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“Previously, bacteria were found using metagenomics or microbiome sequencing, and now we have confirmed that signal based on our ability to label the bacterial RNA with a florescent ‘tag’ and actually see them,” said Dr. Maxim Seferovic, instructor in obstetrics and gynecology at Baylor and lead author in the study. “We leveraged a powerful new imaging technology to add greater specificity in the signal of bacterial RNA, which helped us to see bacteria within the microarchitecture of the placental tissue.”

Researchers examined microbes in term and preterm gestations using a signal amplified 16S universal in situ hybridization probe designed for bacterial rRNA, along with several other histologic methods. Seferovic said the study was carefully designed to control for contamination as best as possible, so that these sparse bacteria could be accurately attributed to their location in the placenta.

“We did not see quantitative or numerical differences between preterm or full-term births, nor did we see them localizing to different substrata. But we do see differences in what genera of bacteria are there in preterm or full term, and this supported our and other’s past findings as well,” said Aagaard.

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Knowledge of the kinds and numbers of nuclear point mutations in human tissues is essential to the understanding of the mutation mechanisms underlying genetic diseases. However, nuclear point mutant fractions in normal humans are so low that few methods exist to measure them. We have now developed a means to scan for point mutations in 100 bp nuclear single copy sequences at mutant fractions as low as 10–6.Beginning with about 10 human cells we first enrich for the desired nuclear sequence 10 000-fold from the genomic DNA by sequence-specific hybridization coupled with a biotin–streptavidin capture system. We next enrich for rare mutant sequences 100-fold against the wild-type sequence by wide bore constant denaturant capillary electrophoresis (CDCE). The mutant-enriched sample is subsequently amplified by high fidelity PCR using fluorescein-labeled primers. Amplified mutant sequences are further enriched via two rounds of CDCE coupled with high fidelity PCR. Individual mutants, seen as distinct peaks on CDCE, are then isolated and sequenced. We have tested this approach by measuring N-methyl–N ′-nitro–N-nitrosoguanidine (MNNG)-induced point mutations in a 121 bp sequence of the adenomatous polyposis coli gene (APC) in human lymphoblastoid MT1 cells. Twelve different MNNG-induced GC→AT transitions were reproducibly observed in MNNG-treated cells at mutant fractions between 2 × 10–6 and 9 × 10–6. The sensitivity of this approach was limited by the fidelity of Pfu DNA polymerase, which created 14 different GC→TA transversions at a mutant fraction equivalent to ~10–6 in the original samples. The approach described herein should be general for all DNA sequences suitable for CDCE analysis. Its sensitivity and capacity would permit detection of stem cell mutations in tissue sectors consisting of ~10 cells.

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A research group from RIKEN and Kyushu University has developed a new type of material, based on ethylene, which exhibits a number of useful properties such as self-healing and shape memory. Remarkably, some of the materials can spontaneously self-heal even in water or acidic and alkali solutions. The new material is based on ethylene, a compound that is the source of much of the plastic in use today.

Materials that can self-heal have become a popular area of research during the last decade, and a variety of materials have been developed. However, most of the materials reported to date have relied on sophisticated designs that incorporate chemical mechanisms into polymer networks, such as irreversible or reversible covalent-bond formation, hydrogen bonding, metal-ligand interactions, or ionic interactions. As a result, they require some , such as heat or pressure, to prompt them to heal, and in most cases, they do not function in water, acid or alkaline solutions because the chemical networks cannot survive such conditions. The ideal is to create a material that possesses sufficient toughness and can autonomously self-heal under various conditions.

For the present research, published in the Journal of the American Chemical Society, the researchers used a catalyst based on scandium, a rare metal, to create polymers composed of alternating sequences of ethylene and anisylpropylenes and shorter ethylene-ethylene segments by the of ethylene and anisylpropylenes. This new class of well-defined, functionalized polyolefins ranged from soft viscoelastic materials—materials that can be both elastic but also exhibit liquid-like properties—to tough elastomers, which can be stretched but return to their original shapes, and rigid plastics. The elastomer copolymers were very elastic, and tough, and also showed remarkable self-healing property, as they autonomously self-healed when subjected to mechanical damage not only in a dry environment but also in water and aqueous acid and alkaline solutions, without the need for any external energy or stimulus.

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Ever wonder why some fortunate people eat chips, don’t exercise, and still don’t get clogged arteries? It could be because they’ve got lucky genes.

Now Alphabet (Google’s parent company) is bankrolling a startup company that plans to use gene editing to spread fortunate DNA variations with “one-time” injections of the gene-editing tool CRISPR.

Heart doctors involved say the DNA-tweaking injections could “confer lifelong protection” against heart disease.

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In the spirit of ideas worth spreading, TEDx is a program of local, self-organized events that bring people together to share a TED-like experience. At a TEDx event, TEDTalks video and live speakers combine to spark deep discussion and connection in a small group. These local, self-organized events are branded TEDx, where x = independently organized TED event. The TED Conference provides general guidance for the TEDx program, but individual TEDx events are self-organized.* (*Subject to certain rules and regulations)

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