Vikhyaat Ahlawat, Anshika Dhiman, Hashini Ekanayake Mudiyanselage and Huan-Xiang Zhou*,
{"title":"原胺介导的缠结会产生极度的脱氧核糖核酸压积","authors":"Vikhyaat Ahlawat, Anshika Dhiman, Hashini Ekanayake Mudiyanselage and Huan-Xiang Zhou*, ","doi":"10.1021/jacs.4c1246810.1021/jacs.4c12468","DOIUrl":null,"url":null,"abstract":"<p >In sperm cells, protamine replaces histones to compact DNA 10–20 times more than in somatic cells. To characterize the extreme compaction, we employed confocal microscopy and optical tweezers to determine the conformations and stability of protamine-bound λ-DNA. Confocal images show increasing compaction of λ-DNA at increasing protamine concentration. In the presence of protamine, single λ-DNA molecules form tangles that withstand forces strong enough (∼55 pN) for strand separation and shorten the contour length by up to 40% even at high forces, as well as bends and loops that rupture at 10–40 pN forces. Strand separation nucleates tangles, implicating protamine interactions with DNA bases. Molecular dynamics simulations show that Arg sidechains of protamine each form hydrogen bonds with multiple bases, frequently in the form of a wedge between the two strands of DNA. Protamine may participate in both local and higher-order chromatin organization, leading to extreme compaction and global transcription silencing.</p>","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"146 44","pages":"30668–30677 30668–30677"},"PeriodicalIF":14.4000,"publicationDate":"2024-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Protamine-Mediated Tangles Produce Extreme Deoxyribonucleic Acid Compaction\",\"authors\":\"Vikhyaat Ahlawat, Anshika Dhiman, Hashini Ekanayake Mudiyanselage and Huan-Xiang Zhou*, \",\"doi\":\"10.1021/jacs.4c1246810.1021/jacs.4c12468\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >In sperm cells, protamine replaces histones to compact DNA 10–20 times more than in somatic cells. To characterize the extreme compaction, we employed confocal microscopy and optical tweezers to determine the conformations and stability of protamine-bound λ-DNA. Confocal images show increasing compaction of λ-DNA at increasing protamine concentration. In the presence of protamine, single λ-DNA molecules form tangles that withstand forces strong enough (∼55 pN) for strand separation and shorten the contour length by up to 40% even at high forces, as well as bends and loops that rupture at 10–40 pN forces. Strand separation nucleates tangles, implicating protamine interactions with DNA bases. Molecular dynamics simulations show that Arg sidechains of protamine each form hydrogen bonds with multiple bases, frequently in the form of a wedge between the two strands of DNA. Protamine may participate in both local and higher-order chromatin organization, leading to extreme compaction and global transcription silencing.</p>\",\"PeriodicalId\":49,\"journal\":{\"name\":\"Journal of the American Chemical Society\",\"volume\":\"146 44\",\"pages\":\"30668–30677 30668–30677\"},\"PeriodicalIF\":14.4000,\"publicationDate\":\"2024-10-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the American Chemical Society\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/jacs.4c12468\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/jacs.4c12468","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
在精子细胞中,原胺取代组蛋白压实DNA的程度是体细胞的10-20倍。为了描述这种极端压实的特征,我们使用共聚焦显微镜和光学镊子来确定与原胺结合的λ-DNA的构象和稳定性。共聚焦图像显示,随着原胺浓度的增加,λ-DNA 的压实程度也在增加。在有原胺存在的情况下,单个 λ-DNA 分子会形成缠结,这种缠结能承受足以导致链分离的强力(55 pN),即使在强力下也能将轮廓长度缩短 40%,还能形成在 10-40 pN 的力下断裂的弯曲和环。链分离会导致缠结,这与原胺与 DNA 碱基的相互作用有关。分子动力学模拟显示,原胺的氩侧链分别与多个碱基形成氢键,经常在 DNA 的两条链之间形成楔形。原胺可能参与局部和高阶染色质组织,导致极度压实和全局转录沉默。
Protamine-Mediated Tangles Produce Extreme Deoxyribonucleic Acid Compaction
In sperm cells, protamine replaces histones to compact DNA 10–20 times more than in somatic cells. To characterize the extreme compaction, we employed confocal microscopy and optical tweezers to determine the conformations and stability of protamine-bound λ-DNA. Confocal images show increasing compaction of λ-DNA at increasing protamine concentration. In the presence of protamine, single λ-DNA molecules form tangles that withstand forces strong enough (∼55 pN) for strand separation and shorten the contour length by up to 40% even at high forces, as well as bends and loops that rupture at 10–40 pN forces. Strand separation nucleates tangles, implicating protamine interactions with DNA bases. Molecular dynamics simulations show that Arg sidechains of protamine each form hydrogen bonds with multiple bases, frequently in the form of a wedge between the two strands of DNA. Protamine may participate in both local and higher-order chromatin organization, leading to extreme compaction and global transcription silencing.
期刊介绍:
The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.