EvoBranchingControl2 · Characterisation of the integrative and conserved role of BRC1 in lateral branching control
7РП — „Хора“ (Действия „Мария Кюри“)
- Период
- 2011-10-01 → 2013-09-30
- Финансиране от ЕС
- 166 566 €
- Участници
- 1
- Схема
- MC-IEF
Линиите свързват координатора с партньорите.
Накратко на български
Генът BRC1 контролира страничното разклоняване при растенията, като при картофите неговото изключване води до повече клони и tubers. Разбирането на тези генетични пътища помага за подобряване на характеристиките на важни земеделски култури.
Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.
Резултати накратко
Characterisation of the integrative and conserved role of BRC1 in lateral branching control.
The project “EvoBranchingControl2” aimed to better understand the integrative role of BRANCHED1 (BRC1) in the control of lateral branching in the model species Arabidopsis thaliana by investigating what are the downstream genetic pathways controlled by this transcription factor. In a second time, this project sought to check if in Solanaceae species , specially the tomato species (Solanum lycopersicum) and the potato species (S. tuberosum), which are species are of agronomical interest, the pathways controlled by this gene are conserved. After submitting the project but before getting the results of the FP7 Marie Curie Action we already initiated the first experiments. Because of the highly promising preliminary results we obtained in the potato species we decided to mainly focus the work on this species. In Solanaceae, as a consequence of a whole genome duplication that occurred early after the rise of this family, there are two copies of the ortholog (corresponding gene) AtBRC1 gene called StBRC1a and StBRC1b. The transgenic lines independently inactivating the function of the two genes (RNAinterfering lines) indeed show very interesting phenotype. The StBRC1a- RNAi lines show similar branching phenotype (plants having more banches due to the loss of apical dominance) in the aerial part that its orthologs AtBRC1. Interestingly, these lines also show a branching phenotype at the stolon and tuber level, stolons being also more branched and producing more potatoes than the control lines. The total weight stays however at similar value. At the tuber level, there also is a significant loss of apical dominance of the tube eyes. Most of them are indeed growing in a similar way to the apical eye. Concerning the StBRC1b gene, the corresponding RNAi lines only show weak branching phenotype in either aerial or subterranean level. But they show thicker plant sometimes having aerial tubers. Theses lines produce the similar number of tubers compared to the wild type and control lines but significantly slightly thicker. This could mean this gene is following a neo-functionalization process thus acquiring a new function related to the control of the tuberization process. In a consistent manner, the transgenic lines overexpressing one of these two genes show the opposite phenotype. We also generated transgenic plants inactivating the two genes in the same time to check out if we can get more and bigger potatoes in this way. During these two years we thus further characterized these two genes, investigating what are their role and their regulation. We specially focused on the role of the gene StBRC1b that has a new function in a phenomenon (tuberization) of first interest in the agricultural point of view. We could show the two genes are highly connected, the expression of the two being inter-dependent. These two genes also respond to different factors like endogenous ones like hormones (Auxin, Cytokinin, Gibberellin) or environmental like shadow and darkness. We also showed these two genes are interacting with the gene called SP6A that is considered as one of the key gene involved in the tuberization process (Navarro C. et al., Nature 2011). At the protein level, by using different technics like two hybrid assay or Bimolecular Fluorescence Complementation (BiFC) method in confocal microscopy we showed the twoBRC1 genes are also highly connected as well as with the gene SP6A. We also showed that the protein BRC1a as particular system of regulation of its function at the cellular level. Indeed, an alternative splicing of this gene generate an second protein that has a cytoplasmic localization and preventing the normal version of the protein to go to the nucleus to accomplish its function of transcription factor. In summary, this project allowed doing first characterization at the genetic an protein levels of two copies of the transcription factor BRC1 involved in two important processes of the potato species development that are the control of the plant architecture as well the control of tuberization. More than its importance at the scientific and academic level, because potatoe plants are also important for human and animal feeding, this work may have an important economical role achieving in this way the goal of the Marie Curie Action.
Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз
Цел на проекта
Control of branching is a major determinant for the vast diversity of plant shoot system architectures. After initiation, axillary meristems develop into axillary buds. Branching patterns depend on a key developmental decision: whether axillary buds grow out to give a branch or come in a reversible dormancy statement remaining small in the axils of leaves. This decision is controlled by different developmental or environmental stimuli (apical dominance, photoperiod, shade avoidance syndrome, etc…) which are perceived in different regions of the plant and transduced into the axillary buds to be translated into a local response of growth arrest or stimulation in order to adapt to changing conditions. The molecular mechanisms of integration of these stimuli as well as dormancy control remain fairly unknown. Recently the laboratory of P. Cubas, the host laboratory, characterised the TCP gene BRANCHED1 (BRC1) as a key regulator of branching control in Arabidopsis thaliana. This function interestingly seems to be conserved in Angiosperm.We first plan to do ChIP-SEQ experiment and compare the results obtained with those obtained from microarray analyses comparing genes expression between wild type A. thaliana axillary buds and BRC1 RNAi line or inducible BRC1 line. This seeks to isolate the target genes of BRC1 which should play a role in control of meristem dormancy. We then plan to test the conservative role of BRC1 orthologs in two Solanaceae species (S. lycopersicum and S. tuberosum) by producing RNAi lines.This is an original project based on standard genetic techniques (RNAi, one yeast hybrid) as well as cutting edge genomics technique (ChIP-SEQ) which addresses questions from highly competitive research fields which are meristem development, apical dominance, shade avoidance syndrome, etc…
Оригинален текст от CORDIS (на английски).
Участници
- AGENCIA ESTATAL CONSEJO SUPERIOR DE INVESTIGACIONES CIENTIFICAS · MadridКоординаторИспания
Връзки
Данни: CORDIS, © Европейски съюз
