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Найдено документов в текущей БД: 2

    Dynamical modeling of microRNA action on the protein translation process
[Text] / A.Zinovyev [et al.] // BMC Syst. Biol. - 2010. - Vol. 4. - Ст. 13, DOI 10.1186/1752-0509-4-13. - Cited References: 66. - We acknowledge support from Agence Nationale de la Recherche (project ANR-08-SYSC-003 CALAMAR) and from the Projet Incitatif Collaboratif "Bioinformatics and Biostatistics of Cancer" at Institut Curie. AZ and EB are members of the team "Systems Biology of Cancer" Equipe labellis'ee par la Ligue Nationale Contre le Cancer. This work was supported by the European Commission Sixth Framework Programme Integrated Project SIROCCO contract number LSHG-CT-2006-037900. We thank Vitaly Volpert and Laurence Calzone for inspiring and useful discussions. . - ISSN 1752-0509
РУБ Mathematical & Computational Biology

Аннотация: Background: Protein translation is a multistep process which can be represented as a cascade of biochemical reactions (initiation, ribosome assembly, elongation, etc.), the rate of which can be regulated by small non-coding microRNAs through multiple mechanisms. It remains unclear what mechanisms of microRNA action are the most dominant: moreover, many experimental reports deliver controversial messages on what is the concrete mechanism actually observed in the experiment. Nissan and Parker have recently demonstrated that it might be impossible to distinguish alternative biological hypotheses using the steady state data on the rate of protein synthesis. For their analysis they used two simple kinetic models of protein translation. Results: In contrary to the study by Nissan and Parker, we show that dynamical data allow discriminating some of the mechanisms of microRNA action. We demonstrate this using the same models as developed by Nissan and Parker for the sake of comparison but the methods developed (asymptotology of biochemical networks) can be used for other models. We formulate a hypothesis that the effect of microRNA action is measurable and observable only if it affects the dominant system (generalization of the limiting step notion for complex networks) of the protein translation machinery. The dominant system can vary in different experimental conditions that can partially explain the existing controversy of some of the experimental data. Conclusions: Our analysis of the transient protein translation dynamics shows that it gives enough information to verify or reject a hypothesis about a particular molecular mechanism of microRNA action on protein translation. For multiscale systems only that action of microRNA is distinguishable which affects the parameters of dominant system (critical parameters), or changes the dominant system itself. Dominant systems generalize and further develop the old and very popular idea of limiting step. Algorithms for identifying dominant systems in multiscale kinetic models are straightforward but not trivial and depend only on the ordering of the model parameters but not on their concrete values. Asymptotic approach to kinetic models allows putting in order diverse experimental observations in complex situations when many alternative hypotheses co-exist.


Доп.точки доступа:
Zinovyev, A.; Morozova, N.; Nonne, N.; Barillot, E.; Harel-Bellan, A.; Gorban, A.N.; Горбань, Александр Николаевич

    Amazing symmetrical clustering in chloroplast genomes
/ M. G. Sadovsky, M. Y. Senashova, A. V. Malyshev // BMC Bioinformatics. - 2020. - Vol. 21. - Ст. 83, DOI 10.1186/s12859-020-3350-z. - Cited References:45 . - ISSN 1471-2105
РУБ Biochemical Research Methods + Biotechnology & Applied Microbiology
Рубрики:
PHYLOGENETIC ANALYSIS
   DNA

   EVOLUTION

   SYSTEMATICS

   MANIFOLDS

   BACTERIA

Кл.слова (ненормированные):
Order -- Triplet -- Clustering

Аннотация: Background Previously, a seven-cluster pattern claiming to be a universal one in bacterial genomes has been reported. Keeping in mind the most popular theory of chloroplast origin, we checked whether a similar pattern is observed in chloroplast genomes. Results Surprisingly, eight cluster structure has been found, for chloroplasts. The pattern observed for chloroplasts differs rather significantly, from bacterial one, and from that latter observed for cyanobacteria. The structure is provided by clustering of the fragments of equal length isolated within a genome so that each fragment is converted in triplet frequency dictionary with non-overlapping triplets with no gaps in frame tiling. The points in 63-dimensional space were clustered due to elastic map technique. The eight cluster found in chloroplasts comprises the fragments of a genome bearing tRNA genes and exhibiting excessively high GC-content, in comparison to the entire genome. Conclusion Chloroplasts exhibit very specific symmetry type in distribution of coding and non-coding fragments of a genome in the space of triplet frequencies: this is mirror symmetry. Cyanobacteria may have both mirror symmetry, and the rotational symmetry typical for other bacteria.

WOS

Держатели документа:
RAS, SB, Inst Computat Modelling, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Svobodny Prosp 79, Krasnoyarsk 660041, Russia.
VF Voino Yasenetsky Krasnoyarsk State Med Univ, P Zheleznjaka Str 1, Krasnoyarsk 660022, Russia.

Доп.точки доступа:
Sadovsky, Michael G.; Senashova, Maria Yu; Malyshev, Andrew V.