Mesenchymal stem cells within tumour stroma promote breast cancer metastasis

Mesenchymal stem cells have been recently described to localize to breast carcinomas, where they integrate into the tumour-associated stroma. However, the involvement of mesenchymal stem cells (or their derivatives) in tumour pathophysiology has not been addressed. Here, we demonstrate that bone-marrow-derived human mesenchymal stem cells, when mixed with otherwise weakly metastatic human breast carcinoma cells, cause the cancer cells to increase their metastatic potency greatly when this cell mixture is introduced into a subcutaneous site and allowed to form a tumour xenograft. The breast cancer cells stimulate de novo secretion of the chemokine CCL5 (also called RANTES) from mesenchymal stem cells, which then acts in a paracrine fashion on the cancer cells to enhance their motility, invasion and metastasis. This enhanced metastatic ability is reversible and is dependent on CCL5 signalling through the chemokine receptor CCR5. Collectively, these data demonstrate that the tumour microenvironment facilitates metastatic spread by eliciting reversible changes in the phenotype of cancer cells.     

Tundra vegetation of three cirque basins in the northern San Juan Mountains, Colorado

The vegetation of three alpine cirque basins in the northern San Juan Mountains of southwestern Colorado was inventoried and analyzed for the degree of specificity shown by vascular plant communities for certain types of habitats identified as representative of the basins. A total of 197 vascular plant species representing 31 families was inventoried. Growth forms of all species were noted and a growth form spectrum for all of the communities was derived. The caespitose monocot and erect dicot growth forms are the most important growth forms among the community dominants. The most common growth form among all species is the rosette dicot.           

Spring waterfowl migration in the Uinta Basin of northeastern Utah

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Alpine vascular flora of the Ruby Range, West Elk Mountains, Colorado

The Ruby Range is a northern extension of the West Elk Mountains of west central Colorado. Composed primarily of sedimentary rocks, the range is heavily faulted and intruded by many dikes and sills. Eight study areas, selected as representative of the major topographic features of the range, were analyzed floristically. A vascular flora of 220 species in 111 genera and 35 families is reported. The phytogeographic distribution of the flora is primarily alpine and western North American. The flora of the Ruby Range shows a 74% similarity to the flora of the San Juan Mountains to the southwest.     

Factors influencing selection of road culverts as winter roost sites by Western Burrowing Owls

The conversion of coastal prairie to farmland in southern Texas has drastically reduced the number of available animal burrows, thereby forcing western Burrowing Owls ( Athene cunicularia hypugaea ) wintering in southern Texas to use nontraditional roost sites such as roadside culverts. We studied factors influencing the selection of road culverts as roost sites by Burrowing Owls by comparing characteristics of 34 occupied and 100 unoccupied culverts. All occupied culverts were in agricultural habitat. Culverts with small diameters (≤16 cm) and those with an east–west orientation were occupied by Burrowing Owls in greater proportions than were culverts with larger diameters or different orientations. Occupied culverts were also associated with absence of grass, absence of woody vegetation, and presence of crop stubble. Our results provide guidelines for making drainage culverts more attractive to Burrowing Owls, but use of roadside culverts by Burrowing Owls may expose the owls to an increased risk of mortality from vehicle collisions. To avoid this dilemma, our guidelines for culverts could also be adapted as criteria for installation of artificial burrows in habitats suitable for wintering Burrowing Owls.     

Chemical explanation and physical dynamics: Two research schools at the First Solvay chemistry conferences, 1922–1928

The convening of the first three Solvay Chemistry Conferences in Brussels from 1922–1928 marked an important turning point for the discipline of chemistry. Whereas much of nineteenth-century chemical endeavour had focused on compositional and functional analysis of chemical compounds, many leaders in chemistry were turning to questions of molecular dynamics by the early twentieth century. Two competing schools of chemical dynamics, which were represented at the Solvay Conferences, were a predominantly English group (Lowry, Lapworth, Robinson, Ingold) who worked out electron and ionic interpretations of organic reaction mechanisms, and a French group (Perrin, Job) who developed a generalized radiation hypothesis of reaction activation. While differences in conceptual and stylistic approach separated the two schools, they agreed on the need to apply contemporary physical theory to old chemical problems, and to develop a theoretical chemistry complementary to theoretical physics.     

Genome assembly comparison identifies structural variants in the human genome

Numerous types of DNA variation exist, ranging from SNPs to larger structural alterations such as copy number variants (CNVs) and inversions. Alignment of DNA sequence from different sources has been used to identify SNPs and intermediate-sized variants (ISVs). However, only a small proportion of total heterogeneity is characterized, and little is known of the characteristics of most smaller-sized (<50 kb) variants. Here we show that genome assembly comparison is a robust approach for identification of all classes of genetic variation. Through comparison of two human assemblies (Celera's R27c compilation and the Build 35 reference sequence), we identified megabases of sequence (in the form of 13,534 putative non-SNP events) that were absent, inverted or polymorphic in one assembly. Database comparison and laboratory experimentation further demonstrated overlap or validation for 240 variable regions and confirmed >1.5 million SNPs. Some differences were simple insertions and deletions, but in regions containing CNVs, segmental duplication and repetitive DNA, they were more complex. Our results uncover substantial undescribed variation in humans, highlighting the need for comprehensive annotation strategies to fully interpret genome scanning and personalized sequencing projects.     

In germ cells of mouse embryonic ovaries, the decision to enter meiosis precedes premeiotic DNA replication

The transition from mitosis to meiosis is a defining juncture in the life cycle of sexually reproducing organisms. In yeast, the decision to enter meiosis is made before the single round of DNA replication that precedes the two meiotic divisions. We present genetic evidence of an analogous decision point in the germ line of a multicellular organism. The mouse Stra8 gene is expressed in germ cells of embryonic ovaries, where meiosis is initiated, but not in those of embryonic testes, where meiosis does not begin until after birth. Here we report that in female embryos lacking Stra8 gene function, the early, mitotic development of germ cells is normal, but these cells then fail to undergo premeiotic DNA replication, meiotic chromosome condensation, cohesion, synapsis and recombination. Combined with previous findings, these genetic data suggest that active differentiation of ovarian germ cells commences at a regulatory point upstream of premeiotic DNA replication.     

Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation

Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation (LBSL) has recently been defined based on a highly characteristic constellation of abnormalities observed by magnetic resonance imaging and spectroscopy. LBSL is an autosomal recessive disease, most often manifesting in early childhood. Affected individuals develop slowly progressive cerebellar ataxia, spasticity and dorsal column dysfunction, sometimes with a mild cognitive deficit or decline. We performed linkage mapping with microsatellite markers in LBSL families and found a candidate region on chromosome 1, which we narrowed by means of shared haplotypes. Sequencing of genes in this candidate region uncovered mutations in DARS2, which encodes mitochondrial aspartyl-tRNA synthetase, in affected individuals from all 30 families. Enzyme activities of mutant proteins were decreased. We were surprised to find that activities of mitochondrial complexes from fibroblasts and lymphoblasts derived from affected individuals were normal, as determined by different assays.