Cryo-H-Rec · Cryo-EM Imaging of Histone Recycling at the Replication Fork
„Хоризонт 2020“ — Действия „Мария Склодовска-Кюри“
- Период
- 2019-04-01 → 2021-03-31
- Финансиране от ЕС
- 212 934 €
- Участници
- 1
- Схема
- MSCA-IF-EF-ST
Линиите свързват координатора с партньорите.
Накратко на български
Хистоните са протеини, които опаковат ДНК и носят епигенетични марки, определящи кои гени да се активират. Разбирането на начина, по който тези марки се предават при копирането на ДНК, помага при изследването на рак, диабет и сърдечни проблеми.
Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.
Резултати накратко
Cryo-EM Imaging of Histone Recycling at the Replication Fork
Epigenetics involves all mechanisms of biological inheritance that do not include changes in DNA sequence. It has been implicated in regular developmental processes like cell differentiation, as well as in pathological processes like cancers and psychological disorders. One of the major mechanisms of epigenetic inheritance is through histone modifications. Histones are proteins responsible for tight packing of DNA into small units called nucleosomes. Histone tails extend beyond nucleosomes and they are susceptible to certain modifications that represent epigenetic marks. In turn, these marks signal whether a gene where they are located is going to be expressed or not. Therefore, it is of utmost importance that epigenetic marks are maintained during DNA replication. As replication machinery proceeds along DNA, it needs to disassemble tightly packed histone-DNA units (nucleosomes) in order to access DNA and duplicate it. These histones in front of the replication machinery are called parental histones. However, replication machinery also needs to keep disassembled parental histones with their particular epigenetic marks close by, and to hand them over to two newly duplicated DNA (labelled as leading and lagging strand) where they are subsequently assembled into new nucleosomes. In this way, two duplicated DNA molecules will keep the same epigenetic marks as the original DNA molecule. The main objective of this project is to unravel how replication machinery disassembles nucleosome, how it keeps parental histones close by and how it hands them over to two newly duplicated DNA strands. Epigenetic inheritance is of significant importance for wider society, as it is involved in widespread medical conditions like behavioural disorders, cancers, diabetes and heart problems, as well as in ageing. Understanding molecular mechanism of epigenetic inheritance is required for development of epigenetic therapies that have already shown potential in treatments of certain cancers. This project has shed some valuable light on the previously unknown mechanism of parental histone recycling. It identified key components of the replication machinery that are responsible for keeping parental histones by its side and offered clues for understanding how they are subsequently handed over behind the replication machinery, towards new DNA strands.
Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз
Цел на проекта
DNA replication is essential for cell proliferation. In eukaryotic cells, DNA is densely packaged in nucleosome arrays that form chromatin. Such organisation protects the genetic material and controls access to DNA, thus providing an important mechanism for regulating gene expression. The eukaryotic replication machinery has evolved to unravel nucleosomes in order to access and duplicate DNA, while also maintaining chromatin density on newly duplicated DNA. To achieve this, the replisome dismantles nucleosomes ahead of the replication fork and reassembles them on nascent DNA strands, by coordinating redeposition of parental and newly synthesized histones. Histone proteins are subject to an array of post-translational modifications (PTMs), providing an epigenetic code that modulates activation and silencing of specific chromosomal regions. Redeposition of parental histones with their PTMs on both nascent DNA strands is, thus, pivotal in transmission of the epigenetic marks to daughter cells. I intend to perform in vitro reconstitution of the replisome on a chromatinised template and use cryo-electron microscopy to image DNA duplication and parental histone recycling at the replication fork. I seek to describe different structural intermediates in the process of nucleosome disassembly, DNA duplication and histone incorporation into new nucleosomes. To capture and characterise intermediate states of the replication machinery during this concerted process, I will employ a multidisciplinary approach and resort to structural techniques complementary to cryo-EM like solution NMR spectroscopy and crosslinking-mass spectrometry (XL-MS). My results will help dissect the role of different replisome components in nucleosome reshuffling at the replication fork, and elucidate the molecular mechanism that underpins chromosome replication and epigenetic inheritance.
Оригинален текст от CORDIS (на английски).
Участници
- THE FRANCIS CRICK INSTITUTE LIMITED · LondonКоординаторОбединеното кралство
Връзки
Данни: CORDIS, © Европейски съюз
