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1.
Virology ; 488: 169-78, 2016 Jan 15.
Article in English | MEDLINE | ID: mdl-26650692

ABSTRACT

The immune system is able to identify foreign pathogens via different pathways. In the case of viral infection, recognition of the viral RNA is a crucial step, and many efforts have been made to understand which features of viral RNA are detected by the immune system. The biased viral RNA composition, measured as host-virus nucleotidic divergence, or CpG enrichment, has been proposed as salient signal. Peculiar structural features of these RNA could also be related to the immune system activation. Here, we gather multiple datasets and proceed to a meta-analysis to uncover the best predictors of immune system activation by viral RNA. "A" nucleotide content and Minimum Folding Energy are good predictors, and are more easily generalized than more complex indicators suggested previously. As RNA composition and structure are highly correlated, we suggest further experiments on synthetic sequences to identify the viral RNA sensing mechanisms by immune system receptors.


Subject(s)
Immunity, Innate , RNA, Viral/chemistry , RNA, Viral/genetics , Viruses/genetics , Viruses/immunology , Base Composition , Humans , Nucleic Acid Conformation
2.
Oncogene ; 32(22): 2739-46, 2013 May 30.
Article in English | MEDLINE | ID: mdl-22797072

ABSTRACT

Ovarian granulosa cell tumors (OGCT) are the most frequent kind of sex cord-stromal tumors, and represent ∼2-5% of all ovarian malignancies. OGCTs exist as two entities, juvenile and adult types, with specific clinical and pathological characteristics. The molecular pathogenesis of these tumors has just begun to be unraveled. Indeed, recent studies have indicated that mutation and/or misregulation of the key ovarian transcription factor FOXL2 has a role in OGCT formation, although the mechanisms remain unclear. To better understand the molecular characteristics of OGCT, we studied the transcriptomic profiles of ten human adult-type OGCT samples, as well as ethnically matched granulosa cell (GC) controls. We find that the OGCT samples analyzed herein exhibit several hallmarks of cancer, including increased expression of genes linked to cell proliferation, but decreased expression of those conferring sensitivity to cell death. Moreover, genes differentially expressed in OGCTs are significantly enriched for known FOXL2 target genes, consistently with the prevalence of FOXL2 somatic mutation in these tumors. Expression of these targets is altered in a way expected to promote malignant transformation, for instance, through induction of genes associated with faster cell cycling and downregulation of genes associated with cell death. Over time, such defects may be responsible at least partly for the malignant transformation of healthy GCs into OGCT. These insights into the molecular pathogenesis of OGCTs may open the way to new efforts in the development of more targeted therapeutic strategies for OGCT patients.


Subject(s)
Forkhead Transcription Factors/genetics , Granulosa Cell Tumor/genetics , Ovarian Neoplasms/genetics , Adult , Aged , Cell Line, Tumor , Cell Proliferation , Female , Forkhead Box Protein L2 , Gene Expression Profiling , Granulosa Cells/metabolism , Granulosa Cells/pathology , HeLa Cells , Humans , Middle Aged , Mutation , Ovary/pathology , Transcriptome/genetics
3.
Proc Natl Acad Sci U S A ; 108(2): 882-7, 2011 Jan 11.
Article in English | MEDLINE | ID: mdl-21187432

ABSTRACT

External information propagates in the cell mainly through signaling cascades and transcriptional activation, allowing it to react to a wide spectrum of environmental changes. High-throughput experiments identify numerous molecular components of such cascades that may, however, interact through unknown partners. Some of them may be detected using data coming from the integration of a protein-protein interaction network and mRNA expression profiles. This inference problem can be mapped onto the problem of finding appropriate optimal connected subgraphs of a network defined by these datasets. The optimization procedure turns out to be computationally intractable in general. Here we present a new distributed algorithm for this task, inspired from statistical physics, and apply this scheme to alpha factor and drug perturbations data in yeast. We identify the role of the COS8 protein, a member of a gene family of previously unknown function, and validate the results by genetic experiments. The algorithm we present is specially suited for very large datasets, can run in parallel, and can be adapted to other problems in systems biology. On renowned benchmarks it outperforms other algorithms in the field.


Subject(s)
Computational Biology/methods , Signal Transduction/physiology , Adenosine Triphosphatases/chemistry , Algorithms , Alleles , Biophysics/methods , Endosomal Sorting Complexes Required for Transport/chemistry , Models, Biological , Models, Statistical , Pheromones , Plasmids/metabolism , Protein Interaction Mapping , RNA, Messenger/metabolism , Saccharomyces cerevisiae/genetics , Saccharomyces cerevisiae Proteins/chemistry , Software , Transcription, Genetic
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