Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa.

The autosomal dominant retinitis pigmentosa (RP) locus, designated RP1, has been mapped through linkage studies to a 4-cM interval at 8q11-13. Here we describe a new photoreceptor-specific gene that maps in this interval and whose expression is modulated by retinal oxygen levels in vivo. This gene consists of at least 4 exons that encode a predicted protein of 2,156 amino acids. A nonsense mutation at codon 677 of this gene is present in approximately 3% of cases of dominant RP in North America. We also detected two deletion mutations that cause frameshifts and introduce premature termination codons in three other families with dominant RP. Our data suggest that mutations in this gene cause dominant RP, and that the encoded protein has an important but unknown role in photoreceptor biology.     

sBLM味觉物质生物敏感器件的研究

本文研究以琼脂糖为基的固体支撑双层脂膜（ｓＢＬＭ）对味觉物质（乙酸、盐酸喹咛、蔗糖）的响应．这三种味觉物质显著地改变了膜电位，盐酸喹咛、蔗糖对膜电阻有一定影响，脂膜对乙酸和盐酸喹咛也有良好的线性响应．检测灵敏度分别为１２μｍｏｌ／Ｌ和１．３μｍｏｌ／Ｌ，其响应特性、检测灵敏度都达到或优于现有的其它检测方法．用Ｃ６０修饰卵磷脂双层脂膜，加大了膜强度，用它检测上述三种物质，得到了相同结果．     

光学头定位系统的输入成形控制

光学头定位控制由于快速性的要求使得系统产生振荡,影响定位精度.本文应用输入成形方法抑制光头在定位时的振动.通过建立光学头机电系统的数学模型,对于无参数摄动和有参数摄动两种情形分别应用零振荡()和零振荡加微分()两种输入成形控制器进行振动抑制,计算机数值仿真结果表明,该方法对于抑制光学头定位过程中的振动具有较好的效果.     

Distortion of proximodistal information causes JNK-dependent apoptosis in Drosophila wing.

Distinct and evolutionarily conserved signal-transduction cascades mediate the survival or death of cells during development. The c-Jun amino-terminal kinases (JNKs) of the mitogen-activated protein kinase superfamily are involved in apoptotic signalling in various cultured cells. However, the role of the JNK pathway in development is less well understood. In Drosophila, Decapentaplegic (Dpp; a homologue of transforming growth factor-beta) and Wingless (Wg; a Wnt homologue) proteins are secretory morphogens that act cooperatively to induce formation of the proximodistal axis of appendages. Here we show that either decreased Dpp signalling in the distal wing cells or increased Dpp signalling in the proximal wing cells causes apoptosis. Inappropriate levels of Dpp signalling lead to aberrant morphogenesis in the respective wing zones, and these apoptotic zones are also determined by the strength of the Wg signal. Our results indicate that distortion of the positional information determined by Dpp and Wg signalling gradients leads to activation of the JNK apoptotic pathway, and the consequent induction of cell death thereby maintains normal morphogenesis.     

HCO-3-ATPase activity distribution in rat liver cell fractions prepared by zonal centrifugation.

Plasma membrane sheets prepared by zonal centrifugation of a premicrosomal pellet obtained from a rat liver homogenate are devoid of HCO-3-ATPase activity. Since the microsomal fraction is also lacking in this ATPase activity, it can be concluded that the HCO-3-ATPase is not involved in the secretion of HCO-3 into bile.     

Distribution and first reports of Branchiobdellida (Annelida: Clitellata) on crayfish in the prairie provinces of Canada

Orconectes virilis (northern crayfish) were collected from 67 sites in Alberta, Saskatchewan, Manitoba, and far-western Ontario, Canada, and yielded 2 species of branchiobdellidans, Cambarincola vitreus and Cambarincola chirocephalus. This is the first report of branchiobdellidans in the Prairie Provinces. Cambarincola vitreus was distributed across the study area, but C. chirocephalus appeared to be restricted to southeastern Saskatchewan, southern Manitoba, and the site in western Ontario. Neither branchiobdellidan species was observed on crayfish in the Beaver River or the South Saskatchewan River and associated tributaries upstream (west) of Saskatoon, Saskatchewan, despite multiple sampling at these locations.     

Vaspin inhibits kallikrein 7 by serpin mechanism

The molecular target of the adipokine vaspin (visceral adipose tissue-derived serpin; serpinA12) and its mode of action are unknown. Here, we provide the vaspin crystal structure and identify human kallikrein 7 (hK7) as a first protease target of vaspin inhibited by classical serpin mechanism with high specificity in vitro. We detect vaspin–hK7 complexes in human plasma and find co-expression of both proteins in murine pancreatic β-cells. We further demonstrate that hK7 cleaves human insulin in the A- and B-chain. Vaspin treatment of isolated pancreatic islets leads to increased insulin concentration in the media upon glucose stimulation without influencing insulin secretion. By application of vaspin and generated inactive mutants, we find the significantly improved glucose tolerance in C57BL/6NTac and db/db mice treated with recombinant vaspin fully dependent on the vaspin serpin activity and not related to vaspin-mediated changes in insulin sensitivity as determined by euglycemic-hyperinsulinemic clamp studies. Improved glucose metabolism could be mediated by increased insulin plasma concentrations 150 min after a glucose challenge in db/db mice, supporting the hypothesis that vaspin may inhibit insulin degradation by hK7 in the circulation. In conclusion, we demonstrate the inhibitory serpin nature and the first protease target of the adipose tissue-derived serpin vaspin, and our findings suggest hK7 inhibition by vaspin as an underlying physiological mechanism for its compensatory actions on obesity-induced insulin resistance.