Potyviral VPg enhances viral RNA Translation and inhibits reporter mRNA translation in planta

Viral protein genome-linked (VPg) plays a central role in several stages of potyvirus infection. This study sought to answer questions about the role of Potato virus A (PVA; genus Potyvirus) VPg in viral and host RNA expression. When expressed in Nicotiana benthamiana leaves in trans, a dual role of VPg in translation is observed. It repressed the expression of monocistronic luciferase (luc) mRNA and simultaneously induced a significant upregulation in the expression of both replicating and nonreplicating PVA RNAs. This enhanced viral gene expression was due at least to the 5' untranslated region (UTR) of PVA RNA, eukaryotic initiation factors 4E and iso 4E [eIF4E/eIF(iso)4E], and the presence of a sufficient amount of VPg. Coexpression of VPg with viral RNA increased the viral RNA amount, which was not the case with the monocistronic mRNA. Both mutations at certain lysine residues in PVA VPg and eIF4E/eIF(iso)4E depletion reduced its ability to upregulate the viral RNA expression. These modifications were also involved in VPg-mediated downregulation of monocistronic luc expression. These results suggest that VPg can titrate eIF4Es from capped monocistronic RNAs. Because VPg-mediated enhancement of viral gene expression required eIF4Es, it is possible that VPg directs eIF4Es to promote viral RNA expression. From this study it is evident that VPg can serve as a specific regulator of PVA expression by boosting the viral RNA amounts as well as the accumulation of viral translation products. Such a mechanism could function to protect viral RNA from being degraded and to secure efficient production of coat protein (CP) for virion formation.     

Structural flexibility allows the functional diversity of potyvirus genome-linked protein VPg

Several viral genome-linked proteins (VPgs) of plant viruses are intrinsically disordered and undergo folding transitions in the presence of partners. This property has been postulated to be one of the factors that enable the functional diversity of the protein. We created a homology model of Potato virus A VPg and positioned the known functions and structural properties of potyviral VPgs on the novel structural model. The model suggests an elongated structure with a hydrophobic core composed of antiparallel β-sheets surrounded by helices and a positively charged contact surface where most of the known activities are localized. The model most probably represents the fold induced immediately after binding of VPg to a negatively charged lipid surface or to SDS. When the charge of the positive surface was lowered by lysine mutations, the efficiencies of in vitro NTP binding, uridylylation reaction, and unspecific RNA binding were reduced and in vivo the infectivity was debilitated. The most likely uridylylation site, Tyr63, locates to the positively charged surface. Surprisingly, a Tyr63Ala mutation did not prevent replication completely but blocked spreading of the virus. Based on the localization of Tyr119 in the model, it was hypothesized to serve as an alternative uridylylation site. Evidence to support the role of Tyr119 in replication was obtained which gives a positive example of the prediction power of the model. Taken together, our experimental data support the features presented in the model and the idea that the functional diversity is attributable to structural flexibility.     

Linkage of the long QT syndrome to the short arm of chromosome 11: use of five highly polymorphic markers towards more detailed localization of the mutant gene

The long QT syndrome is an autosomally dominantly inherited cardiac disorder characterized by abnormalities of myocardial repolarization, exercise- or stress-related syncopal attacks and risk of sudden death due to cardiac arrhythmias. Genetic linkage studies have defined three LQT loci on chromosomes 11p15.5, 3q21–24 and 7p35–36. We performed linkage analyses in three Finnish LQT families using five amplifiable markers assigned to chromosome 11p15. By multipoint linkage analyses we obtained a maximal lod score of 5.503, suggesting that the LQT1 locus maps between D11S922 and D11S1338 on chromosome 11. Our data provide a step towards closer definition of the exact borderlines of the LQT1 locus in chromosome 11 and demonstrate markers with high utility in identification of gene carriers in the affected families.     

Biogeographical comparison of winter bird assemblages in urban environments in Finland

We studied biogeographical variation of urban bird assemblages in Finland. Winter birds were censused by single-visit study plot method from thirty-one centres of villages or towns along 950 km latitudinal extent. A total twenty-eight bird species was observed and the average density was 61.2 ind./10 ha. The number of dominant species in study areas varied between two and seven and their proportion of the whole assemblage was over 70%. Species richness, but not the density of birds, decreased northwards in pooled data. Higher species richness in south than in north was mainly due to the higher amount of delayed migratory birds (e.g. waterbirds, finches) and southerly distributed bird species. However, in heavily urbanized areas species richness did not decrease northwards. This observation disagreed with the hypothesis that species richness decreased northwards. Bird density, but not species richness, increased with urbanization. In particular, feral pigeon, hooded crow and house sparrow had highest densities in most urbanized areas. As only few bird species are adapted to live in urban areas, species composition and dominant bird species were almost the same in the south and in the north. These urban birds may effectively use energy rich food in feeding tables and overcome the problems of severe climate in the north. This may be the reason why bird species richness does not decrease northwards in urban areas.     

Age-Related Microhabitat Segregation in Willow Tit Parus montanus Winter Flocks

It is expected that through flexibility in behaviour, flock living birds respond to the asymmetries in resource access derived from dominance relationships. We analysed the microhabitat use of willow tits in winter flocks and assessed possible factors which shape habitat segregation between adults and juveniles in different temperature regimes. When foraging in mild conditions (ambient temperature > 0°C), flocks split up into subgroups with adults foraging in inner parts of trees more often than juveniles. However, no differences were recorded in the vertical position occupied in trees. In harsh conditions (< ? 4°C), flocks re‐united and juveniles further moved to outer parts of trees, increasing horizontal segregation between age classes. In mild conditions, vigilance behaviour was not related to the position of birds in trees, but in harsh conditions, scanning frequency was higher in outer parts of trees only for adults. In mild weather, juvenile position in trees was associated with body size and mass. The foraging microhabitat segregation detected in harsh conditions fits the age‐related hoarding distribution previously described in the same population. This supports the hypothesis that hoarded food is important in determining future foraging habitat use. Adult preference and intraspecific competition for safer or richer inner parts of trees as foraging sites during harsh conditions seems to determine the habitat segregation between adults and juveniles. Furthermore, we suggest that in mild weather, when foraging in the absence of adults, juveniles balance the costs of using a potentially dangerous microhabitat with the benefits of building energetically cheap and large food reserves through hoarding. The expected patterns of microhabitat segregation may differ in parids, depending on whether predation risk or other factors such as food availability are the main factors controlling habitat quality.     

The gene encoding human low-molecular weight insulin-like growth-factor binding protein (IGF-BP25): regional localization to 7p12–p13 and description of a DNA polymorphism

The low-molecular weight insulin-like growth-factor binding protein (IGF-BP25) is synthesized by human liver, secretory endometrium and decidua, and is also present in human serum. It binds insulin-like growth factors IGF-I and IGF-II with high affinity, and is proposed to act as a paracrine regulator of cell growth. In situ hybridization studies with a cDNA encompassing the entire protein coding region of IGF-BP25 localized the gene to bands p12-p13 on chromosome 7. Southern blot analysis with the enzyme BglII revealed a common restriction fragment length polymorphism: the presence of the polymorphic BglII site results in the formation of two fragments 4.6 kb and 1.6 kb in size whereas its absence produces a single 6.2 kb fragment. The frequencies of the two alleles were 0.73 and 0.27, respectively. IGF-BP25 constitutes a useful genetic marker for the proximal short arm of chromosome 7.