HJMIGRA · Single-molecule analysis of Holliday-junction (HJ) migration by the human double-HJ dissolvasome
„Хоризонт 2020“ — Действия „Мария Склодовска-Кюри“
- Период
- 2015-05-01 → 2017-04-30
- Финансиране от ЕС
- 146 239 €
- Участници
- 1
- Схема
- MSCA-IF-EF-RI
Линиите свързват координатора с партньорите.
Накратко на български
Молекулярните механизми на протеиновия комплекс „дизолвазом“ при разплитането на специфични ДНК структури се анализират с помощта на специален микроскоп. Това помага за разбирането на процесите по поправка на ДНК, които предпазват клетките от ракови трансформации.
Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.
Резултати накратко
Single-molecule analysis of Holliday-junction (HJ) migration by the human double-HJ dissolvasome
The project objective was to investigate the molecular mechanisms of the critical final steps of homologous recombination (HR) based DNA repair. HR enables the cells to maintain genome integrity as a prerequisite for avoiding cancerous transformations. One important pathway of HR is the double-stranded DNA break repair (DSBR) that employs an enzyme complex (‘dissolvasome’) to dissolve the formed double Holliday junction (DHJ) intermediate structure in a solely non-crossover manner, which thereby helps to maintain chromosome integrity. Although the key proteins in the dissolution reaction have been described, the precise molecular mechanism of HJ migration has not been clarified in details, yet. One major aim of the project aimed to design and purify a mobile HJ substrate and follow dissolvasome mediated branch migration at the single molecule level. Thus, we setup a multichannel detection total internal reflection fluorescence (TIRF) microscope combined with microfluidic flow-cells. This helps us to elucidate the molecular events during HJ migration and the roles of the complex components in this important biological process.
Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз
Цел на проекта
The project outlined here investigates the molecular mechanisms of the critical final steps of homologous recombination (HR) based DNA repair, a pathway that supports the error-free repair of double-stranded DNA breaks (DSBs). In HR, the broken DNA ends are processed and homologous DNA provides a template for repair. Engagement of both processed ends leads to the formation of a double Holliday-junction (DHJ) structure. DHJ can be resolved by enzymatic cleavage or dissolved by the concerted action of a specialized group of helicases (RecQ-family helicases including Bloom’s syndrome helicase (BLM)) and Type I topoisomerases (e.g. TOP3A). In humans the ‘dissolvasome complex’ consists of BLM, TOP3A and regulatory proteins (RMI1, RMI2), called the BTR complex. The BTR complex dissolves DHJ by 1. convergent branch migration of the two independent HJs and 2. decatenation of the final hemicatenate structure. Thus, dissolution solely results non-crossover products, which is necessary to avoid chromosomal rearrangements. What is the mechanism of HJ migration? What are the exact roles of the subunits of the BTR complex? How long can a HJ migrate (i.e. how processive is the ‘dissolvasome’)? How specific is the DHJ migration to the BTR complex compared to other human RecQ helicases? Here we aim to address these questions by using state-of-the-art single-molecule and solution biophysical and biochemical techniques. We will generate a previously inaccessible mobile HJ substrate integrated into λ-bacteriophage DNA. We will follow the processes underlying HJ migration by fluorescently labeling the BTR complex, HJ position and DNA end in total internal reflection fluorescence (TIRF) microscopy combined with microfluidics. Elucidation of the detailed roles of the BTR components in HJ branch migration will help us to understand their roles in genome maintenance.
Оригинален текст от CORDIS (на английски).
Участници
- EOTVOS LORAND TUDOMANYEGYETEM · BudapestКоординаторУнгария
Връзки
Данни: CORDIS, © Европейски съюз