PTC124 targets genetic disorders caused by nonsense mutations

Nonsense mutations promote premature translational termination and cause anywhere from 5-70% of the individual cases of most inherited diseases. Studies on nonsense-mediated cystic fibrosis have indicated that boosting specific protein synthesis from <1% to as little as 5% of normal levels may greatly reduce the severity or eliminate the principal manifestations of disease. To address the need for a drug capable of suppressing premature termination, we identified PTC124-a new chemical entity that selectively induces ribosomal readthrough of premature but not normal termination codons. PTC124 activity, optimized using nonsense-containing reporters, promoted dystrophin production in primary muscle cells from humans and mdx mice expressing dystrophin nonsense alleles, and rescued striated muscle function in mdx mice within 2-8 weeks of drug exposure. PTC124 was well tolerated in animals at plasma exposures substantially in excess of those required for nonsense suppression. The selectivity of PTC124 for premature termination codons, its well characterized activity profile, oral bioavailability and pharmacological properties indicate that this drug may have broad clinical potential for the treatment of a large group of genetic disorders with limited or no therapeutic options.     

Msh2 deficiency prevents in vivo somatic instability of the CAG repeat in Huntington disease transgenic mice

Huntington disease (HD), an autosomal dominant, progressive neurodegenerative disorder, is caused by an expanded CAG repeat sequence leading to an increase in the number of glutamine residues in the encoded protein. The normal CAG repeat range is 5-36, whereas 38 or more repeats are found in the diseased state; the severity of disease is roughly proportional to the number of CAG repeats. HD shows anticipation, in which subsequent generations display earlier disease onsets due to intergenerational repeat expansion. For longer repeat lengths, somatic instability of the repeat size has been observed both in human cases at autopsy and in transgenic mouse models containing either a genomic fragment of human HD exon 1 (ref. 9) or an expanded repeat inserted into the endogenous mouse gene Hdh (ref. 10). With increasing repeat number, the protein changes conformation and becomes increasingly prone to aggregation, suggesting important functional correlations between repeat length and pathology. Because dinucleotide repeat instability is known to increase when the mismatch repair enzyme MSH2 is missing, we examined instability of the HD CAG repeat by crossing transgenic mice carrying exon 1 of human HD (ref. 16) with Msh2-/- mice. Our results show that Msh2 is required for somatic instability of the CAG repeat.     

Influence of 2-methyl-2-(p-1,2,3,4-tetrahydro-1-naphthylphenoxy)propionic acid on the oxidation of cholesterol by rat liver mitochondria

Zusammenfassung Es wird gezeigt, dass bei männlichen Wistar-Ratten im 3-Wochen-Diätexperiment mit Zusatz von 0,3% 2-Methyl-2-(p-1,2,3,4-Tetrahydro-1-naphthylphenoxy)-Propionsäure (Su-13437) die Oxydation von 26-¹⁴C-Cholesterin zu¹⁴CO₂ durch Lebermitochondrien (bezogen auf mg/N) ähnlich wie bei den Kontrollen war. Bei den Versuchstieren war jedoch bei Abwesenheit von Cytosol im System die Oxydation durch Lebermitochondrien erhöht.

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Acknowledgment. This work was supported, in part, by a grant No. HE-03299 and a Research Career Award No. 4-K6-HE-0734 from the National Heart Institute, N.I.H. We are indebted to Dr. W. I.Taylor, CIBA Pharmaceutical Co., Summit, N.J., for the generous gift of Su-13,437.     

Comprehensive list by habitat of algae of Utah, USA.

A list of the algal species that have been reported from the state of Utah is presented. Also listed are the habitats from which these algae were collected. A total of nearly 1,900 taxa have been identified to the species level or below. Diatoms comprise the largest group, with nearly 1,000 taxa, followed by the green algae with over 550 taxa.     

基于科学思维的英语文学教学:跨学科的视角

本文阐述基于科学思维过程的英语文学教学策略,即英语文学作品以综合课程的形式应用于教学实践活动.其要点是从优秀文学作品中选取需要解决问题的情境,从跨学科的视角来审视作品中的矛盾和冲突.教师们通过分析这些问题情境教给学生科学的思维方法.其教学策略的重点在于提出问题和做出决策.这些用于跨学科教学策略的文学作品是关注真实世界的起点.生活中面临的两难问题通过基于科学思维的文学教学而获得理性的解释或合理的解决.     

Evidence for an olfactory receptor which responds to nicotine--nicotine as an odorant

The tobacco alkaloid (S)(-)-nicotine, when applied as a vapour to an in vitro head preparation, stimulates the olfactory epithelium in three strains of rats and to a lesser extent in two strains of mice. The electro-olfactogram (EOG) generated by nicotine has similar characteristics to the EOGs produced by known odorants. The nicotine EOG increases with increasing concentration of nicotine vapour (1-100 nM) applied to the olfactory epithelium. Differential reduction of the nicotine EOG by the lectin concanavalin A is seen in Wistar and Lister Hooded rats. The reduction of the nicotine EOG by concanavalin A is prevented by adding alpha-methyl-D-mannoside to the lectin superfusion medium. This suggests that there is a glyco-moiety associated with at least one olfactory receptor responding to nicotine. Our results suggest that rat olfactory epithelium has receptor sites for nicotine. Nicotine is an unusual compound because it shows both odorant and pharmacological properties.     

Influence of pyridinolcarbamate on hepatic cholesterogenesis in rats

Zusammenfassung Männliche Wistar-Ratten wurden während 3 Wochen mit 0,3% Pyridinolcarbamat gefüttert, der Cholesterinspiegel in Leber und Serum bestimmt und ausserdem der Einbau von Na-Acetat-1-¹⁴C und Mevalonsäure-2-¹⁴C im Cholesterin von Leberschnitten gemessen. Der Cholesterinspiegel in Serum und Leber wird durch Pyridinolcarbamat nicht beeinflusst. Der Einbau von Acetat-1-¹⁴C in Cholesterin wurde durch Pyridinolcarbamat gehemmt, während die Conversion von Mevalonat-2-¹⁴C unbeeinflusst blieb.     

Impaired hydroxylation of 5-methylcytosine in myeloid cancers with mutant TET2

TET2 is a close relative of TET1, an enzyme that converts 5-methylcytosine (5mC) to 5-hydroxymethylcytosine (5hmC) in DNA. The gene encoding TET2 resides at chromosome 4q24, in a region showing recurrent microdeletions and copy-neutral loss of heterozygosity (CN-LOH) in patients with diverse myeloid malignancies. Somatic TET2 mutations are frequently observed in myelodysplastic syndromes (MDS), myeloproliferative neoplasms (MPN), MDS/MPN overlap syndromes including chronic myelomonocytic leukaemia (CMML), acute myeloid leukaemias (AML) and secondary AML (sAML). We show here that TET2 mutations associated with myeloid malignancies compromise catalytic activity. Bone marrow samples from patients with TET2 mutations displayed uniformly low levels of 5hmC in genomic DNA compared to bone marrow samples from healthy controls. Moreover, small hairpin RNA (shRNA)-mediated depletion of Tet2 in mouse haematopoietic precursors skewed their differentiation towards monocyte/macrophage lineages in culture. There was no significant difference in DNA methylation between bone marrow samples from patients with high 5hmC versus healthy controls, but samples from patients with low 5hmC showed hypomethylation relative to controls at the majority of differentially methylated CpG sites. Our results demonstrate that Tet2 is important for normal myelopoiesis, and suggest that disruption of TET2 enzymatic activity favours myeloid tumorigenesis. Measurement of 5hmC levels in myeloid malignancies may prove valuable as a diagnostic and prognostic tool, to tailor therapies and assess responses to anticancer drugs.     

基于能量原理和Kalman滤波器的实时模型修正策略

为了实时监测结构的安全状态,提出了一种计算速度快、易收敛的模型修正策略.首先通过计算瞬时能量来建立结构单元刚度和结构响应之间的关系;然后,将结构瞬时能量代入Kalman滤波器中,根据每一时间步能量预测值和实际测量值的差异进行修正,得到结构的真实刚度;最后,以美国地震工程模拟中心数据库(NEES)中的美国某州际公路指示牌支撑桁架为例进行数值验证,结果表明:无噪声干扰情况下,刚度发生20%,40%,60%,80%损伤的杆件和未发生损伤的杆件均能在0.4 s内从初始刚度收敛到各自的真实刚度;在5%随机噪声干扰下,利用该策略修正得到的刚度误差均小于12%;每一时间步所消耗的CPU时间远小于采样周期.因此,利用能量原理和Kalman滤波器能够快速有效地对未知刚度的结构进行实时模型修正.