ABSTRACT
Studies of chemical signals in vertebrates typically target single species; however, a broader understanding of olfactory communication may derive from comparative studies. We collected urine from 12 species representing most families of strepsirrhine primates--an excellent model clade because of variation in scent marking and socioecology. Using SPDE/GC-MS, we identified the volatile chemical composition of male and female urine from six 'urine marking' species and six glandular or 'non-urine marking' species. We found no sex differences, but as predicted, urine markers expressed the most chemically complex and distinctive urine. More distantly related species had more dissimilar urinary profiles, suggesting gradual signal evolution. Reconstructing ancestral chemical profiles revealed different evolutionary trajectories for urine and non-urine markers. We suggest that urine marking is an ancestral behaviour related to solitary, nocturnal living and that parallel evolutionary shifts towards greater reliance on derived glandular marking occurred in a family (Lemuridae) characterized by diurnality and sociality.
Subject(s)
Animal Communication , Phylogeny , Smell/genetics , Strepsirhini/physiology , Animals , Circadian Rhythm , Eliminative Behavior, Animal , Female , Gas Chromatography-Mass Spectrometry , Male , Species Specificity , Strepsirhini/urine , Urine/chemistry , VolatilizationABSTRACT
Helicases separate double-stranded DNA into single-stranded DNA intermediates that are required during replication and recombination. These enzymes are believed to transduce free energy available from ATPase activity to unwind the duplex and translocate along the nucleic acid lattice. The nature of enzyme-substrate interactions between helicases and duplex DNA substrates has not been well-defined. Most helicases require a single-stranded DNA overhang adjacent to duplex DNA in order to initiate unwinding. The strand containing the overhang is referred to as the loading strand whereas the complementary strand is referred to as the displaced strand. We have investigated the interactions between a DNA helicase and the DNA substrate by replacing the displaced strand with a nucleic acid mimic, peptide nucleic acid (PNA). PNA is capable of forming duplex structures with DNA according to Watson-Crick base pairing rules, but contains a N-(2-aminoethyl)glycine backbone in place of the deoxyribose phosphates. The PNA-DNA hybrids had higher melting temperatures than their DNA-DNA counterparts. Dda helicase, from bacteriophage T4, was able to unwind the DNA-PNA substrates at similar rates as DNA-DNA substrates. The results indicate that the rate-limiting step for unwinding is relatively insensitive to the chemical nature of the displaced strand and the thermal stability of oligonucleotide substrates.
Subject(s)
DNA Helicases/chemistry , Viral Proteins , Adenosine Triphosphatases/metabolism , Bacteriophage T4/enzymology , DNA Helicases/metabolism , DNA, Single-Stranded/chemistry , DNA, Viral/chemistry , Enzyme Activation , Hot Temperature , Nucleic Acid Heteroduplexes/chemistry , Oligonucleotides/chemistry , Peptide Nucleic Acids/chemistry , RNA, Viral/chemistry , Substrate SpecificityABSTRACT
In the Asian elephant, wetness akin to perspiration is commonly observed on the cuticles and interdigital areas of the feet; this observation has lead to speculation regarding the existence of an interdigital gland. Our goal was to search for interdigital glands and characterise them morphologically, histochemically, and immunohistochemically. Necropsy samples of interdigital areas from two Asian elephants were obtained. Multiple sections were fixed and processed routinely, then stained with hematoxylin/eosin and differential mucin stains. Immunohistochemistry was also performed for cytokeratins 8 and 10. Interdigital glands resembling human eccrine glands were detected deep within the reticular dermis. Histochemical staining indicated neutral mucopolysaccharides and nonsulphated acid mucopolysaccharides in glandular secretions, and the glandular epithelium also showed immunoreactivity to cytokeratins 8 and 10. Both the histochemical and immunohistochemical staining patterns are analogous to human eccrine structures. This study shows with certainty that Asian elephants possess sweat glands as they are defined histologically.
Subject(s)
Eccrine Glands/anatomy & histology , Elephants/anatomy & histology , Hoof and Claw/anatomy & histology , Animals , Eccrine Glands/chemistry , Eccrine Glands/metabolism , Elephants/physiology , Histocytochemistry/veterinary , Immunohistochemistry/veterinary , Keratins/analysis , Keratins/metabolism , SkinABSTRACT
New analogues of the venerable antimalarial drug primaquine have been synthesized and bioassayed in vivo against Pneumocystis carinii, a life-threatening infection common among immunosuppressed patients. Two of these new compounds are significantly more active than primaquine itself, and provide new information for future drug design and development in this area.
Subject(s)
Antifungal Agents/therapeutic use , Pneumocystis Infections/drug therapy , Primaquine/analogs & derivatives , Primaquine/therapeutic use , Animals , Antifungal Agents/chemical synthesis , Antifungal Agents/chemistry , Antifungal Agents/pharmacology , Dose-Response Relationship, Drug , Drug Design , Female , Humans , Molecular Structure , Pneumocystis/drug effects , Primaquine/chemical synthesis , Primaquine/chemistry , Primaquine/pharmacology , Rats , Structure-Activity RelationshipABSTRACT
GC-MS analysis of extracts from temporal gland secretions of an African elephant has revealed the presence of several farnesol-related sesquiterpenes. Among these are (E)-2, 3-dihydrofarnesol (3), a bumblebee pheromone not seen before in mammals, and a rare component of a Greek tobacco, drimane-8alpha, 11-diol (4), never observed before in an animal.
Subject(s)
Elephants/metabolism , Scent Glands/chemistry , Sesquiterpenes/chemistry , Animals , Farnesol/chemistry , Gas Chromatography-Mass Spectrometry , MaleABSTRACT
Problems were encountered during attempts to prepare N-terminal cysteine-substituted peptide nucleic acids (PNAs) from commercially available, Fmoc-protected monomers. These problems have been surmounted by the use of an S-t-butylmercapto protecting group on the cysteine moiety. The solid-phase syntheses are carried out via a simplified procedure which should be generally useful for manual PNA synthesis.
Subject(s)
Cysteine , Oligodeoxyribonucleotides/chemistry , Peptide Nucleic Acids/chemical synthesis , Base Sequence , Chromatography, High Pressure Liquid , Indicators and Reagents , Oligodeoxyribonucleotides/chemical synthesis , Peptide Nucleic Acids/chemistry , Resins, Plant , Spectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationABSTRACT
In 28 patients the preoperative MR results and arthroscopic examination findings, in which both sides of the rotator cuff were systematically examined, were compared. The interpretive MR criteria were both sensitive and specific for detection of full thickness tears: 100% (5 of 5) and 100% (23 of 23), respectively. Criteria were insensitive in 71% (10 of 14) but specific in 93% (13 of 14) for detection of all tears; 4 of 9 partial thickness tears were not detected of MR. The potential significance of these tears and the use of fat suppression MR sequences to improve detection and depiction of rotator cuff abnormalities are discussed.