DEVELOP. GENOMICS · Genome organization and transcription at the beginning of development
6РП — Действия „Мария Кюри“
- Период
- 2006-04-01 → 2008-03-31
- Финансиране от ЕС
- 70 100 €
- Участници
- 1
- Схема
- IRG
Линиите свързват координатора с партньорите. За проекти отпреди 2014 г. CORDIS не винаги дава точни координати. Тези точки са на ниво град или държава.
Накратко на български
Геномната организация, например съдържанието на GC-бази в ДНК, влияе върху работата на гени като spdri при ембриони на морски ежици. Това помага да се разбере как химичният състав на генома взаимодейства с регулаторните механизми за управление на генната транскрипция.
Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.
Резултати накратко
Final Activity Report Summary - DEVELOP. GENOMICS (Genome organization and transcription at the beginning of development.)
The purpose of this project was to explore how genomic organisation impacts on regulation of gene transcription, during the early stages of embryonic development. In this research, by genomic organisation is meant variation of GC levels (percentage of Gs and Cs) along the genomic sequence, or composition. This is a convenient choice, given that it can be recognised based on sequence information and that it nicely correlates with several important structural and functional features of genomes. Among these, global levels of gene transcription: on a genome-wide scale, GC-rich genes are embedded in the GC-richer portions of the genome and are transcribed at higher levels than GC-poor ones. On the other hand, it is generally understood that it is the information contained in a gene's cis-regulatory region that determines the time, the place and the amount at which gene transcription happens. Genes' cis-regulatory regions are built in a modular way, each module being a cluster of binding sites for the transcription factors (activators or repressors) that regulate gene expression. Appropriate mRNA production is the result of the integration of the inputs presented at these different binding sites. Therefore, the relationship between composition of genomic context and utilisation of regulatory information is not obvious and it was explored in this work. The experimental system utilised has been the developing sea urchin embryo, a highly accessible model system, whose genetic developmental programming is understood to a good degree. In the course of this research, the regulatory region of the gene spdri, expressed during development of the embryo has been dissected. This information has been utilised to address the main question of this research. The spdri gene is expressed at two different times and places in the developing sea urchin embryo. Two sets of regulatory modules are needed to achieve temporally and spatially correct expression of the gene. In the early as well as in the late expression phase, three different kind of inputs are utilised: positive and globally distributed ones; negative ones (that prevent ectopic expression); positive tissue-specific ones. Composition of spdri's cis-regulatory region matches that of its genomic context. By forcing the incorporation of a trans-gene that contained spdri's cis-regulatory region, in locations of the genome that had a lower or higher GC levels (34 % and 41 % versus 37,9 %), alterations of its expression pattern were observed. Such alterations were never random, as they could be directly related to the loss of function of regulatory modules located at the extremities of spdri's cis-regulatory region. These results indicate that in order to work, a cis-regulatory region needs to be in a compositionally appropriate context. Otherwise, part of the regulatory information remains inaccessible to the transcriptional apparatus. To assess whether these observations refer to some peculiar property of the experimental system chosen or are instead indicative of some more general property, the genomic contexts of 80 human genes were analysed. In all cases, composition of the genomic contexts was found to match that of the cis-regulatory region considered. These results support the idea that gene localisation in genomes is not random and that genomes are integrated ensembles.
Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз
Цел на проекта
We want to address the question of how DNA replication and transcription are coordinated in the early stages developing sea urchin embryo. In this system, even though the embryonic cells are involved in fast-paced cell division transcription begins very early in development. We think that this is possible because the early-stage transcripts constitute a group of GC rich sequences, in the otherwise generally GC-poor and (by vertebrate standard) homogeneous sea urchin genome. This GC richness may be responsible for a positional distribution of these sequences in regions of the genome more readily accessible to the transcriptional apparatus even during fast cycles of chromosomal duplication-condensation.The sea urchin embryo is a system of choice to test this hypothesis because:1) the genome information necessary for the study is (soon to be) available;2) a comprehensive picture of the early development, described in its detailed regulatory gene network circuitries, is being built over the recent years;3) this model system offers great experimental manipulability.The study proposed offers us the opportunity of linking genome organization with transcriptional activity and understanding what the functional relevance of this is in development. The system c hosen provides the ideal portal to understand how the evolutionary process has shaped the genome to make it transcriptionally efficient from the early stages of embryonic life.
Оригинален текст от CORDIS (на английски).
Участници
- STAZIONE ZOOLOGICA ANTON DOHRN" NAPOLI" · NAPOLIКоординаторНиво градИталия
Връзки
Данни: CORDIS, © Европейски съюз
