A biomimetic (titin protein molecular structure) strategy is reported for preparing transparent and healable elastomers featuring supertoughness (345 MJ m ) and high tensile strength (44 MPa) after self-healing enabled by hierarchical (single, double, and quadruple) hydrogen-bonding moieties in the polymer backbone. The rigid domain containing hierarchical H-bonds formed with urethane, urea, and 2-ureido-4[1H]-pyrimidinone groups leads to a durable network structure that has enhanced mechanical properties and is also dynamic for rapid self-healing. Healable polymers with hierarchical hydrogen-bonding interactions show excellent recoverability and high energy dissipation owing to the durable interaction between polymer chains. This biomimetic strategy of using hierarchical hydrogen bonds as building blocks is an alternative approach for obtaining dynamic, strong, yet smart self-healing polymers for heavy-duty protection materials and wearable electronics.

Functional polymer micro- and nanoparticles with novel morphology are of great importance because of their wide range of applications in complex biological systems and nanotechnology. Due to the outstanding advantage of the absence of any surfactant, precipitation polymerization as a heterogeneous polymerization technique has been developed to prepare various uniform and clean polymer particles, such as microspheres, nanoparticles, core-shell particles, core-double shell particles, single-shell hollow particles, double-shell hollow particles, and rattle-type hollow nanostructures. In this review, a general introduction into the categories of precipitation polymerization and their mechanisms is presented. The precise control of particle size, size distribution, pore size, morphology and surface chemistry of micro- and nanoparticles, core-shell hybrids and polymer hollow structures is discussed. The development of complex nanostructures and their applications in separation, drug delivery and nano-reactor systems are highlighted as well.

For a long period of time, scientists studied genomes while assuming they are linear. Recently, chromosome conformation capture (3C)-based technologies, such as Hi-C, have been developed that provide the loci contact frequencies among loci pairs in a genome-wide scale. The technology unveiled that two far-apart loci can interact in the tested genome. It indicated that the tested genome forms a three-dimensional (3D) chromosomal structure within the nucleus. With the available Hi-C data, our next challenge is to model the 3D chromosomal structure from the 3C-derived data computationally. This article presents a deterministic method called ChromSDE, which applies semi-definite programming techniques to find the best structure fitting the observed data and uses golden section search to find the correct parameter for converting the contact frequency to spatial distance. Further, we develop a measure called consensus index to indicate if the Hi-C data corresponds to a single structure or a mixture of structures. To the best of our knowledge, ChromSDE is the only method that can guarantee recovering the correct structure in the noise-free case. In addition, we prove that the parameter of conversion from contact frequency to spatial distance will change under different resolutions theoretically and empirically. Using simulation data and real Hi-C data, we showed that ChromSDE is much more accurate and robust than existing methods. Finally, we demonstrated that interesting biological findings can be uncovered from our predicted 3D structure.

Tumour necrosis factor alpha (TNFα) is a potent cytokine that signals through nuclear factor kappa B (NFκB) to activate a subset of human genes. It is usually assumed that this involves RNA polymerases transcribing responsive genes wherever they might be in the nucleus. Using primary human endothelial cells, variants of chromosome conformation capture (including 4C and chromatin interaction analysis with paired‐end tag sequencing), and fluorescence in situ hybridization to detect single nascent transcripts, we show that TNFα induces responsive genes to congregate in discrete ‘NFκB factories’. Some factories further specialize in transcribing responsive genes encoding micro‐RNAs that target downregulated mRNAs. We expect all signalling pathways to contain this extra leg, where responding genes are transcribed in analogous specialized factories.

The precise splicing of genes confers an enormous transcriptional complexity to the human genome. The majority of gene splicing occurs cotranscriptionally, permitting epigenetic modifications to affect splicing outcomes. Here we show that select exonic regions are demarcated within the three-dimensional structure of the human genome. We identify a subset of exons that exhibit DNase I hypersensitivity and are accompanied by ‘phantom’ signals in chromatin immunoprecipitation and sequencing (ChIP-seq) that result from cross-linking with proximal promoter- or enhancer-bound factors. The capture of structural features by ChIP-seq is confirmed by chromatin interaction analysis that resolves local intragenic loops that fold exons close to cognate promoters while excluding intervening intronic sequences. These interactions of exons with promoters and enhancers are enriched for alternative splicing events, an effect reflected in cell type-specific periexonic DNase I hypersensitivity patterns. Collectively, our results connect local genome topography, chromatin structure and cis-regulatory landscapes with the generation of human transcriptional complexity by cotranscriptional splicing.

Although many long noncoding RNAs (lncRNAs) have been identified in muscle, their physiological function and regulatory mechanisms remain largely unexplored. In this study, we systematically characterized the expression profiles of lncRNAs during C2C12 myoblast differentiation and identified an intronic lncRNA, SYISL (SYNPO2 intron sense-overlapping lncRNA), that is highly expressed in muscle. Functionally, SYISL promotes myoblast proliferation and fusion but inhibits myogenic differentiation. SYISL knockout in mice results in significantly increased muscle fiber density and muscle mass. Mechanistically, SYISL recruits the enhancer of zeste homolog 2 (EZH2) protein, the core component of polycomb repressive complex 2 (PRC2), to the promoters of the cell-cycle inhibitor gene p21 and muscle-specific genes such as myogenin (MyoG), muscle creatine kinase (MCK), and myosin heavy chain 4 (Myh4), leading to H3K27 trimethylation and epigenetic silencing of target genes. Taken together, our results reveal that SYISL is a repressor of muscle development and plays a vital role in PRC2-mediated myogenesis.

We report the development of silica/polymer double-walled hybrid nanotubes, which consist of a hollow cavity, a porous silica inner wall, and a stimuli-responsive (pH, temperature, and redox) polymeric outer wall, as a novel nanocontainer system. The length, diameter, wall thickness, and aspect ratio of the hybrid nanotubes are precisely controlled in the range of 48-506 nm, 41-68 nm, 3-24 nm, and 1.2-7.6, respectively. The hybrid nanotubes loaded with active molecules exhibit morphology-dependent release and pH-, temperature-, redox-responsive release, which enable a wide range of applications from energy storage to drug delivery and self-healing coatings for metal corrosion protection.

A solution-processable graphene oxide (GO)-polymer complex, consisting of GO nanosheets with covalently grafted poly(tert-butyl acrylate) (PtBA) brushes, was prepared via surface-initiated atom transfer radical polymerization (ATRP). The grafted hydrophobic polymer brushes substantially enhance the solubility of GO in organic solvents, and the GO-g-PtBA nanosheets can form a uniform and stable dispersion in toluene. The functionalized GO nanosheets can also be integrated into an electroactive polymer matrix. Bistable electrical conductivity switching behavior and a nonvolatile electronic memory effect were demonstrated in a composite thin film of poly(3-hexylthiophene) (P3HT) containing 5 wt % GO-g-PtBA in an Al/GO-g-PtBA+P3HT/ ITO sandwich structure (ITO ) indium-tin oxide). Hydrolysis of GO-g-PtBA produces water-dispersible GO-g-PAAc (PAAc ) poly(acrylic acid)) nanosheets and allows the preparation of gold nanoparticle-decorated GO-g-PAAc nanofilms from aqueous dispersions.