143 research outputs found

    Decoding of Superimposed Traces Produced by Direct Sequencing of Heterozygous Indels

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    Direct Sanger sequencing of a diploid template containing a heterozygous insertion or deletion results in a difficult-to-interpret mixed trace formed by two allelic traces superimposed onto each other. Existing computational methods for deconvolution of such traces require knowledge of a reference sequence or the availability of both direct and reverse mixed sequences of the same template. We describe a simple yet accurate method, which uses dynamic programming optimization to predict superimposed allelic sequences solely from a string of letters representing peaks within an individual mixed trace. We used the method to decode 104 human traces (mean length 294 bp) containing heterozygous indels 5 to 30 bp with a mean of 99.1% bases per allelic sequence reconstructed correctly and unambiguously. Simulations with artificial sequences have demonstrated that the method yields accurate reconstructions when (1) the allelic sequences forming the mixed trace are sufficiently similar, (2) the analyzed fragment is significantly longer than the indel, and (3) multiple indels, if present, are well-spaced. Because these conditions occur in most encountered DNA sequences, the method is widely applicable. It is available as a free Web application Indelligent at http://ctap.inhs.uiuc.edu/dmitriev/indel.asp

    The impact of model resolution on the simulated Holocene retreat of the southwestern Greenland ice sheet using the Ice Sheet System Model (ISSM)

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    Geologic archives constraining the variability of the Greenland ice sheet (GrIS) during the Holocene provide targets for ice sheet models to test sensitivities to variations in past climate and model formulation. Even as data–model comparisons are becoming more common, many models simulating the behavior of the GrIS during the past rely on meshes with coarse horizontal resolutions (≥10&thinsp;km). In this study, we explore the impact of model resolution on the simulated nature of retreat across southwestern Greenland during the Holocene. Four simulations are performed using the Ice Sheet System Model (ISSM): three that use a uniform mesh and horizontal mesh resolutions of 20, 10, and 5&thinsp;km, and one that uses a nonuniform mesh with a resolution ranging from 2 to 15&thinsp;km. We find that the simulated retreat can vary significantly between models with different horizontal resolutions based on how well the bed topography is resolved. In areas of low topographic relief, the horizontal resolution plays a negligible role in simulated differences in retreat, with each model instead responding similarly to retreat driven by surface mass balance (SMB). Conversely, in areas where the bed topography is complex and high in relief, such as fjords, the lower-resolution models (10 and 20&thinsp;km) simulate unrealistic retreat that occurs as ice surface lowering intersects bumps in the bed topography that would otherwise be resolved as troughs using the higher-resolution grids. Our results highlight the important role that high-resolution grids play in simulating retreat in areas of complex bed topography, but also suggest that models using nonuniform grids can save computational resources through coarsening the mesh in areas of noncomplex bed topography where the SMB predominantly drives retreat. Additionally, these results emphasize that care must be taken with ice sheet models when tuning model parameters to match reconstructed margins, particularly for lower-resolution models in regions where complex bed topography is poorly resolved.</p

    Antarctic Bottom Water Sensitivity to Spatio‐Temporal Variations in Antarctic Meltwater Fluxes

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    Ice sheet melting into the Southern Ocean can change the formation and properties of the Antarctic Bottom Water (AABW). Ocean models often mimic ice sheet melting by adding freshwater fluxes in the Southern Ocean under diverse spatial distributions. We use a global ocean and sea-ice model to explore whether the spatial distribution and magnitude of meltwater fluxes can alter AABW properties and formation. We find that a realistic spatially varying meltwater flux sustains AABW with higher salinities compared to simulations with uniform meltwater fluxes. Finally, we show that increases in ice sheet melting above 12% since 1958 can trigger AABW freshening rates similar to those observed in the Southern Ocean since 1990, suggesting that the increasing Antarctic meltwater discharge can drive the observed AABW freshening

    Protein Phosphatase Magnesium Dependent 1A (PPM1A) Plays a Role in the Differentiation and Survival Processes of Nerve Cells

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    The serine/threonine phosphatase type 2C (PPM1A) has a broad range of substrates, and its role in regulating stress response is well established. We have investigated the involvement of PPM1A in the survival and differentiation processes of PC6-3 cells, a subclone of the PC12 cell line. This cell line can differentiate into neuron like cells upon exposure to nerve growth factor (NGF). Overexpression of PPM1A in naive PC6-3 cells caused cell cycle arrest at the G2/M phase followed by apoptosis. Interestingly, PPM1A overexpression did not affect fully differentiated cells. Using PPM1A overexpressing cells and PPM1A knockdown cells, we show that this phosphatase affects NGF signaling in PC6-3 cells and is engaged in neurite outgrowth. In addition, the ablation of PPM1A interferes with NGF-induced growth arrest during differentiation of PC6-3 cells

    Genomic characteristics of cattle copy number variations

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    <p>Abstract</p> <p>Background</p> <p>Copy number variation (CNV) represents another important source of genetic variation complementary to single nucleotide polymorphism (SNP). High-density SNP array data have been routinely used to detect human CNVs, many of which have significant functional effects on gene expression and human diseases. In the dairy industry, a large quantity of SNP genotyping results are becoming available and can be used for CNV discovery to understand and accelerate genetic improvement for complex traits.</p> <p>Results</p> <p>We performed a systematic analysis of CNV using the Bovine HapMap SNP genotyping data, including 539 animals of 21 modern cattle breeds and 6 outgroups. After correcting genomic waves and considering the pedigree information, we identified 682 candidate CNV regions, which represent 139.8 megabases (~4.60%) of the genome. Selected CNVs were further experimentally validated and we found that copy number "gain" CNVs were predominantly clustered in tandem rather than existing as interspersed duplications. Many CNV regions (~56%) overlap with cattle genes (1,263), which are significantly enriched for immunity, lactation, reproduction and rumination. The overlap of this new dataset and other published CNV studies was less than 40%; however, our discovery of large, high frequency (> 5% of animals surveyed) CNV regions showed 90% agreement with other studies. These results highlight the differences and commonalities between technical platforms.</p> <p>Conclusions</p> <p>We present a comprehensive genomic analysis of cattle CNVs derived from SNP data which will be a valuable genomic variation resource. Combined with SNP detection assays, gene-containing CNV regions may help identify genes undergoing artificial selection in domesticated animals.</p

    Ethiopian indigenous goats offer insights into past and recent demographic dynamics and localadaptation in sub-Saharan African goats

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    Abstract Knowledge on how adaptive evolution and human socio‐cultural and economic interests shaped livestock genomes particularly in sub‐Saharan Africa remains limited. Ethiopia is in a geographic region that has been critical in the history of African agriculture with ancient and diverse human ethnicity and bio‐climatic conditions. Using 52K genome‐wide data analysed in 646 individuals from 13 Ethiopian indigenous goat populations, we observed high levels of genetic variation. Although runs of homozygosity (ROH) were ubiquitous genome‐wide, there were clear differences in patterns of ROH length and abundance and in effective population sizes illustrating differences in genome homozygosity, evolutionary history, and management. Phylogenetic analysis incorporating patterns of genetic differentiation and gene flow with ancestry modelling highlighted past and recent intermixing and possible two deep ancient genetic ancestries that could have been brought by humans with the first introduction of goats in Africa. We observed four strong selection signatures that were specific to Arsi‐Bale and Nubian goats. These signatures overlapped genomic regions with genes associated with morphological, adaptation, reproduction and production traits due possibly to selection under environmental constraints and/or human preferences. The regions also overlapped uncharacterized genes, calling for a comprehensive annotation of the goat genome. Our results provide insights into mechanisms leading to genome variation and differentiation in sub‐Saharan Africa indigenous goats
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