着关键作用。配子体组蛋白还显示出广泛而独特的 PTM 组合。这些数据表明寄生虫在配子体发育过程中具有独特的转录调控机制,并为进一步研究疟原虫生命周期中的表观遗传调控奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5619/9738646/323911bb808d/nihms-1854568-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5619/9738646/6f1785e61a58/nihms-1854568-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5619/9738646/4c55d69a9809/nihms-1854568-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5619/9738646/81f85cff1340/nihms-1854568-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5619/9738646/323911bb808d/nihms-1854568-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5619/9738646/6f1785e61a58/nihms-1854568-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5619/9738646/4c55d69a9809/nihms-1854568-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5619/9738646/81f85cff1340/nihms-1854568-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5619/9738646/323911bb808d/nihms-1854568-f0005.jpg

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