11. |
- Johansson, Jacob, et al.
(author)
-
An eco-evolutionary model for demographic and phenological responses in migratory birds
- 2012
-
In: BMC Biology. - : MDPI AG. - 1741-7007. ; 1:3, s. 639-657
-
Journal article (peer-reviewed)abstract
- Many migratory birds have changed their timing of arrival at breeding grounds in response to recent climate change. Understanding the adaptive value and the demographic consequences of these shifts are key challenges. To address these questions we extend previous models of phenological adaptation to climate change under territory competition to include feedback from population dynamics, winter survival and habitat productivity. We study effects of improved pre-breeding survival and of earlier food abundance peak. We show that phenological responses depend strongly on equilibrium population density via effects on territory competition. When density is high, improved pre-breeding survival affects selection pressures more than shifts of the resource peak. Under certain conditions, an advanced food peak can even select for later arrival due to competitive release. Improved pre-breeding survival has positive effects on population density that in many cases is stronger than negative effects of an advanced food peak. The fraction of young in the population decreases in all scenarios of change, but food peak shifts only affect population structure marginally unless population density is low. This work thus provides several missing links between phenological adaptation and demographic responses, and augments the toolbox for interpreting ongoing phenological shifts in migratory birds. We illustrate the utility of our model by explaining different patterns in demographic trends and phenological shifts in populations of Pied flycatchers (Ficedula hypoleuca) across Western Europe.
|
|
12. |
- Otto, Thomas D., et al.
(author)
-
A comprehensive evaluation of rodent malaria parasite genomes and gene expression
- 2014
-
In: BMC Biology. - : BioMed Central. - 1741-7007. ; 12
-
Journal article (peer-reviewed)abstract
- BACKGROUND: Rodent malaria parasites (RMP) are used extensively as models of human malaria. Draft RMP genomes have been published for Plasmodium yoelii, P. berghei ANKA (PbA) and P. chabaudi AS (PcAS). Although availability of these genomes made a significant impact on recent malaria research, these genomes were highly fragmented and were annotated with little manual curation. The fragmented nature of the genomes has hampered genome wide analysis of Plasmodium gene regulation and function.RESULTS: We have greatly improved the genome assemblies of PbA and PcAS, newly sequenced the virulent parasite P. yoelii YM genome, sequenced additional RMP isolates/lines and have characterized genotypic diversity within RMP species. We have produced RNA-seq data and utilised it to improve gene-model prediction and to provide quantitative, genome-wide, data on gene expression. Comparison of the RMP genomes with the genome of the human malaria parasite P. falciparum and RNA-seq mapping permitted gene annotation at base-pair resolution. Full-length chromosomal annotation permitted a comprehensive classification of all subtelomeric multigene families including the 'Plasmodium interspersed repeat genes' (pir). Phylogenetic classification of the pir family, combined with pir expression patterns, indicates functional diversification within this family.CONCLUSIONS: Complete RMP genomes, RNA-seq and genotypic diversity data are excellent and important resources for gene-function and post-genomic analyses and to better interrogate Plasmodium biology. Genotypic diversity between P. chabaudi isolates makes this species an excellent parasite to study genotype-phenotype relationships. The improved classification of multigene families will enhance studies on the role of (variant) exported proteins in virulence and immune evasion/modulation.
|
|
13. |
- Sabouri, Nasim, et al.
(author)
-
The essential Schizosaccharomyces pombe Pfh1 DNA helicase promotes fork movement past G-quadruplex motifs to prevent DNA damage
- 2014
-
In: BMC Biology. - : Springer Science and Business Media LLC. - 1741-7007. ; 12:1
-
Journal article (peer-reviewed)abstract
- Background: G-quadruplexes (G4s) are stable non-canonical DNA secondary structures consisting of stacked arrays of four guanines, each held together by Hoogsteen hydrogen bonds. Sequences with the ability to form these structures in vitro, G4 motifs, are found throughout bacterial and eukaryotic genomes. The budding yeast Pif1 DNA helicase, as well as several bacterial Pif1 family helicases, unwind G4 structures robustly in vitro and suppress G4-induced DNA damage in S. cerevisiae in vivo.Results: We determined the genomic distribution and evolutionary conservation of G4 motifs in four fission yeast species and investigated the relationship between G4 motifs and Pfh1, the sole S. pombe Pif1 family helicase. Using chromatin immunoprecipitation combined with deep sequencing, we found that many G4 motifs in the S. pombe genome were associated with Pfh1. Cells depleted of Pfh1 had increased fork pausing and DNA damage near G4 motifs, as indicated by high DNA polymerase occupancy and phosphorylated histone H2A, respectively. In general, G4 motifs were underrepresented in genes. However, Pfh1-associated G4 motifs were located on the transcribed strand of highly transcribed genes significantly more often than expected, suggesting that Pfh1 has a function in replication or transcription at these sites.Conclusions: In the absence of functional Pfh1, unresolved G4 structures cause fork pausing and DNA damage of the sort associated with human tumors.
|
|