Entropic Bristles Tune the Seeding Efficiency of Prion-Nucleating Fragments

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Bristles induce bracts via the EGFR pathway on Drosophila legs

A long-standing mystery in Drosophila has been: how do certain bristles induce adjacent cells to make bracts (a type of thick hair) on their proximal side? The apparent answer, based on loss- and gain-of-function studies, is that they emit a signal that neighbors then transduce via the epidermal growth factor receptor pathway. Suppressing this pathway removes bracts, while hyperactivating it evokes bracts indiscriminately on distal leg segments. Misexpression of the diffusible ligand Spitz (but not its membrane-bound precursor) elicits extra bracts at normal sites. What remains unclear is how a secreted signal can have effects in one specific direction.     

山羊毛提取L-胱氨酸杂质源及其除杂工艺

山羊毛提取L 胱氨酸过程中伴有上百种有机类、无机类杂质的形成 ,分析杂质的形成过程及其对胱氨酸收率和产品质量的影响 ,采用料毛物理化学法除杂、活性炭两次脱色、三次中和重结晶除杂工艺 ,杂质除净率高 ,L 胱氨酸产品质量达HG 2 0 30 - 91优质品标准。     

Silicon Deposition in the Inflorescence Bristles and Macrohairs of Setaria italica (L.) Beauv.

Silicon deposits in the inflorescence bristles subtending eachspikelet, and in the macrohairs of foxtail millet (Setaria italica(L.) Beauv.) were investigated using scanning electron microscopyand electron-probe microanalysis. High concentrations of silicon were detected in the pricklehairs which covered the bristles. In the unicellular macrohairscovering the inflorescence axis and its branches, silicon wasdeposited along the whole length of the hairs. The mechanisms by which silicification may have taken place,and the possibility that the bristles and macrohairs are involvedin the aetiology of oesophageal cancer in N. China are discussed. Setaria italica (L.) Beauv., foxtail millet, millet, silicon deposits, silicification, prickle hairs, scanning electron microscopy, electron-probe microanalysis     

Bristles before down: A new perspective on the functional origin of feathers

Over the course of the last two decades, the understanding of the early evolution of feathers in nonavian dinosaurs has been revolutionized. It is now recognized that early feathers had a simple form comparable in general structure to the hairs of mammals. Insight into the prevalence of simple feathers throughout the dinosaur family tree has gradually arisen in tandem with the growing evidence for endothermic dinosaur metabolisms. This has led to the generally accepted opinion that the early feather coats of dinosaurs functioned as thermo insulation. However, thermo insulation is often erroneously stated to be a likely functional explanation for the origin of feathers. The problem with this explanation is that, like mammalian hair, simple feathers could serve as insulation only when present in sufficiently high concentrations. The theory therefore necessitates the origination of feathers en masse. We advocate for a novel origin theory of feathers as bristles. Bristles are facial feathers common among modern birds that function like mammalian tactile whiskers, and are frequently simple and hair‐like in form. Bristles serve their role in low concentrations, and therefore offer a feasible first stage in feather evolution.     

Identification of a 41 kDa Protein Embedded in the Biosilica of Scales and Bristles Isolatedfrom Mallomonas splendens (Synurophyceae, Ochrophyta)

Cells of the photosynthetic protist Mallomonas splendens (Synurophyceae, Ochrophyta) are encased within a highly patterned wall or scale case that consists of silicified scales and bristles. In an effort to understand the mechanisms that unicellular protists utilize to produce elaborate, mineralized structures of great complexity and hierarchical structure, we identified and characterized a 41 kDa protein from purified scales/bristles isolated from M. splendens (SP41 for Scale Protein of 41 kDa). A cDNA encoding this protein was isolated and sequence analysis indicated that it is a novel protein. Polyclonal antibodies were generated against bacterially expressed SP41 and used to localize the protein throughout scale and bristle morphogenesis. Immunoelectron microscopy confirmed the biochemical data that SP41 is a component of mature scales and bristles, the protein localizing to silicified components of the purified extracellular matrix. During scale and bristle biogenesis within the cell, SP41 is deposited into a specialized Silica Deposition Vesicle (SDV) concomitant with silica deposition, a highly regulated event during scale and bristle formation. These results argue for SP41 playing a role in morphogenesis and/or silicification within the SDV during scale and bristle biogenesis.