TY - JOUR
T1 - Modelling the compartmentalization of splicing factors
AU - Carrero, G.
AU - Hendzel, M. J.
AU - De Vries, G.
N1 - Funding Information:
This research is supported in part by MITACS, a Canadian Network of Centres of Excellence (GC) and the Natural Sciences and Engineering Research Council of Canada (GC and GdeV). MJH is supported by scholarships from the Alberta Heritage Foundation for Medical Research and the Canadian Institutes of Health Research. Project funding was provided by the Alberta Cancer Foundation.
PY - 2006/4/7
Y1 - 2006/4/7
N2 - Splicing factor (SF) compartments, also known as speckles, are heterogeneously distributed compartments within the nucleus of eukaryotic cells that are enriched in pre-mRNA SFs. We derive a fourth-order aggregation- diffusion model that describes a possible mechanism underlying the organization of SFs into speckles. The model incorporates two hypotheses, namely (1) that self-organization of dephosphorylated SFs, modulated by a phosphorylation- dephosphorylation cycle, is responsible for the formation and disappearance of speckles, and (2) that an underlying nuclear structure plays a major role in the organization of SFs. A linear stability analysis about homogeneous steady-state solutions of the model reveals how the self-interaction among dephosphorylated SFs can result in the onset of spatial patterns. A detailed bifurcation analysis of the model describes how phosphorylation and dephosphorylation modulate the onset of the compartmentalization of SFs.
AB - Splicing factor (SF) compartments, also known as speckles, are heterogeneously distributed compartments within the nucleus of eukaryotic cells that are enriched in pre-mRNA SFs. We derive a fourth-order aggregation- diffusion model that describes a possible mechanism underlying the organization of SFs into speckles. The model incorporates two hypotheses, namely (1) that self-organization of dephosphorylated SFs, modulated by a phosphorylation- dephosphorylation cycle, is responsible for the formation and disappearance of speckles, and (2) that an underlying nuclear structure plays a major role in the organization of SFs. A linear stability analysis about homogeneous steady-state solutions of the model reveals how the self-interaction among dephosphorylated SFs can result in the onset of spatial patterns. A detailed bifurcation analysis of the model describes how phosphorylation and dephosphorylation modulate the onset of the compartmentalization of SFs.
KW - Aggregation
KW - Nuclear speckles
KW - Pattern formation
KW - Splicing factors
UR - http://www.scopus.com/inward/record.url?scp=33644892252&partnerID=8YFLogxK
U2 - 10.1016/j.jtbi.2005.07.019
DO - 10.1016/j.jtbi.2005.07.019
M3 - Journal Article
C2 - 16162356
AN - SCOPUS:33644892252
SN - 0022-5193
VL - 239
SP - 298
EP - 312
JO - Journal of Theoretical Biology
JF - Journal of Theoretical Biology
IS - 3
ER -