			Home About us Contact

Distinctive Structures (distinctive + structure)

Distribution by Scientific Domains

Life Sciences	50%

Selected Abstracts

At the birth of molecular radiation biology ,

ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, Issue 2-3 2001
Raymond Devoret
Abstract Rational thinking builds on feelings, too. This article starts with a tribute to Richard Setlow, an eminent scientist; it retraces as well some studies in molecular genetics that helped to understand basic questions of radiation biology. In the mid-1950s, the induction of a dormant virus (prophage) by irradiation of its host was an intriguing phenomenon. Soon, it was found that prophage induction results from the inactivation of the prophage repressor. Similarly, a score of induced cellular SOS functions were found to be induced when the LexA repressor is inactivated. Repressor inactivation involves the formation of a newly formed distinctive structure: a RecA-polymer wrapped around single-stranded DNA left by the arrest of replication at damaged sites. By touching this RecA nucleofilament, the LexA repressor is inactivated, triggering the sequential expression of SOS functions. The RecA nucleofilament acts as a chaperone, allowing recombinational repair to occur after nucleotide excision repair is over. The UmuD,C complex, synthesized slowly and parsimoniously, peaks at the end of recombinational repair, ready to be positioned at the tip of a RecA nucleofilament, placing the UmuD,C complex right at a lesion. At this location, UmuD,C prevents recombinational repair, and now acts as an error-prone paucimerase that fills the discontinuity opposite the damaged DNA. Finally, the elimination of lesions from the path of DNA polymerase, allows the resumption of DNA replication, and the SOS repair cycle switches to a normal cell cycle. Environ. Mol. Mutagen. 38:135,143, 2001. © 2001 Wiley-Liss, Inc. [source]

Pharmacotherapy Review: Calcium Channel Blockers

JOURNAL OF CLINICAL HYPERTENSION, Issue 1 2006
Domenic A. Sica MD
As a drug class, calcium channel blockers encompass a heterogeneous group of compounds with distinctive structures and pharmacologic characteristics. These agents are widely used in the treatment of hypertension, chronic coronary ischemia, and/or supraventricular arrhythmias. Much of the early debate alluding to increased cardiovascular risk associated with calcium channel blocker use has been silenced by an array of outcomes trials that show these drugs to be both safe and effective in reducing hard cardiovascular end points. The most common side effects associated with calcium channel blockers are vasodilatory in nature and include a non-volume-dependent form of peripheral edema, flushing, and headache. Despite the sometimes discomforting side effects seen with calcium channel blocker therapy, their robust blood pressure-lowering effect makes them an important component of most multidrug regimens used for blood pressure control. [source]

Molecular diversity of the genetic loci responsible for lipopolysaccharide core oligosaccharide assembly within the genus Salmonella

MOLECULAR MICROBIOLOGY, Issue 5 2002
Natalia A. Kaniuk
Summary The waa locus on the chromosome of Salmonella enterica encodes enzymes involved in the assembly of the core oligosaccharide region of the lipopolysaccharide (LPS) molecule. To date, there are two known core structures in Salmonella, represented by serovars Typhimurium (subspecies I) and Arizonae (subspecies IIIA). The waa locus for serovar Typhimurium has been characterized. Here, the corresponding locus from serovar Arizonae is described, and the molecular basis for the distinctive structures is established. Eleven of the 13 open reading frames (ORFs) are shared by the two loci and encode conserved proteins of known function. Two polymorphic regions distinguish the waa loci. One involves the waaK gene, the product of which adds a terminal ,-1,2-linked N -acetylglucosamine residue that characterizes the serovar Typhimurium core oligosaccharide. There is an extensive internal deletion within waaK of serovar Arizonae. The serovar Arizonae locus contains a novel ORF (waaH) between the waaB and waaP genes. Structural analyses and in vitro glycosyltransferase assays identified WaaH as the UDP-glucose:(glucosyl) LPS ,-1,2-glucosyltransferase responsible for the addition of the characteristic terminal glucose residue found in serovar Arizonae. Isolates comprising the Salmonella Reference Collections, SARC (representing the eight subspecies of S. enterica) and SARB (representing subspecies I), were examined to assess the distribution of the waa locus polymorphic regions in natural populations. These comparative studies identified additional waa locus polymorphisms, shedding light on the genetic basis for diversity in the LPS core oligosaccharides of Salmonella isolates and identifying potential sources of further novel LPS structures. [source]

A new psittaciform bird from the London Clay (Lower Eocene) of England

PALAEONTOLOGY, Issue 2 2000
Gareth J. Dyke
A new psittaciform bird from the Lower Eocene (Ypresian) London Clay of England is described. This taxon, Pulchrapollia gracilis gen. et sp. nov., is assigned to the order Psittaciformes (parrots) on the basis of several distinctive structures of the tarsometatarsus, namely the trochlea for metatarsal III (trochlea metatarsi III) bearing a tubercle on its lateral side and the trochlea for metatarsal IV (trochlea metatarsi IV) completely retroverted (fully zygodactyl foot). Comparisons with other fossil and Recent taxa further support this conclusion. Cladistic analysis shows that Pulchrapollia is the sister-taxon of the single extant family within Psittaciformes, the Psittacidae. Palaeopsittacus georgei, a taxon previously described from the London Clay, is most likely based on some unassociated material and is regarded here as incertae sedis. [source]