De novo deletions and duplications at recombination hotspots in mouse germlines

1. Download : Download high-res image (115KB)
2. Download : Download full-size image

     

Effect of microtubule-associated proteins on the protofilament number of microtubules assembled in vitro

In order to demonstrate the effect of microtubule-associated proteins on the protofilament number of microtubules, we used different systems of microtubule formation in vitro in which these proteins are either functionally eliminated (by DNA or glycerol) or absent (purified tubulin). The results obtained by electron microscopy of ultrathin-sectioned material indicate that under standard conditions in the presence of microtubule-associated proteins microtubules are formed consisting predominantly of 14 protofilaments. In cases of deficiency of microtubule-associated proteins, the mean value of the protofilament number is lower, and the protofilament number within the microtubule population varies remarkably. On the other hand, the action of microtubule-associated proteins is enhanced by histones resulting in increased protofilament numbers. A model is proposed illustrating that the quality and the quantity of microtubule-associated proteins bound to microtubules determine the curvature between the protofilaments and restrict the variety of their binding angles. In this way the microtubule-associated proteins may be regarded as an important factor in determining the structural fidelity of microtubules.     

Reintroducing capercaillie (Tetrao urogallus) into southern Scotland: identification of minimum viable populations at potential release sites

Capercaillie (Tetrao urogallus) populations are declining in western parts of their range, including Scotland. It has been proposed that their numbers, and the extent of their range in Scotland be increased to reduce the risk of a second extinction in the UK. The feasibility of a reintroduction of capercaillie to coniferous plantations in southern Scotland was assessed by undertaking a population viability analysis. Following a review of capercaillie ecology and habitat requirements, VORTEX population simulation software was used to identify a minimum viable population (MVP). From this the minimum dynamic area of suitable habitat required in order to support such a MVP was then calculated. It was estimated that a minimum of 60 individuals would be required in approximately 5000ha of habitat in order for the population to have a >0.95 probability of surviving for 50 years. Supplementation of populations with two unrelated individuals every five years reduced the MVP to ten individuals. Further simulations were run in order to establish the sensitivity of the model to changes in three key parameters. Assessment of areas of suitable habitat identified two potential release sites, Wauchope and Newcastleton forests, in southern Scotland. Some practical considerations relating to management of a release population are outlined. It was concluded that an appropriately planned and resourced reintroduction was feasible.     

Why there are photodamages to photosystem II at low light intensities

An explanation of photodamages to PS II at low light intensities is proposed. The explanation is based on the two following postulates: 1. Intermediate states of the water-oxidizing complex can undergo parasitic reduction to lower degrees of oxidation. 2. Photosynthetic apparatus can minimize the unfavorable effect of such reduction by changes in the number of active reaction centers of PS II. Some steady-state characteristics were calculated under these assumptions. The results obtained show that the frequency of P680 excitations at low light intensities becomes as high as that at saturating light provided that the rate of parasitic reduction is comparable with the rate of the slowest reaction in the cycle of the water- oxidizing complex conversions.     

Prenatal diagnosis of Pallister-Killian syndrome and literature review

Pallister-Killian syndrome (PKS) is a rare sporadic genetic disorder usually caused by mosaicism of an extra isochromosome of 12p (i(12p)). This retrospective study analysed the prenatal ultrasound manifestations and molecular and cytogenetic results of five PKS foetuses. Samples of amniotic fluid and/or cord blood, skin biopsy and placenta were collected. Conventional karyotyping and single nucleotide polymorphism array (SNP array) were performed on all the amniotic fluid or cord blood samples. Copy number variants sequencing (CNV-seq) and fluorescence in situ hybridization (FISH) were also used for the validation for one foetus. All the five foetuses were from pregnancies with advanced parental age. Two foetuses involved structural abnormalities and one foetus had only soft markers, all of which included increased nuchal translucency. The rest two foetuses had normal ultrasounds in the second trimester, which has rarely been reported before. The karyotype revealed typical i(12p) in four cases and a small supernumerary marker chromosome consisting of 12p and 20p in the remaining one case. The proportion of cells with i(12p) ranged from 0 to 100% in cultural cells, while SNP array results suggested 2−4 copies of 12p. For one foetus, metaphase FISH showed normal results, but the interphase FISH suggested cell lines with two, three and four copies of 12p in the amniotic fluid. Advanced parental age may be an important risk factor for PKS, and there were no typical ultrasound manifestations related to PKS. A combination of karyotype analysis and molecular diagnosis is an effective method for the diagnosis of PKS.     

Nucleotide sequence and characterization of a maize cytoplasmic ribosomal protein S11 cDNA

We isolated a Zea mays cDNA encoding the 40S subunit cytoplasmic ribosomal protein S11. The nucleotide sequence was determined and the derived amino acid sequence compared to the corresponding Arabidopsis thaliana protein showing an homology of 90%. This ribosomal protein is encoded by a small multigene family of at least two members. The mRNA steady-state level is about one order of magnitude higher in rapidly growing parts of the plant such as the roots and shoots of seedlings compared to fully expanded leaf tissue.     

Hard-sphere/pseudo-particle modelling (HS-PPM) for efficient and scalable molecular simulation of dilute gaseous flow and transport

Continuum methods are not accurate enough for flows at high Knudsen numbers, whereas rigorous molecular dynamics (MD) methods are too costly for simulations at practical dimensions. Hard-sphere (HS) model is a simplified MD method efficient for dilute gaseous flow but is of poor parallelism due to its event-driven nature, which sets a strong limitation to its large-scale applications. In this work, pseudo-particle modelling, a time-driven modelling approach is coupled with HS model to construct a scalable parallel method capable of simulating flows and transport processes at high Knudsen numbers without losing necessary molecular details in describing their macro-scale behaviours. The method is validated in several classical simulation cases and its performance is evaluated to be favourable. To demonstrate the potential applications of this method, we also simulate the diffusion of small molecules in multi-scale porous media which is related to catalysis, material preparation and micro chemical engineering in the long term.