FP7Индивидуална стипендия2009–2011

OXICELLCYCLE · Coordination of Oxidative Stress Signalling with Forkhead-Regulated Transcription during the Fission Yeast Cell Cycle

7РП — „Хора“ (Действия „Мария Кюри“)

Период
2009-10-01 → 2011-09-30
Финансиране от ЕС
171 868 €
Участници
1
Схема
MC-IEF

Линиите свързват координатора с партньорите.

Накратко на български

Механизмите за репродуктивна изолация между различни диви щамове на дрожди S. pombe се анализират чрез създаване на хибриди и проследяване на оцеляването на спорите им. Това помага на еволюционните биолози да разберат по-добре процесите, чрез които се формират новите видове.

Този кратък обзор е генериран от изкуствен интелект

Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.

Резултати накратко

Coordination of Oxidative Stress Signalling with Forkhead-Regulated Transcription during the Fission Yeast Cell Cycle

This project aimed to characterise with more detail the reproductive isolation mechanism that exist between the different wild isolates of S. pombe. The study of the evolutionary processes responsible for reproductive isolation have been an active field of research in other model organism like Drosophila species and Saccharomyces sensu stricto species (for reviews see [1]), but has only been rarely studied for Schizosaccharomyces species [2]. From the studies carried out in the Saccharomyces sensu stricto species several mechanism responsible for reproductive isolation have been detected in those yeast species [3]. Fission yeast well established model organism and is only distantly related to Saccharomyces genus. On top of that, fission yeast is a haploid organism with a diploid growth only in a transient stage, while Saccharomyces species are often diploids. Altogether this suggest that fission yeast will be a valuable model organism to get more insight into the study of the speciation. The main objective of that project will be to introduce to the research community fission yeast as a powerful organism to study speciation events. This will be relevant for both evolutionary biologist, to get new insights and complement what is already known in the field, and fission yeast community, by introducing evolution as a field of research in the community. In this project we have created a collection of fission yeast diploid hybrids obtained from the crosses of different wild isolates available from microorganism collections all over the world. Sporulation was induced on those diploid hybrids, and spore survival was determined by Random Spore Survival (RSA) or tetrad analysis following protocols described at [4]. Spore survival observed strongly correlates with the degree of sequence variation of the parental strains. Detailed maps of chromosome recombination were obtained for some of the crosses analysed in this study. This study show that while the number of crossover per genome is reduced in crosses involving distantly related strains of S. pombe this is not true when analysing meiosis of diploid hybrids obtained from closely related fission yeast strains. This observation suggest that in fission yeast, as observed in Saccharomyces species and prokaryotic organism [5] [6], mismatch repair proteins could be involved into the reinforcement of reproductive isolation mechanism. Preliminary studies to determine the existence of pairs of Dobzhansky-Muller incompatible alleles have been initiated as result of this project. The analysis by deep sequencing of the proportion of reads originating from both parental strains allowed us to identify candidate regions that show a significant deviation from the expected 2:2 ratio. This finding will allow us to define more concrete research approaches to tackle whether there are incompatibilities between wild isolates of fission yeast that affects the reproductive isolation, and eventually study the molecular mechanism responsible for the incompatibilities observed. 1. Louis, Edward J (2009) 'Evolutionary genetics: Origins of reproductive isolation..' Nature, 457(7229)29th January, pp. 549-550. 2. Kondrat'eva, V I and Naumov, G I (2001) 'The phenomenon of spore killing in Schizosaccharomyces pombe hybrids..' Doklady biological sciences : proceedings of the Academy of Sciences of the USSR, Biological sciences sections / translated from Russian, 379, pp. 385-388. 3. Greig, D (2009) 'Reproductive isolation in Saccharomyces..' Heredity, 102(1), pp. 39-44. 4. Forsburg, Susan L and Rhind, Nicholas (2006) 'Basic methods for fission yeast.' Yeast (Chichester, England), 23(3), pp. 173-183. 5. Hunter, N, Chambers, S R, Louis, E J and Borts, R H (1996) 'The mismatch repair system contributes to meiotic sterility in an interspecific yeast hybrid..' The EMBO Journal, 15(7), pp. 1726-1733. 6. Rayssiguier, C, Thaler, D S and Radman, M (1989) 'The barrier to recombination between Escherichia coli and Salm.

Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз

Цел на проекта

Cellular proliferation and environmental factors in general, and cell cycle-regulated transcription and oxidative stress in particular, are of vital importance for aging and accompanying complex diseases. The overall goal of this project is to gain systems-level insight into the intriguing relationship between oxidative stress signalling and cell cycle regulation. Oxidative stress causes widespread cellular damage by increased concentrations of reactive oxygen species. Available data indicate that specific clusters of cell cycle-regulated genes, whose expression depends on members of the conserved forkhead family of transcription factors, are repressed during oxidative stress, and this repression then promotes cell survival. Using fission yeast as a powerful model system, we plan to use a wide range of genome-wide methodologies combined with genetics to elucidate two major questions regarding the connection between oxidative stress and cell cycle control: 1) how stress-activated signalling pathways regulate forkhead-mediated transcription, and 2) how repression of forkhead-mediated transcription in turn leads to oxidative damage protection. This project, which takes advantage of the use of a simple model organism and multiple high-throughput and integrative approaches, will promote a systems-level understanding of the complex interplay between cell cycle control and oxidative stress signalling. To get the most from the proposed research will require interdisciplinary interactions with colleagues both within the host laboratory and with outside experts. The proposed research should result in valuable fundamental information to help tackle aging-related diseases. Importantly, this fellowship would also provide a rich training opportunity, by diversifying research skills and promoting complementary competencies, which would be a crucial step for the motivated and talented candidate towards an independent research career.

Оригинален текст от CORDIS (на английски).

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Данни: CORDIS, © Европейски съюз