Ref HAL: hal-01939883_v1
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Résumé:

The DNA shows a high degree of spatial and dynamical organization over a broad range of length scales. It interacts with different populations of proteins and can form protein-DNA complexes that underlie various biological processes, including chromosome segregation. A prominent example is the large ParB-DNA complex, an essential component of a widely spread mechanism for DNA segregation in bacteria. Recent studies suggest that DNA-bound ParB proteins interact with each other and condense into large clusters with multiple extruding DNA-loops. In my talk, I present the Looping and Clustering model, a simple statistical physics approach to describe how proteins assemble into a protein-DNA cluster with multiple loops. Our analytic model predicts binding profiles of ParB proteins in good agreement with data from high precision ChIP-sequencing – a biochemical technique to analyze the interaction between DNA and proteins at the level of the genome. The Looping and Clustering framework provides a quantitative tool that could be exploited to interpret further experimental results of ParB-like protein complexes and gain some new insights into the organization of DNA.

Ref HAL: hal-01561696_v1
Ref Arxiv: 1707.01373
DOI: 10.1088/1367-2630/aaad39
WoS: 000428767700002
Ref. & Cit.: NASA ADS
Exporter : BibTex | endNote
4 Citations
Résumé:

The bacterial genome is organized in a structure called the nucleoid by a variety of associated proteins. These proteins can form complexes on DNA that play a central role in various biological processes, including chromosome segregation. A prominent example is the large ParB-DNA complex, which forms an essential component of the segregation machinery in many bacteria. ChIP-Seq experiments show that ParB proteins localize around centromere-like parS sites on the DNA to which ParB binds specifically, and spreads from there over large sections of the chromosome. Recent theoretical and experimental studies suggest that DNA-bound ParB proteins can interact with each other to condense into a coherent 3D complex on the DNA. However, the structural organization of this protein-DNA complex remains unclear, and a predictive quantitative theory for the distribution of ParB proteins on DNA is lacking. Here, we propose the Looping and Clustering (LC) model, which employs a statistical physics approach to describe protein-DNA complexes. The LC model accounts for the extrusion of DNA loops from a cluster of interacting DNA-bound proteins. Conceptually, the structure of the protein-DNA complex is determined by a competition between attractive protein interactions and the configurational and loop entropy of this protein-DNA cluster. Indeed, we show that the protein interaction strength determines the "tightness" of the loopy protein-DNA complex. With this approach we consider the genomic organization of such a protein-DNA cluster around a single high-affinity binding site. Thus, our model provides a theoretical framework to quantitatively compute the binding profiles of ParB-like proteins around a cognate (parS) binding site.

Commentaires: 14 pages, 7 figures

Ref Arxiv: 1101.4908
DOI: 10.1007/JHEP03(2011)138
WoS: 000289295300066
Ref. & Cit.: NASA ADS
40 Citations
Résumé:

We systematically construct a large number of compact Calabi-Yau fourfolds which are suitable for F-theory model building. These elliptically fibered Calabi-Yaus are complete intersections of two hypersurfaces in a six dimensional ambient space. We first construct three-dimensional base manifolds that are hypersurfaces in a toric ambient space. We search for divisors which can support an F-theory GUT. The fourfolds are obtained as elliptic fibrations over these base manifolds. We find that elementary conditions which are motivated by F-theory GUTs lead to strong constraints on the geometry, which significantly reduce the number of suitable models. The complete database of models is available at http://hep.itp.tuwien.ac.at/f-theory/. We work out several examples in more detail.

Commentaires: 35 pages, references added. Réf Journal: JHEP 1103:138,2011

Ref Arxiv: 1108.1394
DOI: 10.1007/JHEP10(2011)091
WoS: 000296917300016
Ref. & Cit.: NASA ADS
5 Citations
Résumé:

Ashok and Douglas have shown that infinite sequences of type IIB flux vacua with imaginary self-dual flux can only occur in so-called D-limits, corresponding to singular points in complex structure moduli space. In this work we refine this no-go result by demonstrating that there are no infinite sequences accumulating to the large complex structure point of a certain class of one-parameter Calabi-Yau manifolds. We perform a similar analysis for conifold points and for the decoupling limit, obtaining identical results. Furthermore, we establish the absence of infinite sequences in a D-limit corresponding to the large complex structure limit of a two-parameter Calabi-Yau. In particular, our results demonstrate analytically that the series of vacua recently discovered by Ahlqvist et al., seemingly accumulating to the large complex structure point, are finite. We perform a numerical study of these series close to the large complex structure point using appropriate approximations for the period functions. This analysis reveals that the series bounce out from the large complex structure point, and that the flux eventually ceases to be imaginary self-dual. Finally, we study D-limits for F-theory compactifications on K3\times K3 for which the finiteness of supersymmetric vacua is already established. We do find infinite sequences of flux vacua which are, however, identified by automorphisms of K3.

Commentaires: 35 pages. v2. Typos corrected, ref. added. Matches published version. Réf Journal: J. High Energy Phys. JHEP10(2011)091